Contract Manufacturing

Aesica Pharmaceuticals-Custom Synthesis, API and Finished Dosage Form Supplies

Our API development chemists can carry out all your process development.
Our API development chemists can carry out all your process development.
Aesica has been supplying bulk APIs to the global pharmaceutical industry for over 25 years.
Aesica has been supplying bulk APIs to the global pharmaceutical industry for over 25 years.
Aesica also offers finished dosage forms.
Aesica also offers finished dosage forms.
We offer method development and validation in compliance with ICH to support all your IND/CMC requirements.
We offer method development and validation in compliance with ICH to support all your IND/CMC requirements.
We have two pilot plants for early phase process development.
We have two pilot plants for early phase process development.

American Regent (Luitpold)-Pharmaceutical Contract Manufacturing

American Regent’s mission is to bring the highest quality products to the global healthcare community.
American Regent’s mission is to bring the highest quality products to the global healthcare community.
We have specialized in the manufacture of sterile injectable pharmaceuticals since 1967.
We have specialized in the manufacture of sterile injectable pharmaceuticals since 1967.
We are involved in every step of the manufacturing process - from the testing of raw materials through to labeling, packaging and delivery of the finished product.
We are involved in every step of the manufacturing process - from the testing of raw materials through to labeling, packaging and delivery of the finished product.
All American Regent products are manufactured at our innovative, state-of-the-art cGMP facility in Shirley, New York.
All American Regent products are manufactured at our innovative, state-of-the-art cGMP facility in Shirley, New York.
Our manufacturing facility is conveniently located in Shirley, New York, a short drive from either JFK or La Guardia airports.
Our manufacturing facility is conveniently located in Shirley, New York, a short drive from either JFK or La Guardia airports.

APL-Contract Development and Manufacturing Services

Contract drug development and contract manufacturing, including prototype formulation for APIs, excipients and packaging are performed with APL's most valuable resource - our competence and eagerness in fulfilling clients' needs.
Contract drug development and contract manufacturing, including prototype formulation for APIs, excipients and packaging are performed with APL's most valuable resource - our competence and eagerness in fulfilling clients' needs.
Our analytical chemists handle both chemicophysical quality control of drug substances and quality control of finished products. They can take care of your needs for method development and validation. We also conduct single stability studies in accordance with ICH guidelines.
Our analytical chemists handle both chemicophysical quality control of drug substances and quality control of finished products. They can take care of your needs for method development and validation. We also conduct single stability studies in accordance with ICH guidelines.
Our contract development and manufacturing services, in close relationship with patients and healthcare providers adds another dimension to our service.
Our contract development and manufacturing services, in close relationship with patients and healthcare providers adds another dimension to our service.
Sterile ointment manufacturing in our facility for sterile / aseptic manufacturing in Umeå.
Sterile ointment manufacturing in our facility for sterile / aseptic manufacturing in Umeå.
Glass vial filling services are part of APL's range of  pharmaceutical procurement services.
Glass vial filling services are part of APL's range of pharmaceutical procurement services.

Avantium Technologies-High Throughput Experimentation

X-ray powder diffraction.
X-ray powder diffraction.
Single crystal XRD.
Single crystal XRD.
Solid form characterization.
Solid form characterization.
Well plate crystallization.
Well plate crystallization.
High-throughput solubility testing.
High-throughput solubility testing.

B Braun OEM-Pharmaceutical Outsourcing Solutions, Contract Manufacturing and Project Management

B. Braun OEM offers a wide range of products and services for the pharmaceutical and medical device industry.
B. Braun OEM offers a wide range of products and services for the pharmaceutical and medical device industry.
Over 40 production sites and offices worldwide all adhere to international quality standards.
Over 40 production sites and offices worldwide all adhere to international quality standards.
Partnering with OEM offers innovative technologies, including system components and different container types.
Partnering with OEM offers innovative technologies, including system components and different container types.

Baxter Healthcare Corporation's BioPharma Solutions Business-Full Contract Service Capabilities

We offer high-speed capacity for large-scale syringe filling, aseptic formulation, vial filling, advanced lyophilization, and more in our versatile Bloomington, Indiana facility (recognized as a Facility of the Year in 2006).
We offer high-speed capacity for large-scale syringe filling, aseptic formulation, vial filling, advanced lyophilization, and more in our versatile Bloomington, Indiana facility (recognized as a Facility of the Year in 2006).
Baxter’s investment in advanced biologic capabilities helps you manufacture your complex molecule successfully and efficiently - without costly investment in specialized facilities, technology, and people.
Baxter’s investment in advanced biologic capabilities helps you manufacture your complex molecule successfully and efficiently - without costly investment in specialized facilities, technology, and people.
Our cytotoxic manufacturing capabilities include lyophilization, aseptic liquid fill of vials, dry powder vial filling, sterile crystallization and more.
Our cytotoxic manufacturing capabilities include lyophilization, aseptic liquid fill of vials, dry powder vial filling, sterile crystallization and more.
Baxter has over 15 years of experience in developing and manufacturing monoclonal antibodies and recombinant proteins.
Baxter has over 15 years of experience in developing and manufacturing monoclonal antibodies and recombinant proteins.

Boehringer Ingelheim Mexico-Production of Solid and Liquid Dosage Forms

Our industrial complex in Mexico has a production capacity of 140 million units per year.
Our industrial complex in Mexico has a production capacity of 140 million units per year.
Our plant includes an aluminum / PVC blister line (Marchesini, Gamma / Uhlmann), a bottled solid forms line (Kalish) and an aluminum / paper blister lines (IMA).
Our plant includes an aluminum / PVC blister line (Marchesini, Gamma / Uhlmann), a bottled solid forms line (Kalish) and an aluminum / paper blister lines (IMA).
We have a production plant dedicated to solid dosage forms that is equipped with state-of-the-art technology.
We have a production plant dedicated to solid dosage forms that is equipped with state-of-the-art technology.
Our production systems eliminate the risk of contamination while simultaneously optimizing both time and movement.
Our production systems eliminate the risk of contamination while simultaneously optimizing both time and movement.
Boehringer Ingelheim offers modern facilities for the storage of finished pharmaceutical goods.
Boehringer Ingelheim offers modern facilities for the storage of finished pharmaceutical goods.

Cangene-cGMP manufacturing service, Microbial Fermentation, Aseptic Fill / Finish and Aseptic Equipment

Cangene offers full service biopharmaceutical contract manufacturing capabilities including microbial fermentation, plasma fractionation, protein purification, aseptic filling, labeling, packaging and QC testing.
Cangene offers full service biopharmaceutical contract manufacturing capabilities including microbial fermentation, plasma fractionation, protein purification, aseptic filling, labeling, packaging and QC testing.
Cangene's 61,000ft² biopharmaceutical facility is designed for the manufacture of recombinant proteins up to 2,100L working volume.
Cangene's 61,000ft² biopharmaceutical facility is designed for the manufacture of recombinant proteins up to 2,100L working volume.
Chesapeake Biological Labs (CBL), established in 1980 and now a subsidiary of Cangene, is a recognized leader in the development and production of sterile biopharmaceuticals.
Chesapeake Biological Labs (CBL), established in 1980 and now a subsidiary of Cangene, is a recognized leader in the development and production of sterile biopharmaceuticals.
Cangene is a fully integrated biopharmaceutical company that provides a wide range of development and cGMP manufacturing services.
Cangene is a fully integrated biopharmaceutical company that provides a wide range of development and cGMP manufacturing services.
Aseptic fill / finish manufacturing experience includes recombinant proteins, plasma-derived proteins, plasmid DNA, liposomes and oligonucleotides. These products are manufactured in full compliance with cGMP in our FDA-licensed facility.
Aseptic fill / finish manufacturing experience includes recombinant proteins, plasma-derived proteins, plasmid DNA, liposomes and oligonucleotides. These products are manufactured in full compliance with cGMP in our FDA-licensed facility.

Catalent Pharma Solutions-Pharmaceutical Development, Drug Delivery, Manufacturing and Packaging

Catalent manufactures a wide range of sterile products utilizing blow / fill / seal.
Catalent manufactures a wide range of sterile products utilizing blow / fill / seal.
Complete lyophilization services from development to commercial product.
Complete lyophilization services from development to commercial product.
The Zydis® fast-dissolving dosage form dissolves instantly on the tongue and does not require water to aid swallowing.
The Zydis® fast-dissolving dosage form dissolves instantly on the tongue and does not require water to aid swallowing.
We are the world's leader in softgel manufacturing.
We are the world's leader in softgel manufacturing.
We offer a full range of trade and sample packaging services, printed components, promotional printing, clinical trials packaging and anti-counterfeiting technologies to protect your brand.
We offer a full range of trade and sample packaging services, printed components, promotional printing, clinical trials packaging and anti-counterfeiting technologies to protect your brand.

Cenexi-Contract Manufacturer for Injectable Ampoules, Tablets, Hard Gelatine Capsules, Syrups, Suppositories and Packaging for Prescriptions

Cenexi opened up its facilities to other pharmaceutical players, including customers supplying own-label products, while continuing to make products for its parent company, Roche Group.
Cenexi opened up its facilities to other pharmaceutical players, including customers supplying own-label products, while continuing to make products for its parent company, Roche Group.
Cenexi is offering a range of outsourcing services including analytical development, stability studies and assistance for product technical registration.
Cenexi is offering a range of outsourcing services including analytical development, stability studies and assistance for product technical registration.
Cenexi produces injectable ampoules and has probably one of the highest capacities in Europe (200 million ampoules for parenterals), bringing this galenical product into a high volume and low costs logical process.
Cenexi produces injectable ampoules and has probably one of the highest capacities in Europe (200 million ampoules for parenterals), bringing this galenical product into a high volume and low costs logical process.
Production of solid form for dry, wet and alcoholic granulation.
Production of solid form for dry, wet and alcoholic granulation.
Packaging drawing at your design.
Packaging drawing at your design.

Chanelle Medical-Pharmaceutical Contract Manufacturing and Packaging, and Generic Product Development

Chanelle Medical offers contract manufacturing and contracting packaging of tablets, capsules, liquids, powders and sachets.
Chanelle Medical offers contract manufacturing and contracting packaging of tablets, capsules, liquids, powders and sachets.
Chanelle Medical is an Irish based company, privately owned by Michael Burke, with 240 employees and a turnover of €42 million in 2006.
Chanelle Medical is an Irish based company, privately owned by Michael Burke, with 240 employees and a turnover of €42 million in 2006.
Chanelle Medical offers a service of analysing bulk that is manufactured outside the EU and releasing it for packing.
Chanelle Medical offers a service of analysing bulk that is manufactured outside the EU and releasing it for packing.

Christison Particle Technologies-Particle Characterisation Services

Our clean room facilities are available for cGMP micronising and cGMP microfluidising.
Our clean room facilities are available for cGMP micronising and cGMP microfluidising.
The Microjet laboratory processor offers particle size reduction and process control capabilities that are second to none.<
The Microjet laboratory processor offers particle size reduction and process control capabilities that are second to none.<
The Camsizer sets a new standard for the analysis of dry, pourable bulk materials.
The Camsizer sets a new standard for the analysis of dry, pourable bulk materials.
The DPA4100 particle analyzer has been shown to be superior for the detection, enumeration and characterisation of particles.
The DPA4100 particle analyzer has been shown to be superior for the detection, enumeration and characterisation of particles.
Christison offer various sieve shakers and sieve machines including the Rhewum precision air-jet sieve.
Christison offer various sieve shakers and sieve machines including the Rhewum precision air-jet sieve.

Cooper Maroc-Pharmaceutical Drug Production, Out-Licensing and In-Licensing

Cooper Maroc's four main strategic pharmaceutical businesses are distribution activity, branded generics activity, export and out-licensing, and in-licensing.
Cooper Maroc's four main strategic pharmaceutical businesses are distribution activity, branded generics activity, export and out-licensing, and in-licensing.
We manufacture capsules, syrups, tablets, sterile injections and ointments.
We manufacture capsules, syrups, tablets, sterile injections and ointments.
Cooper Maroc has built strong pharmaceutical brands in competitive therapeutic areas.
Cooper Maroc has built strong pharmaceutical brands in competitive therapeutic areas.
Cooper Maroc focuses on the pharmaceutical export market.
Cooper Maroc focuses on the pharmaceutical export market.
Cooper Maroc builds its in-licensing activities on successful partnerships in sales, marketing, 'toll manufacturing' and licence agreements with other pharmaceutical companies.
Cooper Maroc builds its in-licensing activities on successful partnerships in sales, marketing, 'toll manufacturing' and licence agreements with other pharmaceutical companies.

Covidien Pharmaceuticals Outsourcing -Pharmaceutical Contract Manufacturer Focusing on Solid and Oral Liquid Dosage Forms

The finished product manufacturing facility in Hobart, NY is FDA and DEA I-V compliant and is operated under cGMP conditions.
The finished product manufacturing facility in Hobart, NY is FDA and DEA I-V compliant and is operated under cGMP conditions.
Covidien has added over  350 ,000ft² of manufacturing and packaging suites to the Hobart, New York site.
Covidien has added over 350 ,000ft² of manufacturing and packaging suites to the Hobart, New York site.
Covidien has invested over $150 million in the Hobart facility since 1996, including oral non-sterile liquid production, high-speed encapsulation and tablet presses.
Covidien has invested over $150 million in the Hobart facility since 1996, including oral non-sterile liquid production, high-speed encapsulation and tablet presses.
New packaging capabilities include unit dose with bar coded blister packs.
New packaging capabilities include unit dose with bar coded blister packs.
Facilities undergo regular audits by both regulatory agencies and clients to ensure that quality standards are met and exceeded.
Facilities undergo regular audits by both regulatory agencies and clients to ensure that quality standards are met and exceeded.

Dragenopharm-Contract Manufacturing of Sugar Coated Tablets, Film Coated Tablets and Hard Gelatine Capsules

Dragenopharm's contract manufacturing plant includes tablet pressing rooms for manufacturing laminated tablets and multi-layer tablets.
Dragenopharm's contract manufacturing plant includes tablet pressing rooms for manufacturing laminated tablets and multi-layer tablets.
Dragenopharm's tablets are film coated in an explosion-proof film coating room.
Dragenopharm's tablets are film coated in an explosion-proof film coating room.
The tablet sugar coating area of our contract manufacturing plant contains 40 Brucks coating pans of 250kg capacity.
The tablet sugar coating area of our contract manufacturing plant contains 40 Brucks coating pans of 250kg capacity.
Dragenopharm's laboratory is used for analysis of both the raw materials used in the production of tablets and capsules, and the final product.
Dragenopharm's laboratory is used for analysis of both the raw materials used in the production of tablets and capsules, and the final product.
Dragenopharm provides tablet and capsule packaging and bottling services.
Dragenopharm provides tablet and capsule packaging and bottling services.

EMS-Generic and Prescription Pharmaceuticals

EMS is renowned as a leading supplier of value-added prescription drugs, and the largest line of generic drugs in Brazil.
EMS is renowned as a leading supplier of value-added prescription drugs, and the largest line of generic drugs in Brazil.
EMS produces liquid, solid, semi-solid, injectable and soft-gel caps. We have expertise across a wide range of prescription medicine, generics, hospital and OTC sectors and applications.
EMS produces liquid, solid, semi-solid, injectable and soft-gel caps. We have expertise across a wide range of prescription medicine, generics, hospital and OTC sectors and applications.
Our reputation as a manufacturer of high quality cyclosporine microemulsion is a source of pride to the whole Group.
Our reputation as a manufacturer of high quality cyclosporine microemulsion is a source of pride to the whole Group.
Germed, a European affiliate of EMS, markets generic and prescription pharmaceutical products in Portugal. EMS is EU GMP approved to export solid, semi-solid forms, soft-gel caps, liquids and creams to Europe.
Germed, a European affiliate of EMS, markets generic and prescription pharmaceutical products in Portugal. EMS is EU GMP approved to export solid, semi-solid forms, soft-gel caps, liquids and creams to Europe.
EMS is the first laboratory to get approval from Anvisa (Brazil's national health vigilance agency) to produce generic drugs in Brazil.
EMS is the first laboratory to get approval from Anvisa (Brazil's national health vigilance agency) to produce generic drugs in Brazil.

Ferro Pfanstiehl Laboratories-API Chemical Process Development and Manufacturing

Ferro Pfanstiehl Laboratories' Safebridge-certified high potency active pharmaceutical ingredient 1200gal multi-purpose reactor suite.
Ferro Pfanstiehl Laboratories' Safebridge-certified high potency active pharmaceutical ingredient 1200gal multi-purpose reactor suite.
FPL's Carlisle class IV full containment isolator is used for small-scale HPAPI finishing.
FPL's Carlisle class IV full containment isolator is used for small-scale HPAPI finishing.
Our ICH-Q7A-compliant analytical services laboratory is enabled CGMP product release testing and API stability testing.
Our ICH-Q7A-compliant analytical services laboratory is enabled CGMP product release testing and API stability testing.
The company produces large quantities of High Purity Low Endotoxin Carbohydrates servicing the biotechnology industry.
The company produces large quantities of High Purity Low Endotoxin Carbohydrates servicing the biotechnology industry.
FPL's ICH-Q7A-compliant quality assurance platform ensures a high standard of drug master file preparation and maintenance service provision.
FPL's ICH-Q7A-compliant quality assurance platform ensures a high standard of drug master file preparation and maintenance service provision.

FINE FOODS NTM SpA-Pharmaceutical and Nutraceutical Contract Manufacturing

FINE FOODS NTM is an independent contract manufacturer working in the field of pharmaceuticals and food supplements.
FINE FOODS NTM is an independent contract manufacturer working in the field of pharmaceuticals and food supplements.
FINE FOODS NTM is able to provide customers with stability tests, process validations, analytical methodologies development and validation.
FINE FOODS NTM is able to provide customers with stability tests, process validations, analytical methodologies development and validation.
FINE FOODS NTM has two production plants, one for pharmaceuticals, the second for food supplements.
FINE FOODS NTM has two production plants, one for pharmaceuticals, the second for food supplements.
FINE FOODS NTM produces all kinds of solid oral forms as well as many packaging forms.
FINE FOODS NTM produces all kinds of solid oral forms as well as many packaging forms.
The company also specialises in fluid bed granulation technology for effervescent products.
The company also specialises in fluid bed granulation technology for effervescent products.

Fresenius Product Partnering-Contract Development and Manufacture of Sterile Fluids

Fresenius have more than 18 manufacturing facilities worldwide.
Fresenius have more than 18 manufacturing facilities worldwide.
Fresenius has the flexibility to incorporate clients’ specific demands on container configuration, and has the expertise to advise on the possibilities of delivery systems.
Fresenius has the flexibility to incorporate clients’ specific demands on container configuration, and has the expertise to advise on the possibilities of delivery systems.
Fresenius manufacturing capabilities span the fill/finish of small and large volume sterile fluid solutions and emulsions. These are processed aseptically or terminally sterilized.
Fresenius manufacturing capabilities span the fill/finish of small and large volume sterile fluid solutions and emulsions. These are processed aseptically or terminally sterilized.
Fresenius provides full quality control support for starting materials, finished sterile products and all stages in between. This support includes physical, chemical and microbiological quality.
Fresenius provides full quality control support for starting materials, finished sterile products and all stages in between. This support includes physical, chemical and microbiological quality.

GP Grenzach Produktions GmbH-Manufacture, Packaging and Distribution of Pharmaceutical Products

As the manufacturer of Bepanthen® and Bepanthol®, we have extensive experience of working with ointments, creams, lotions and gels.
As the manufacturer of Bepanthen® and Bepanthol®, we have extensive experience of working with ointments, creams, lotions and gels.
Grenzach can, under aseptic conditions, fill syringes or vials with sterile-filtered bulk products.
Grenzach can, under aseptic conditions, fill syringes or vials with sterile-filtered bulk products.
Our strength lies not just in our ability to carry out small packaging orders rapidly and efficiently - special tasks like the charging of displays and the addition of measuring cups, beakers and other application aids are also our speciality.
Our strength lies not just in our ability to carry out small packaging orders rapidly and efficiently - special tasks like the charging of displays and the addition of measuring cups, beakers and other application aids are also our speciality.
Tablets, coated tablets and capsules are packaged in PVC / PP or aluminium blisters and multi-dose glass or plastic containers with fitting secondary packaging.
Tablets, coated tablets and capsules are packaged in PVC / PP or aluminium blisters and multi-dose glass or plastic containers with fitting secondary packaging.
We carry out chemical-physical, microbiological and technical tests, as well as stability tests, on all the products we use or manufacture.
We carry out chemical-physical, microbiological and technical tests, as well as stability tests, on all the products we use or manufacture.

GP Pharm-Urology / Oncology Contract Manufacturing Services and Pharmaceutical Platforms

Our facility at Sant Quintí de Mediona Barcelona specialises in the manufacture of cytotoxic materials and high potency APIs, including depot and liposomal formulations.
Our facility at Sant Quintí de Mediona Barcelona specialises in the manufacture of cytotoxic materials and high potency APIs, including depot and liposomal formulations.
GP Pharm offers highly-skilled contract manufacturing services and proprietary pharmaceutical products in the fields of urology and oncology.
GP Pharm offers highly-skilled contract manufacturing services and proprietary pharmaceutical products in the fields of urology and oncology.
GP Pharm's developments in biodegradable polymers and liposomal formulations offer improved delivery profiles for cytotoxic and high potent APIs.
GP Pharm's developments in biodegradable polymers and liposomal formulations offer improved delivery profiles for cytotoxic and high potent APIs.

Groupe Novasep-Syntheses and Processes to Produce Molecules

Novasep Process is devoted to offering purification solutions to the life science industries and other markets.
Novasep Process is devoted to offering purification solutions to the life science industries and other markets.
Novasep's work meets all the international quality standards like cGMP, ISO, FDA.
Novasep's work meets all the international quality standards like cGMP, ISO, FDA.
Novasep's development team involves PhD chemists and biochemists for the analysis of the purification problem and development studies.
Novasep's development team involves PhD chemists and biochemists for the analysis of the purification problem and development studies.
Novasep Synthesis comprehensively covers the special needs of the pharmaceutical, food, cosmetics, agrochemicals, and specialty chemicals industries.
Novasep Synthesis comprehensively covers the special needs of the pharmaceutical, food, cosmetics, agrochemicals, and specialty chemicals industries.

Hasco-Lek-Contract Manufacturer and Service Provider for the Pharmaceutical and Nutraceutical Industry

Hasco-Lek is a producer of more than 200 pharmaceutical products. It also acts as a contract manufacturer and service provider for pharmaceutical and nutraceutical industry.
Hasco-Lek is a producer of more than 200 pharmaceutical products. It also acts as a contract manufacturer and service provider for pharmaceutical and nutraceutical industry.
The company has modern, cGMP approved production line as well as a research and development laboratory.
The company has modern, cGMP approved production line as well as a research and development laboratory.
Nutraceuticals, food supplements, dietary supplement products.
Nutraceuticals, food supplements, dietary supplement products.
Manufacturing pharmaceutical products in the form of softgels, tablets, syrups, liquids, ointments, gels, creams, powders and suppositories.
Manufacturing pharmaceutical products in the form of softgels, tablets, syrups, liquids, ointments, gels, creams, powders and suppositories.
The company also provides contract research services including formulation development, technology transfer, scale up, clinical trials and registration services.
The company also provides contract research services including formulation development, technology transfer, scale up, clinical trials and registration services.

Haupt Pharma-Drug Development, Clinical Trial Supplies and Contract Manufacturing

A wide variety of solid dosage forms are produced at Haupt Pharma, Berlin.
A wide variety of solid dosage forms are produced at Haupt Pharma, Berlin.
Haupt Pharma Brackenheim's clean room zones for the sealing of open products in blister packs.
Haupt Pharma Brackenheim's clean room zones for the sealing of open products in blister packs.
Ampoule filling is a speciality at Haupt Pharma Livron.
Ampoule filling is a speciality at Haupt Pharma Livron.
Haupt Pharma Münster’s area of expertise is the production of high-potent, low-dose drugs.
Haupt Pharma Münster’s area of expertise is the production of high-potent, low-dose drugs.
Isolator technology at Haupt Pharma Wolfratshausen’s sterile department.
Isolator technology at Haupt Pharma Wolfratshausen’s sterile department.

Health Protection Agency-Healthcare Product Research, Development and GMP Manufacture

The Health Protection Agency provides contract research, development and manufacture of healthcare products.
The Health Protection Agency provides contract research, development and manufacture of healthcare products.
The provision of a quality serological analytical service for the measurement of immune responses.
The provision of a quality serological analytical service for the measurement of immune responses.
Contract filling for biological products.
Contract filling for biological products.
GMP production plant featuring bacterial fermentation vessels.
GMP production plant featuring bacterial fermentation vessels.
The Health Protection Agency provides contract research for healthcare products including vaccines, enzymes, therapeutic proteins and other biologically derived compounds.
The Health Protection Agency provides contract research for healthcare products including vaccines, enzymes, therapeutic proteins and other biologically derived compounds.

Hetero Drugs-Active Pharmaceutical Ingredients (API), Generic Finished Dosages, Custom Synthesis And Contract Research

Hetero Drugs is one of the largest manufacturers of active pharmaceutical ingredients and finished dosages in the world.
Hetero Drugs is one of the largest manufacturers of active pharmaceutical ingredients and finished dosages in the world.
Of the nine active pharmaceutical ingredients manufacturing facilities of Hetero Drugs, four active pharmaceutical ingredients plants have been approved by the USFDA.
Of the nine active pharmaceutical ingredients manufacturing facilities of Hetero Drugs, four active pharmaceutical ingredients plants have been approved by the USFDA.
The WHO, Geneva, and several other international regulatory authorities have approved Hetero Drugs' facility for finished dosages.
The WHO, Geneva, and several other international regulatory authorities have approved Hetero Drugs' facility for finished dosages.
Hetero Drugs has established world-class facilities for custom synthesis and contract research to develop new chemical entities.
Hetero Drugs has established world-class facilities for custom synthesis and contract research to develop new chemical entities.
Hetero Drugs has a world-class research centre with 40 laboratories and 150 scientists and the company is well positioned to explore the opportunities in the custom synthesis, active pharmaceutical ingredients, finished dosages and contract research segments.
Hetero Drugs has a world-class research centre with 40 laboratories and 150 scientists and the company is well positioned to explore the opportunities in the custom synthesis, active pharmaceutical ingredients, finished dosages and contract research segments.

IDT Biologika-Contract Manufacturing and Development of Vaccines and Pharmaceuticals

IDT has specific competences in filling and packaging of syringes.
IDT has specific competences in filling and packaging of syringes.
IDT provides a wide range of contract development services such as development and optimisation of lyophilisation processes.
IDT provides a wide range of contract development services such as development and optimisation of lyophilisation processes.
The production complex for pharmaceutical contract manufacturing has a high technological standard and is successfully inspected by national and international authorities.
The production complex for pharmaceutical contract manufacturing has a high technological standard and is successfully inspected by national and international authorities.
Innovative solutions, extensive experience and the use of latest technologies make IDT a well-recognised contract manufacturer for vaccines.
Innovative solutions, extensive experience and the use of latest technologies make IDT a well-recognised contract manufacturer for vaccines.
Viral and bacterial vaccines are manufactured and developed for third parties by IDT.
Viral and bacterial vaccines are manufactured and developed for third parties by IDT.

LaborMed Pharma-Cardiovascular Medicines

LaborMed Pharma is one of the largest independent generic companies in Romania and a top supplier of cardiovascular medicines for the domestic market.
LaborMed Pharma is one of the largest independent generic companies in Romania and a top supplier of cardiovascular medicines for the domestic market.
LaborMed's new plant boasts state-of-the-art technologies and the highest quality standards.
LaborMed's new plant boasts state-of-the-art technologies and the highest quality standards.
All units related to the manufacturing process (production, storage, analytic lab, microbiologic lab, the energetic block and the administrative area) are networked ensuring detailed monitoring of every stage of the process.
All units related to the manufacturing process (production, storage, analytic lab, microbiologic lab, the energetic block and the administrative area) are networked ensuring detailed monitoring of every stage of the process.
LaborMed Pharma's first-to-market strategy is supported by strong R&D and regulatory capabilities.
LaborMed Pharma's first-to-market strategy is supported by strong R&D and regulatory capabilities.

Laureate Pharma-Biopharmaceutical Development and Production

Laureate Pharma provides superior bioprocessing services that accelerate new products from development through production.
Laureate Pharma provides superior bioprocessing services that accelerate new products from development through production.
Laureate Pharma offers aseptic fill and finish services to formulate and fill the final product.
Laureate Pharma offers aseptic fill and finish services to formulate and fill the final product.
Laureate Pharma’s labs are registered with the US Food and Drug Administration (FDA) and licensed by the Drug Enforcement Administration (DEA) and the Nuclear Regulatory Commission.
Laureate Pharma’s labs are registered with the US Food and Drug Administration (FDA) and licensed by the Drug Enforcement Administration (DEA) and the Nuclear Regulatory Commission.

LOBA Feinchemie-Active Pharmaceutical Ingredients (API), Intermediates, Reagents, Diagnostics, Custom Synthesis and Process Development

One of the reaction vessels with glassware for production of APIs.
One of the reaction vessels with glassware for production of APIs.
Silicon carbide heat exchangers offer substantial advantage compared with glass or graphite.
Silicon carbide heat exchangers offer substantial advantage compared with glass or graphite.
A peeler centrifuge is used to isolate the products, it is CIP equipped.
A peeler centrifuge is used to isolate the products, it is CIP equipped.
Vacuum drying oven in the clean room area - 18m², 8mbar, max 120°C.
Vacuum drying oven in the clean room area - 18m², 8mbar, max 120°C.
Entrance airlocks to the clean room area including pressure indicators and entrance control system.
Entrance airlocks to the clean room area including pressure indicators and entrance control system.

Lomapharm®-Contract Manufacturing of Mineral Based Drugs and Nutrition Supplements

Our analytical laboratories.
Our analytical laboratories.
Blistering line production.
Blistering line production.
Our filling lines are designed for filling operations under aseptic and sterile conditions.
Our filling lines are designed for filling operations under aseptic and sterile conditions.
Unique expertise in sugar coating of tablets.
Unique expertise in sugar coating of tablets.
Our compression machines eject up to 250,000 tablets per hour with a total capacity of more than 1 billion tablets.
Our compression machines eject up to 250,000 tablets per hour with a total capacity of more than 1 billion tablets.

Lonza-Custom Pharmaceutical and Biotechnological Manufacturing Solutions

Our most important asset is our highly qualified personnel and their extensive expertise in responsive, process-oriented project management.
Our most important asset is our highly qualified personnel and their extensive expertise in responsive, process-oriented project management.
We offer a full range of research and services, from cell line development and process optimisation, to regulatory assistance and technology transfer support.
We offer a full range of research and services, from cell line development and process optimisation, to regulatory assistance and technology transfer support.
Our state-of-the art cGMP facilities will help you maximise every opportunity to gain an advantage in your race to market.
Our state-of-the art cGMP facilities will help you maximise every opportunity to gain an advantage in your race to market.
Lonza has developed a highly efficient mammalian expression and vector amplification system that makes use of selection via glutamine metabolism and powerful viral promoters. [© Martin Oeggerli]
Lonza has developed a highly efficient mammalian expression and vector amplification system that makes use of selection via glutamine metabolism and powerful viral promoters. [© Martin Oeggerli]
Lonza is building Asia's most advanced mammalian cell culture manufacturing facility, in Tuas Biomedical Park, Singapore.
Lonza is building Asia's most advanced mammalian cell culture manufacturing facility, in Tuas Biomedical Park, Singapore.

Luxembourg Industries-Speciality Chemicals and Fine Chemicals for the Biotechnology and Pharmaceutical Industries

Luxembourg Industries is a leading manufacturer and supplier of specialty and fine chemicals. The company develops, sources, produces and supplies high quality and safe products, designed to fit customers’ requirements (including GMP).
Luxembourg Industries is a leading manufacturer and supplier of specialty and fine chemicals. The company develops, sources, produces and supplies high quality and safe products, designed to fit customers’ requirements (including GMP).
Luxembourg Industries' two processing plants in Israel production is done on a wide scale from gram to multi-ton lots of specialty and fine chemicals for biotechnology and pharmaceutical industry applications.
Luxembourg Industries' two processing plants in Israel production is done on a wide scale from gram to multi-ton lots of specialty and fine chemicals for biotechnology and pharmaceutical industry applications.
Luxembourg Industries production units are multi-scale combined with a variety of process equipments and in house process development. The production is focused on the industry and the researcher requirements.
Luxembourg Industries production units are multi-scale combined with a variety of process equipments and in house process development. The production is focused on the industry and the researcher requirements.
Luxembourg Industries' independent state-of-the-art research, development and production facilities, located at their main manufacturing sites, provide early access to desired new molecules, on-site production services, and short time from development to production.
Luxembourg Industries' independent state-of-the-art research, development and production facilities, located at their main manufacturing sites, provide early access to desired new molecules, on-site production services, and short time from development to production.

MEDA Manufacturing-Solid, Semi-Solid and Liquid Dosage Forms

As a future-oriented pharmaceutical company, MEDA Manufacturing has many years' experience in manufacturing solid, semi-solid and liquid dosage forms.
As a future-oriented pharmaceutical company, MEDA Manufacturing has many years' experience in manufacturing solid, semi-solid and liquid dosage forms.
MEDA Manufacturing manufactures virtually all dosage forms as well as a variety of speciality products.
MEDA Manufacturing manufactures virtually all dosage forms as well as a variety of speciality products.
MEDA Manufacturing supervises your projects from product development and pilot production, through scale-up, cleaning and process validation, to commercial production.
MEDA Manufacturing supervises your projects from product development and pilot production, through scale-up, cleaning and process validation, to commercial production.
We use the latest equipment and technologies, such as HPLC, GC, FTIR, UV spectroscopy and NIR to conduct analyses on everything from incoming raw materials to finished products.
We use the latest equipment and technologies, such as HPLC, GC, FTIR, UV spectroscopy and NIR to conduct analyses on everything from incoming raw materials to finished products.
MEDA Manufacturing has successfully been manufacturing pharmaceutical products that meet the highest quality standards for pharmaceutical companies in Germany and abroad for years.
MEDA Manufacturing has successfully been manufacturing pharmaceutical products that meet the highest quality standards for pharmaceutical companies in Germany and abroad for years.

Micron Technologies-Global, cGMP Micronizing and Milling for the Pharmaceutical Industry

Micron Technologies offers a truly international, state-of-the-art cGMP particle size reduction service dedicated to serving the needs of the global pharmaceutical industry.
Micron Technologies offers a truly international, state-of-the-art cGMP particle size reduction service dedicated to serving the needs of the global pharmaceutical industry.
We own two directly compatible facilities, one based in the UK and the other in the USA.
We own two directly compatible facilities, one based in the UK and the other in the USA.
At Micron Technologies we are dedicated to the efficient processing of customers' materials, ensuring the maintenance of the highest quality standards.
At Micron Technologies we are dedicated to the efficient processing of customers' materials, ensuring the maintenance of the highest quality standards.
We carry out a broad range of analytical services, including polymorph and amorphous information.
We carry out a broad range of analytical services, including polymorph and amorphous information.
We believe in maintaining the highest standards of Good Manufacturing Practice and complying with the current requirements of the regulatory authorities.
We believe in maintaining the highest standards of Good Manufacturing Practice and complying with the current requirements of the regulatory authorities.

NextPharma-Product Development, Contract Manufacturing and Distribution

NextPharma have a breadth of capabilities in development, manufacture and distribution of pharmaceuticals.
NextPharma have a breadth of capabilities in development, manufacture and distribution of pharmaceuticals.
We support our customers from drug development to packaging.
We support our customers from drug development to packaging.
Our customers include many of the world’s leading pharmaceutical companies.
Our customers include many of the world’s leading pharmaceutical companies.
Each project manager is responsible for managing projects from inception to completion.
Each project manager is responsible for managing projects from inception to completion.

Nycomed-Global Contract Services for Pharmaceutical Production

Nycomed provides a range of technologies for the production and packaging of solid and liquid pharmaceuticals.
Nycomed provides a range of technologies for the production and packaging of solid and liquid pharmaceuticals.
After its recent acquisition of ALTANA Pharma, Nycomed is adding to its global pharmaceutical contract manufacturing activities.
After its recent acquisition of ALTANA Pharma, Nycomed is adding to its global pharmaceutical contract manufacturing activities.
Nycomed gives access to its long lasting pharma expertise and capacities in Active Pharmaceutical Ingredient (API) manufacture.
Nycomed gives access to its long lasting pharma expertise and capacities in Active Pharmaceutical Ingredient (API) manufacture.

Onyx Scientific-Lead Optimisation, Process Development and Scale-Up Synthesis

If you are sourcing a partner for lead optimisation, process development and scale-up synthesis, or just want excellent chemistry support, Onyx Scientific provides a partnership of the highest standard.
If you are sourcing a partner for lead optimisation, process development and scale-up synthesis, or just want excellent chemistry support, Onyx Scientific provides a partnership of the highest standard.
Onyx Scientific provides a value-added service with an emphasis on compound quality, purity and pharmacological properties.
Onyx Scientific provides a value-added service with an emphasis on compound quality, purity and pharmacological properties.
Our facilities enable Onyx to provide a comprehensive service in process research and development, and API production for phase I and II clinical trials.
Our facilities enable Onyx to provide a comprehensive service in process research and development, and API production for phase I and II clinical trials.

Organon-Pharmaceutical and Biopharmaceutical Drugs and Ingredients

Organon is an ideal partner in pharmaceutical manufacturing and development services, offering exceptional technical capabilities, experience and infrastructure.
Organon is an ideal partner in pharmaceutical manufacturing and development services, offering exceptional technical capabilities, experience and infrastructure.
Organon's drug-product services include tabletting, caps, suppositories, ampoules (solution and lyophilized), vials (solution and lyophilized), bottles, syringes, creams, implants moulding, implants filling in ampoules, and implants filling in vials.
Organon's drug-product services include tabletting, caps, suppositories, ampoules (solution and lyophilized), vials (solution and lyophilized), bottles, syringes, creams, implants moulding, implants filling in ampoules, and implants filling in vials.
Organon's advanced facilities and highly-trained employees provide outstanding quality in studies, activities, processes and products, ensuring the successful development, registration and production of safe medicines.
Organon's advanced facilities and highly-trained employees provide outstanding quality in studies, activities, processes and products, ensuring the successful development, registration and production of safe medicines.
Organon offers a broad range of services, from formulation development, stability investigations, process development and analytical development, to qualification and scale-up, through manufacturing and packaging of products, to support clinical trials and commercial sale.
Organon offers a broad range of services, from formulation development, stability investigations, process development and analytical development, to qualification and scale-up, through manufacturing and packaging of products, to support clinical trials and commercial sale.

Pierre Fabre Medicament - Active Ingredients Division-Product Extraction and Purification - Cytotoxic API Manufacturing

Our production areas, based in France and Argentina, are equipped with continuous extraction lines (up to 1,000kg/h) and horizontal batch extractors.
Our production areas, based in France and Argentina, are equipped with continuous extraction lines (up to 1,000kg/h) and horizontal batch extractors.
We have developed a broad know-how in purification of complex mixtures to isolate pure single molecules.
We have developed a broad know-how in purification of complex mixtures to isolate pure single molecules.
This technology offers many advantages compared to standard methods: no solid phase, no irreversible adsorption, quantities of solvent dramatically decreased and pH-based purification.
This technology offers many advantages compared to standard methods: no solid phase, no irreversible adsorption, quantities of solvent dramatically decreased and pH-based purification.
We also offer our partners a technology to dramatically enhance bioavailability of APIs using SuperCritical CO2.
We also offer our partners a technology to dramatically enhance bioavailability of APIs using SuperCritical CO2.
Pierre Fabre Medicament has been ISO 14001 certified since 1998 and awarded by the French Ministry of Environment for our efforts within environment protection.
Pierre Fabre Medicament has been ISO 14001 certified since 1998 and awarded by the French Ministry of Environment for our efforts within environment protection.

Polymun Scientific-Biopharmaceutical and Liposomal Manufacturing and Contract Development

Your biopharmaceutical cell line is in good hands at Polymun.
Your biopharmaceutical cell line is in good hands at Polymun.
Our team is experienced in handling sophisticated processes.
Our team is experienced in handling sophisticated processes.
Polymun has a clear understanding of purification.
Polymun has a clear understanding of purification.
Comprehensive documentation is important to us.
Comprehensive documentation is important to us.
We care for your pharmaceutical product.
We care for your pharmaceutical product.

PolyPeptide Laboratories-Active Pharmaceutical Ingredient (API) Manufacturer, Custom and gmp peptides

Large-scale high-pressure liquid chromatography (HPLC) is a frequently used method of purification for peptides.
Large-scale high-pressure liquid chromatography (HPLC) is a frequently used method of purification for peptides.
Solid phase peptide synthesis (SPPS) in a 250l reactor.
Solid phase peptide synthesis (SPPS) in a 250l reactor.
In-process purification often requires a variety of chromatographic approaches.
In-process purification often requires a variety of chromatographic approaches.
Isolators in freeze drying facilities at PolyPeptide Laboratories.
Isolators in freeze drying facilities at PolyPeptide Laboratories.
Solution-phase manufacturing at PolyPeptide Laboratories.
Solution-phase manufacturing at PolyPeptide Laboratories.

Rentschler Pharma-Pharmaceutical Development Services, Contract Manufacturing and Packaging of Solid Pharmaceuticals and Food Supplements

Rentschler Pharma offers a great variety of different delivery systems for solid dosage forms.
Rentschler Pharma offers a great variety of different delivery systems for solid dosage forms.
Our development department works in close collaboration with our customers and gives advice on the choice of the appropriate technology.
Our development department works in close collaboration with our customers and gives advice on the choice of the appropriate technology.
Automatic banding of hard capsules using a Bonapace BD-3000 system.
Automatic banding of hard capsules using a Bonapace BD-3000 system.
Rentschler Pharma - full service contract manufacturer for solid dosage forms.
Rentschler Pharma - full service contract manufacturer for solid dosage forms.
At Rentschler Pharma, product quality is a must.
At Rentschler Pharma, product quality is a must.

Rottendorf Pharma-Manufacture and Development of Solid Dosage Forms

Rottendorf Pharma is one of Europe’s leading contract manufacturers for solid dosage forms.
Rottendorf Pharma is one of Europe’s leading contract manufacturers for solid dosage forms.
Founded as a family business in Berlin in 1928, Rottendorf Pharma has been situated in Ennigerloh since 1949.
Founded as a family business in Berlin in 1928, Rottendorf Pharma has been situated in Ennigerloh since 1949.
Being exclusively a contract manufacturer, Rottendorf Pharma is a customer-orientated and reliable partner for your solid dosage forms.
Being exclusively a contract manufacturer, Rottendorf Pharma is a customer-orientated and reliable partner for your solid dosage forms.
We carry out established routine analyses with the most advanced analytical equipment and according to the latest methods.
We carry out established routine analyses with the most advanced analytical equipment and according to the latest methods.
Our service range covers product development, galenical process development, analytical process development, production and packaging.
Our service range covers product development, galenical process development, analytical process development, production and packaging.

ROVI-Aseptic Filling of Small Volume Parenterals

Contract manufacturing facilities in Madrid, Spain.
Contract manufacturing facilities in Madrid, Spain.
Pre-filled syringes of 0.2ml to 5ml.
Pre-filled syringes of 0.2ml to 5ml.
Pre-filled vials of 2ml to 20ml.
Pre-filled vials of 2ml to 20ml.
Clean areas for aseptic filling.
Clean areas for aseptic filling.
Visual inspection system for pre-filled syringes and vials.
Visual inspection system for pre-filled syringes and vials.

State Pharmaceuticals Manufacturing Corporation-Pharmaceutical Production

The State Pharmaceuticals Manufacturing Corporation (SPMC) specialises in the manufacture of quality tablets, capsules and dry powders.
The State Pharmaceuticals Manufacturing Corporation (SPMC) specialises in the manufacture of quality tablets, capsules and dry powders.
SPMC products are well accepted and recognized by doctors, pharmacists and other professionals in the health sector.
SPMC products are well accepted and recognized by doctors, pharmacists and other professionals in the health sector.
SPMC is dedicated to the provision of safe and effective drugs at affordable prices to the national healthcare system and the general public.
SPMC is dedicated to the provision of safe and effective drugs at affordable prices to the national healthcare system and the general public.

Synprosis-Peptide, Protein and Synthetic Vaccine Developments

Synprosis is specialized in solid phase manufacture of peptides and synthetic small proteins for basic research and for therapeutic applications (cGMP)
Synprosis is specialized in solid phase manufacture of peptides and synthetic small proteins for basic research and for therapeutic applications (cGMP)
We are specializing in the manufacture of peptides and small proteins (120 AA) for basic research and for therapeutic applications.
We are specializing in the manufacture of peptides and small proteins (120 AA) for basic research and for therapeutic applications.
Synprosis is a French company specialized in synthetic vaccine developments.
Synprosis is a French company specialized in synthetic vaccine developments.

Temmler Pharma-Contract Manufacture, Contract Development and Regulatory Services

Encapsulation.
Encapsulation.
Blister packaging.
Blister packaging.
HPLC testing.
HPLC testing.
Tabletting.
Tabletting.
Fluid bed drying granulation.
Fluid bed drying granulation.

Unither-Blow, Fill and Seal Technology, Effervescent Tablets and Liquid Stick-Packs

Our sterile unit-dose vials are easy to use, preservative free and easy to carry. They are one of the most accurate ways to ensure that you deliver the right dose every time.
Our sterile unit-dose vials are easy to use, preservative free and easy to carry. They are one of the most accurate ways to ensure that you deliver the right dose every time.
Unither's effervescent tablets are easy to take and rapid-action.
Unither's effervescent tablets are easy to take and rapid-action.
Liquid stick-packs are easy to carry and use. The stick provides a barrier effect.
Liquid stick-packs are easy to carry and use. The stick provides a barrier effect.
As part of an industrial group, Unither can provide its clients with full-service project development - from formulation to industrial manufacture.
As part of an industrial group, Unither can provide its clients with full-service project development - from formulation to industrial manufacture.

Vetter-Aseptically Pre-Filled Application Systems

Patient-friendly, pre-filled application systems.
Patient-friendly, pre-filled application systems.
V-OVS NS(R) - the new closure system for pre-filled syringes.
V-OVS NS(R) - the new closure system for pre-filled syringes.
Vetter's new facility is category winner of the Facility of the Year Awards.
Vetter's new facility is category winner of the Facility of the Year Awards.
Vetter's new facility is category winner of the European Outsourcing Awards.
Vetter's new facility is category winner of the European Outsourcing Awards.

VINS Bioproducts-Snake Venom Antiserum, Rabies Antiserum and Anti-Sera Products

VINS Bioproducts offers snake venom antiserum, rabies antiserum, carboplatin, bleomycin, daunorubicin, ifosfamide and epirubicin medicines for domestic and global markets.
VINS Bioproducts offers snake venom antiserum, rabies antiserum, carboplatin, bleomycin, daunorubicin, ifosfamide and epirubicin medicines for domestic and global markets.
The snake venom antiserum is equine-based immunoglobulin enzyme treated.
The snake venom antiserum is equine-based immunoglobulin enzyme treated.
The snake venom antiserum is equine-based immunoglobulin enzyme treated.
The snake venom antiserum is equine-based immunoglobulin enzyme treated.
The rabies antiserum IP is presented as a liquid product with 300 IU in each vial.
The rabies antiserum IP is presented as a liquid product with 300 IU in each vial.
VIN Rab is the second product of the company and is available as a liquid product with 1,000 IU in each vial.
VIN Rab is the second product of the company and is available as a liquid product with 1,000 IU in each vial.

Wockhardt-Pharmaceutical Contract Manufacturing

Discover a contract manufacturer with more to offer.
Discover a contract manufacturer with more to offer.
Wockhardt has recently implemented a four-fold expansion in cartridge manufacturing capabilities.
Wockhardt has recently implemented a four-fold expansion in cartridge manufacturing capabilities.
Our solid dose facilities provide manufacturing and packing for both plain tablets and film or sugar coated tablets.
Our solid dose facilities provide manufacturing and packing for both plain tablets and film or sugar coated tablets.
Wockhardt's production capabilities now cover sachets, powders, liquids, ointments and creams.
Wockhardt's production capabilities now cover sachets, powders, liquids, ointments and creams.
Wockhardt's state-of-the-art sterile injectable facility offers the manufacture of high-potency products.
Wockhardt's state-of-the-art sterile injectable facility offers the manufacture of high-potency products.

Xenova Biomanufacturing-Biologics Contract Development and Manufacture

Xenovabio delivers quality vaccines, therapeutic proteins and viral vectors for phase I, II and III clinical trials.
Xenovabio delivers quality vaccines, therapeutic proteins and viral vectors for phase I, II and III clinical trials.
We provide reliable manufacture of a wide range of candidate biologics in GMP-compliant facilities.
We provide reliable manufacture of a wide range of candidate biologics in GMP-compliant facilities.
Development and manufacturing facilities of the highest standard keep Xenovabio at the forefront of contract manufacturing.
Development and manufacturing facilities of the highest standard keep Xenovabio at the forefront of contract manufacturing.
Our highly-skilled workforce is dedicated to making each and every project a success.
Our highly-skilled workforce is dedicated to making each and every project a success.
Our on-site quality control department undertakes extensive testing through a wide range of analytical assays.
Our on-site quality control department undertakes extensive testing through a wide range of analytical assays.

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