| Aesica Pharmaceuticals | ||
We provide a tailored service incorporating integrated project management and working in partnerships on all projects, from individual development and scale-up to large-scale commercial manufacturing and technical transfers. |
We produce a broad range of chemical synthetic compounds including potent chemicals in quantities for use in Phase I to III clinical trials. |
We offer an extensive range of process technologies for manufacturing and packaging of formulated products including solid, semi-solid and liquid dosage forms, anaesthetics and potent drugs. |
We have years of experience in supplying bulk APIs and have built a reputation for reliability, quality and unparalleled service, our API manufacturing facilities have extensive chemical processing capabilities including potency facilities. |
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| Angel Biotechnology | ||
Angel Biotechnology is a contract biomanufacturing company offering process development services and pre-GMP and cGMP manufacturing. |
Angel Biotechnology plans and executes manufacturing strategies for recombinant proteins, cellular therapies and stem cells, antibodies, and viruses. |
The facilities at Pentlands Science Park include fermenters for cGMP production of materials using mammalian cells and for production of material using bacteria, fungi or yeast under cGMP conditions. |
| Arevipharma | ||
Arevipharma develops, optimizes and produces pharmaceutical agents and intermediate products. |
A newly renovated laboratory and a pilot plant are available for chemical and process research towards effective process development and scale-up. |
Arevipharma produces pharmaceutical agents and highly active substances. |
| B. Braun OEM | ||
B. Braun is your professional and reliable outsourcing partner for pharmaceutical contract manufacturing and customised product variation and combination. |
Active in 50 countries worldwide, B. Braun adheres to international production standards and provides a constant high level of quality. |
Partnering with OEM offers a comprehensive product range for infusion therapy, including system components and different container types. |
| Baxter Biopharma Solutions | ||
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 molecules 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. |
Baxter has over 15 years of experience in developing and manufacturing monoclonal antibodies and recombinant proteins. |
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| Bio Concept Laboratories | ||
Bio-Concept Laboratories is an FDA registered contract research organization (CRO) and contract manufacturing organization (CMO). |
Bio-Concept has developed an integrated product development program designed to bring your new product to market, efficiently and effectively. |
At Bio-Concept, we are highly experienced in developing, qualifying, validating, and comprehensively documenting analytical methods for raw materials, process streams, dosage forms and cleaning operations. |
| Cangene | ||
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. |
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. |
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. |
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| CoreRx™ Pharmaceuticals | ||
CoreRx™ Pharmaceuticals is a contract pharmaceutical development and manufacturing organization (CDMO) that helps pharmaceutical and biotechnology companies bring new drugs to the clinic quickly and efficiently. |
CoreRx supports and streamlines the drug development process by offering focused services in the area of pre-formulation / formulation development, analytical development and clinical manufacturing. |
CoreRx offers formulation development services for a variety of dosage forms, as well as catering to the unique dosage development needs of our clients. |
CoreRx develops and manufactures clinical materials with strict quality compliance to cGMPs; CoreRx has innovative manufacturing capabilities for oral solids, liquids and semi-solids, as well as innovative delivery options per client request. |
Our services center on small molecule development and analysis, including pre-formulation, method development and validation, drug substance characterization, finished product release, and stability testing and storage. |
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| Covidien Pharmaceuticals Outsourcing | ||
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 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. |
Facilities undergo regular audits by both regulatory agencies and clients to ensure that quality standards are met and exceeded. |
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| Créapharm | ||
Créapharm is a pharmaceutical contract manufacturer and leading investigational medicinal products supplier. |
MP5 specialises in the development and production of liquid or lyophilized injectables, supplied in vials, bags or syringes. |
Créapharm provides capsule blinding and placebo capsule manufacture; our over-encapsulation capacity is the largest in Europe. |
Créapharm offers primary and secondary packaging for clinical batches of investigational medicinal products. |
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| DPT Laboratories | ||
DPT Laboratories has a 70-year history of developing and manufacturing semi-solid and liquid drug products. |
DPT is a contract development and manufacturing organization that has over 1,000 employees, including over 100 scientists and engineers. |
DPT has five cGMP facilities for the manufacturing of sterile and non-sterile dose forms. |
DPT's drug development services for sterile and non-sterile dose forms benefit from the company's exemplary quality and regulatory history. |
DPT's semi-solid and liquid dosage form manufacturing facilities have GMP certificates from FDA, MHRA and ANVISA. |
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| Dr Reddy's Laboratories SA | ||
CPS delivers unparalleled service, reliability and value to our customers. |
Operating from eight sites located in India, Mexico and UK with US FDA and EMEA approved facilities, CPS has global capabilities. |
An industry-leading portfolio of technologies with specific strengths in chiral chemistry and complex synthesis. |
Specific product expertise in high containment, activated mPEGs, naproxen, steroids, prostaglandins and permethrin. |
A full range of dosage development capabilities from pre-formulation, formulation development, cGMP clinical batch manufacturing, scale up and commercial manufacturing. |
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| Eskayef | ||
State-of-the-art manufacturing facilities for solid dose and injectable dosage forms. |
Fully equipped analytical laboratories for both ICH stability studies and product release. |
Integrated aseptic powder filling line fully compliant with EU GMP Annex 1 requirements. |
| Fresenius Kabi Product Partnering | ||
Fresenius has more than 20 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' 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. |
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| Gesellschaft fur Micronisierung | ||
Micronisation (ultra-fine milling) involves the reduction of particles to a size of less than 10µm, using special milling processes. |
Even sterile products can be micronised under clean-room conditions. |
GfM has been working for well-known pharmaceutical companies in the field of product sterilisation for many years. |
We use a variety of sieving technologies to fractionate your products or carry out protective sieving before or after micronisation. |
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| GIPHARMA | ||
GIPHARMA is a pharmaceutical contract manufacturer for injectable and freeze-dried products, and is Italy’s only pharmaceutical manufacturer specialized in radiopharmaceutical products. |
GIPHARMA offers liquid fill and lyophilization, microbiological and QC analytical testing, chemical and radiochemical analysis, and complete aseptic manufacturing processes for clinical trails materials and commercial batches. |
GIPHARMA can manufacture injectable products requiring either completely aseptical manufacturing process or terminal sterilization; lyophilization batch size can reach 14,000 vials (10ml capacity). |
GIPHARMA offers sterile freeze-dried vials and radiopharmaceutical cold kits, and can manufacture a range of radiopharmaceutical products, including albumin macroaggregates for lung scintigraphy, methylene di-sulphonic acid for bone scintigraphy and mebrophenin for epatobiliary system scintigraphy. |
GIPHARMA supports PET isotope manufacturing centres, with products such as sterile vacuum vials, sterile saline elution vials, sterile alumina columns and sterile disposable components. |
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| GP Pharm | ||
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's developments in biodegradable polymers and liposomal formulations offer improved delivery profiles for cytotoxic and high potent APIs. |
| Halo Pharmaceutical | ||
With over 30 years’ experience in pharmaceutical manufacturing, Halo has the experience and a wide range of granulating, blending, compressing and coating equipment necessary to support our customers. |
Halo has the ability to package solid, liquid and semi-solid non-sterile and sterile dosage forms into a variety of bulk or final packages. |
Halo offers development from pre-clinical to Phase III, and manufacturing services with expertise in the areas of tech transfer, process, product and methods development, production scale-up and validation. |
| Haupt Pharma | ||
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. |
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. |
Isolator technology at Haupt Pharma Wolfratshausen’s sterile department. |
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| Health Protection Agency | ||
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. |
Contract filling for biological products. |
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. |
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| IDT Biologika | ||
Several filling lines for aseptic processing of prefilled syringes. |
The automatically loading and reloading of lyophilisators. |
Labelling, blistering and final packaging of syringes. |
Leading in lyophilisation of narcotics. |
Fill and finish of ampoules, vials, syringes and bottles. |
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| IDT Biologika | ||
We have extensive experience in the development and production of vaccines. |
We perform large scale production of a wide variety of vaccines. |
Manufacture of cell cultures in SPF-eggs. |
State-of-the art technologies for contract manufacturing of viral vaccines. |
IDT was the facility of the year 2008 award winner in Operational Excellence. |
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| Kemwell | ||
Kemwell is a leading pharmaceutical contract development and manufacturing company. |
Kemwell provides expert solutions in pharmaceutical product development, sourcing, analytical support, clinical batch production, and commercial-scale manufacturing and packaging. |
We offer services such as full-service pharmaceutical process development, manufacture, formulation, and fill and finish. |
Whether you are looking for pre-formulation studies, formulation development, stability studies, analytical support, clinical batch production, commercial-scale manufacturing or packaging, Kemwell is your ideal partner. |
We manufacture gels, ointments, creams and solutions for various topical and ophthalmic applications. |
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| Laboratoria Smeets | ||
Mixing activity. |
Filling activity. |
Sachet filling activity. |
Laboratoria Smeets’ laboratory handles contract manufacture and contract packing of pharmaceutical powders and liquids. |
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| Lomapharm® | ||
Our analytical laboratories. |
Blistering line production. |
Our filling lines are designed for filling operations under aseptic and sterile conditions. |
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. |
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| Lonza | ||
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. |
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 is building Asia's most advanced mammalian cell culture manufacturing facility, in Tuas Biomedical Park, Singapore. |
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| Micron Technologies | ||
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. |
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 believe in maintaining the highest standards of Good Manufacturing Practice and complying with the current requirements of the regulatory authorities. |
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| Novasep | ||
Contract biomanufacturing services. |
Custom purification. |
Exclusive synthesis. |
Upstream technologies for biopharmaceutical manufacturing. |
Chemical route optimization |
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| Nycomed | ||
Nycomed provides a range of technologies for the production and packaging of solid and liquid pharmaceuticals. |
It has always been Nycomed’s policy to give patients the best in terms of reliability, quality and responsiveness. With their contract manufacturing services, Nycomed shares this approach with its customers in a strong and economically sound partnership. |
Nycomed Contract Manufacturing Services offers the highest level of customer focus in terms of reliable communications. Clients are linked directly to the operational managers at the manufacturing sites. |
| One 2 One® | ||
One 2 One strives to be a global leader in the small-volume parenteral market, producing high-quality products in glass and plastic vials and ampuls. |
Prefilled syringes are available in luer cone, luer lock and staked-in needle configurations, with or without anti-needlestick devices. |
iSecure is a prefilled unit-dose disposable injection syringe designed for compatibility with IV administration sets and IM injections. |
With expertise in pharmaceutical disperse systems, One 2 One is a clear leader in the development and manufacture of emulsion-based formulations. |
One 2 One's flexible containers are available in a wide variety of sizes and configurations. |
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| PharmaZell | ||
PharmaZell offers drug substance and drug product development and manufacturing services to pharmaceutical innovators and generic companies. |
PharmaZell has decades of experience in the development and commercial manufacture of oral solid dosage forms, APIs, amino acids and advanced intermediates. |
PharmaZell’s GMP-compliant site in Copenhagen has been used for integrated drug developments and API competence for 30 years. |
| PharmIdea LLC | ||
Pharmidea manufacture their sterile solutions and freeze-dried cytotoxic products in an isolator. |
Pharmidea manufacture sterile injectable oncologicals in 1ml – 100 ml vials. |
Pharmidea is located in-between EU and Russia / CIS countries. |
| Polymun Scientific | ||
Your cell line is in good hands at Polymun. |
Our team is experienced in handling sophisticated processes. |
Polymun has a clear understanding of purification. |
Comprehensive documentation is important to us. |
We care for your product. |
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| Rechon Life Science | ||
Rechon is experienced in the development and manufacturing of pharmaceuticals, allowing us to offer any service within the field of small volume parenterals, and oral and nasal liquid products. |
Rechon focuses on contract pharmaceutical services and collaborates with companies of all sizes. |
We produce commercial-scale batches and small-scale batches for development and clinical trials. |
We have experience in the manufacturing of clinical trial materials for all stages of clinical development. |
Rechon can assist you with supplier audits, product quality reviews, QP release, product complaints and other quality and regulatory services. |
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| Recipharm | ||
Recipharm offers formulation development services and commercial manufacturing and packaging. |
Recipharm is one of Europe’s leading pharmaceutical contract development and manufacturing organisations. |
Recipharm has manufacturing facilities in Sweden, France, Switzerland and the UK, some of which are FDA accredited. |
Recipharm takes a joint risk and reward approach to projects, and can offer customised services. |
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| Ropack | ||
Ropack offers high-speed blister manufacturing of solid oral dosage, as well as custom blister packaging for capsules and tablets. |
Our pharmaceutical contract manufacturing services include capsule filling and tableting. |
Ropack is an ideal partner in pharmaceutical formulation development. |
Ropack provides warehousing and distribution services for commercial products and clinical trial materials. |
Ropack offers custom primary and secondary packaging for clinical trials, sales and physician samples and commercial launch. |
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| ROVI | ||
Contract manufacturing facilities in Madrid, Spain. |
Pre-filled syringes of 0.2ml to 5ml. |
Pre-filled vials of 2ml to 20ml. |
Clean areas for aseptic filling. |
Visual inspection system for pre-filled syringes and vials. |
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| Sanochemia Pharmazeutika AG | ||
Sanochemia Pharmazeutika is a service provider for API synthesis and contract manufacture of final dosage forms. |
Sanochemia can contract manufacture from gram-scale to commercial manufacturing volumes in a cGMP-compliant plant for active pharmaceutical ingredients. |
Our service range includes packaging material sourcing, manufacturing and batch release. |
Our qualified team of chemists can undertake comprehensive pharmaceutical analysis of APIs and finished products using standard chromatographic methods and standard microbiological methods. |
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| SBH Sciences | ||
SBH Sciences provides preclinical process development services, including cell culture (mammalian and insect cell), protein purification, cell-based assays and ELISA development kit services. |
Our array of cytokine bioassay services is the most comprehensive in the US, and our proprietary processes have achieved commercial production of 30 monoclonal antibodies and over 24 highly purified recombinant cytokines. |
We offer in vitro cytotoxicity testing, and we can perform any non-radioactive cytotoxicity assay, order any new cell line and custom-develop your assay according to your needs – contact us with any request for cell-based toxicity testing. |
| Symyx | ||
Process development: quickly identify and optimize key process conditions and parameters to speed and ensure successful development. |
Formulation studies: optimize liquid, solid and lyophilized formulations for improved delivery, and investigate the effect of excipients on drug substance and other parameters. |
Preformulation studies: investigate the physical and biological properties of a molecule, identify key stresses and degradation products, create stability indicating assays, and select the feasible formulation for early clinical trials. |
CGMP fill and finish: deliver liquid and lyophilized drug product in quantities suitable for preclinical and early clinical supply. |
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| Therapex | ||
Therapex provides outsourced drug development and manufacturing services, and has over 40 years of experience in the contract manufacture of semi-solid and liquid products. |
Therapex has expertise in the contract manufacture of oral liquid and topical health care products, and can offer product development, technology transfer, commercial manufacturing and packaging, product and process validation, analytical chemistry, microbiology, test method development and validation, ICH stability and FDA regulatory compliance. |
Therapex provides its customers with comprehensive stability programs for formulation evaluation, clinical supplies and commercial finished products, including study protocols, summary reports and recommendations for shelf life. |
Therapex has a fully equipped cGMP compliant chemistry and microbiology laboratory for contract manufacture of semi-solid and liquid products. |
Therapex manufactures oral and topical (prescription and OTC) solution, dispersion and suspension products such as syrups, antacids, laxatives, nasal sprays, medicated shampoos, sunscreens and acne treatments. |
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| Unither | ||
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. |
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. |
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| Vetter Pharma International | ||
Patient-friendly, pre-filled application systems. |
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 European Outsourcing Awards. |
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| Wockhardt | ||
Meet Mark and learn more about our know-how. |
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. |
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. |
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