White Papers

Dispelling the Myths of Deviation and CAPA Systems

NSF Health Sciences, Pharma Biotech

'How to Simplify for Improve your Deviation and CAPA Systems' is one of NSF's most popular in-house courses. The company provides simple tools and techniques that dramatically improve efficiency, while also dispelling some myths. Here is a sample of ...

Dispelling the Myths of Deviation and CAPA Systems

Cleanroom Proper Gowning Procedure

Meritech

Ways your personal protection equipment is worn prior to entering a cleanroom environment is critically important to prevent contamination and minimise dispersion of particles and microbes naturally carried on the skin.

Cleanroom Proper Gowning Procedure

STYL'One Evolution - R&D Scale-Up and Production Support

Medelpharm

Medelpharm presents the STYL'One tableting instrument, an all-in-one multi-functional tool for use in all stages of drug development from early formulation to scale-up at production speed.

STYL'One Evolution - R&D Scale-Up and Production Support

Weibel CDS: Safer, Easier, and Faster Drug Delivery

Weibel CDS

At the Advanced Technologies and Treatments for Diabetes (ATTD) congress in Paris, Weibel CDS showcased a presentation demonstrating its patient-centric drug delivery products, which help reduce contamination, handling errors, and needle stick injuri...

Weibel CDS: Safer, Easier, and Faster Drug Delivery

Quality is the Foundation of Efficiency

Delta 2000

Worldwide leading designer and producer of clean room solutions Delta 2000 was founded by the merging of two companies, which had served various markets for more than 20 years.

Quality is the Foundation of Efficiency

Flexible Drug Containers for Parenteral Drugs

Weibel CDS

Self-medication is becoming more popular, driven by cost considerations. Valuable time of healthcare personnel and the high cost of hospital stays are outweighing the costs of treatment drastically.

Flexible Drug Containers for Parenteral Drugs

Fitoclima Walk-In Stability Storage Room Brochure

Aralab

Aralab offers a range of temperature and humidity controlled storage and environment rooms designed for stability studies, shelf-life assessments, and package testing.

Fitoclima Walk-In Stability Storage Room Brochure

Reusable Cleanroom Coveralls: Improving the Sustainability Scorecard

Prudential Cleanroom Services

Cleanroom coveralls are an essential component in facilities for the bioprocessing, life sciences, and semiconductor sectors.

Reusable Cleanroom Coveralls: Improving the Sustainability Scorecard

Aralab Stability Product Brochure

Aralab

Aralab specialises in designing, developing, manufacturing, and servicing environmental chambers and controlled environment rooms.

Aralab Stability Product Brochure

Patch Pump Applications

Weibel CDS

Treatments for pain or oncology drugs often use pump systems in the beginning. However, not only is time and cost of the essence, the potential of an overall increased treatment result combined with lower side-effects is more and more considered for ...

Patch Pump Applications

Rules for Investigating Good Manufacturing Practice (GMP) Deviations in Sterile Processing

NSF Health Sciences, Pharma Biotech

When things go wrong, there are five non-negotiable processes that should be defined on your deviation investigation standards of practice (SOP): immediate engagement, gemba, triaging using a documented risk assessment, using the Klein process to det...

Rules for Investigating Good Manufacturing Practice (GMP) Deviations in Sterile Processing

Applications in Pharmaceutical Manufacturing

Alconox

The use of aqueous cleaning in pharmaceutical manufacturing can provide numerous benefits in terms of effectiveness, minimal surface residue, and easier cleaning validation.

Applications in Pharmaceutical Manufacturing

The Costs of Over-Complexity

NSF Health Sciences, Pharma Biotech

In this whitepaper, Martin Lush discusses the issue of over-complexity in the pharmaceutical industry.

The Costs of Over-Complexity

Cleaning Validation for Pharmaceutical Manufacturing

Alconox

Cleaning validation is a requirement for pharmaceutical manufacturing, which adheres to current good manufacturing practice (cGMP) and quality systems regulations (QSR).

Cleaning Validation for Pharmaceutical Manufacturing

Case Study: Assessing Potential for Oral Delivery Using Parallel Screening

Catalent

Catalent utilised two technologies targeting duodenal and sublingual biological barriers through a parallel screening approach to assess the oral delivery potential of Salmon Calcitonin.

Case Study: Assessing Potential for Oral Delivery Using Parallel Screening

Case Study: Formulation Prototypes with Increased Solubility and Bioavailability

Catalent

Catalent Pharma provided London-based pharmaceutical company Trio Medicines with three formulation technologies and four prototypes showing improved solubility and bioavailability for an acetyl prodrug of a novel, well-tolerated G-protein coupled rec...

Case Study: Formulation Prototypes with Increased Solubility and Bioavailability

Take the Challenge: Replace Disposables with Reusable Healthcare Textiles

Prudential Cleanroom Services

Make a contribution to healthcare cost control by investing in reusable gowns, scrubs, uniforms, linen, drapes, curtains, and other reusable textiles. This reduces waste and contributes significantly to efforts to reduce the cost of care.

Take the Challenge: Replace Disposables with Reusable Healthcare Textiles

Want to Change Your Quality Culture?

NSF Health Sciences, Pharma Biotech

Despite lots of effort, most change initiatives fail because behaviour of the masses remains unchanged.

Want to Change Your Quality Culture?

China Biopharmaceutical and Pharmaceutical Regulatory Framework Reforms

CPhI China

The China Food and Drug Administration has noted a number of reforms to biopharmaceutical and pharmaceutical policy frameworks, aiming to encourage development, approval, and manufacture of required therapies.

China Biopharmaceutical and Pharmaceutical Regulatory Framework Reforms

Enhanced Sterility Assurance in Stopper Processing

Sartorius

Stoppers for pharmaceutical primary packaging must preserve the safety and efficacy of injectable drugs.

Enhanced Sterility Assurance in Stopper Processing

Micronisation and Milling

FPS Food and Pharma Systems

FPS is specialised in fine size reduction equipment and containment systems for many industrial applications.

Micronisation and Milling