The aim of this webinar is to promote the fight against IP Crime in the area of Counterfeiting and Pharmaceutical Products.
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Various ways to implement continuous manufacturing in pharmaceutical development and production
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Leachable risk management continues to be of regulatory interest. However, we continue to rely on experimental extractable studies as predictors of leachable risk. These are complex to design and implement and do not always offer the answer to what is the leachable risk for a drug product or medical device.
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quotientsciences
Many pharma companies are seeking new ways of making drug development more efficient and cost-effective through innovation, new technologies and process evolution. This has led to an increase in the outsourcing of development activities to contract research partners who focus solely on disciplines such as discovery chemistry, clinical testing, and formulation development and manufacturing.
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