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The packaging used in a drug product contributes towards the protection of the drug and maintenance of the drug’s stability. To ensure patient safety and drug compliance, a suitable containment system needs to be carefully selected, based on the drug’s properties, route of administration and intended patient group. The applicable regulatory requirements and compendial compliance are also key considerations during the initial drug development phase. In this webinar, West will be sharing more about the various packaging systems, the challenges faced by pharmaceutical manufacturers and solutions to mitigate the risk. Regulatory expectations on extractables and leachables, as well as insights over the China Drug Master File (DMF) system will also be discussed. The webinar will be presented in Chinese and all colleagues in the pharmaceutical industry are welcome to join.