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By Dr. Bettine Boltres

August 24, 2020

Putting together a risk assessment for nitrosamines in your final drug product is an extensive undertaking. Many contributing factors need to be considered, such as the drug substance’s manufacturing process, excipients, buffers, water, production equipment and environment, transportation conditions, packaging, and more. Within this scope, primary packaging components, such as elastomeric closures, also could contribute nitrosamines or precursors.

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By Varun Gupta

January 25, 2019

West presented a webinar: Navigating Particle Challenges in Sterile Drugs from Component to Patient by Fran DeGrazio, Vice-President, Scientific Affairs & Technical Services, and John Rech, Technology Manager – Particles, Analytical Lab Services, LLC.

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By West's Global Communications Team

May 06, 2015

How can your packaging and delivery system meet the requirements of the drug product, the expectations of the end user and the demands of regulatory agencies all at the same time?

Start with the end in mind.