Episode 17 – 4 experts, 120+ years of drug substance experience: major trends you should know

The market for the manufactured and supplied APIs is changing continuously, and there are many factors influencing these changes. Being aware of these changing trends is important. Perhaps what’s even more important is how you leverage the opportunities they bring and how to react to them. In this episode, Ed, Meranda and Brian talk with a group of drug substance services experts about the major trends you should know and be aware of, and how you can use them to your advantage. This panel includes experts who have appeared on the podcast before: David Blasingame, Jim Mencel, Dave Adams and Daniel Torok.

Run time: 35:05mins

Episode 17 – 4 Experts, 120+ Years of Drug Substance Experience: Major Trends You Should Know

Video Credit: DSI, a PLG Company

Takeaways:

01:03 – Ed, Brian and Meranda welcome to the show a panel of drug substance services experts, Daniel Torok, Dave Adams, Jim Mencel and David Blasingame who speak to trends they’ve observed in the landscape of API manufacturing

07:04 – The panel speaks to the types of drug manufacturing requests they’ve been seeing

14:42 – The panel expresses their shared concerns over the diminishing number of API manufacturing professionals in the United States

23:53 – The panel provides their thoughts on the immediate future of API manufacturing

30:04 – The panel discusses the current state of regulation

33:15 – Ed, Brian and Meranda thank the panel for joining the show

About CMC Live

FDA CMC regulations and guidance simplified through examination, real life experiences and risk-based advice. This podcast hopes to educate sponsors and individuals on agency related regulatory CMC matters. We will focus on the critical CMC issues and build programs that enhance drug development. CMC topics will include Regulatory Starting Materials, API and Drug Product Process, Formulation Development, Supply Chains, Analytical Controls. Advocating and interpreting CMC Strategy, directing CMC Operations and Quality Assurance oversight in conjunction with developing CMC submission content that represents the best interests of emerging biotech. NOT INTENDED TO BE PRESCRIPTIVE ADVICE BUT RATHER INTERPRETATION THAT IS RIGHT FOR YOU. Since 2007 we have provided our partners with innovative strategies and exceptional advice intended to enhance program development, product approval, and marketing presence.

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