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004 Quality Assurance and Auditing in the Age of Covid-19 - Bettina Kaplan

004 Quality Assurance and Auditing in the Age of Covid-19 - Bettina Kaplan

FromCMC Live - Chemistry, Manufacturing & Controls


004 Quality Assurance and Auditing in the Age of Covid-19 - Bettina Kaplan

FromCMC Live - Chemistry, Manufacturing & Controls

ratings:
Length:
33 minutes
Released:
Aug 21, 2020
Format:
Podcast episode

Description

What We Covered02:08 – Bettina Kaplan joins the show to discuss her background in quality assurance, compliance and auditing within the pharmaceutical industry09:43 – Trends in quality auditing that Bettina observed before the shutdown and strategies to ensure a successful audit12:48 – Bettina expounds on when it’s appropriate to have an expert, such as an analyst or a drug substance chemist, present during an audit14:42 – Bettina speaks to challenges that Covid-19 has posed to auditing and how she would prepare for a virtual audit19:48 – Risks and dangers associated with not having regular audits during Covid-19 and the importance of having flexibility as an auditor24:36 – Bettina discusses the evolution and growing acceptance of virtual audits in the pharmaceutical industry, including potential benefits and disadvantages30:05 – Ed, Brian and Meranda thank Bettina for joining the showTweetable Quotes“The person [auditor] needs to be able to communicate properly. So, build a rapport with the auditee. When you build that rapport, auditees tend to tell you more than just your basic questions.” “So, if you have to cover manufacturing, analytical and all the quality systems in one day to do a thorough audit, there’s no way you can do it with just one person. You need to have the other experts.” “The other issue is going to an audit. If you’re from a location like where I live, I have to be in quarantine for two weeks before I can even go into an audit. And then I have to be in quarantine for two weeks after. It’s not feasible. And there are a lot of states like that where we have personnel that need to be able to audit and they can’t.” “How do you get the site that you’re auditing to work with you? It’s showing them that you’re willing to work with them.” “A paper audit is never as effective as a virtual or on-site audit. A paper audit a lot of times can be used in conjunction with the on-site or virtual audit.” Relevant LinksLeadershipDesign Space InPharmatics - LinkedInDesign Space InPharmatics - TwitterEdward Narke on LinkedInBettina Kaplan on LinkedIn
Released:
Aug 21, 2020
Format:
Podcast episode

Titles in the series (27)

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.