This webinar covered the following topics:
- Navigating an ambiguous regulatory path to meet current good manufacturing practice requirements
- Setting an internal quality and regulatory strategy for a combination product portfolio
- Combining skill sets to overcome knowledge gaps between the device and pharmaceutical disciplines
- Using post-launch usability evaluation techniques to eliminate usability issues in product revisions
- Foreseeing industry implications as a result of rapid combination product development growth
Speaker:
Khaudeja Bano, MD
Senior Medical Director, Medical Device Safety Head
AbbVie
Contact:
Brooke Akins | Manager, Market Intelligence | 312.224.1693 webinars@q1productions.com
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