May 4, 2022 | 12 PM ET | 1 hr
About This Event
Even during COVID-19, U.S. Food and Drug Administration (FDA) inspections carried on. However, quality assurance inspections weren’t the only way the FDA ensured quality. The agency used a number of remote tools to interact with pharmaceutical and medical device companies before performing an inspection or deciding it could wait. Join us for a webinar discussing these tools and how the FDA has changed its processes.
Key Takeaways
- The remote tools that the FDA uses to interact with pharmaceutical and medical device companies.
- Why audit management systems and quality software help with inspections.
- How the same tools that help with inspections help with quality assurance audits.
Meet Our Presenters
Nate Henriod | Senior Product Manager | MasterControl Inc.
Nate Henriod has over 20 years of experience in the biologics and medical device fields including orthopedics, vascular access, wound care, and burn treatment with a focus in product development. He has extensive experience with engineering and quality management system (QMS) software. In his current role as Senior Product Manager at MasterControl he works with beta customers to build the Advanced Quality Event Management (QEM) product. Nate has a degree in chemistry from the University of Utah.
Peter Harris | Senior Product Manager | MasterControl Inc.
Peter Harris
Senior Product Manager
MasterControl Inc.
Peter Harris has over seven years of experience developing products in the medical device industry. Additionally, he has worked for 12 years creating cutting-edge software products for the health care, medical device, eCommerce, and blockchain industries. His current role as Senior Product Manager is focused on creating a delightful communication platform in MasterControl that enables its users to have total awareness and control over their processes as they happen.
Peter has degrees in molecular biology and Korean from Utah State University
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