Webinar Highlights
Is your company’s recall processes and safety protocols aligned with the latest relevant laws?
Secure your spot! Register for “The Top Recall Regulatory Shifts and Industries Impacted in 2022” live webinar September 27th, 2022 @ 11:00AM CT with Live Q&A.
Get expert insight to help your organization plan for the latest regulations and recall regulatory trends in 2022.
Regulators continue to grapple with challanges from the ongoing pandamic, chaotic geopolitical events, global inflation, and ongoing supply chain challenges. As law firms, insurance companies and communications firms plan for new regulations, this webinar will enlighten and help focus on what’s happening today and what is on the horizon as it relates to medical device, pharma, food and drink, and consumer products.
Host: Dr. Darin Detwiler, LP.D.
Special Guest: David Mahoney, JD
Time: 11:00A – 12:00P CT
Topics & Questions Covered:
Highlight: Legal changes and challenges in recent law changes, landmark changes, and more.
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- How changes in consumer behaviors and web purchases have created challanges and changes in recall compliance laws.
- Where the laws are changing
- Legal aspects of recalls
- Timelines of changes in laws
- Consquences – How these laws apply to recalls
- Examples
- Challanges ahead
- Live Q&A
(Even if you can’t join live, register now and we’ll send you the recorded webcast and podcast to watch or listen to at your convenience.)
Who Will Benefit
Personnel who are responsible for overall recall decisions and/or execution, particularly:
- Regulatory personnel
- Quality personnel
- Aspiring regulatory and quality leaders/senior leaders
- Members of recall Teams (from functional areas such as Operations, Service and Marketing)
This webinar will focus on how the demand on distribution channels has drastically changed, online consumer behavior and social medial influencers have effected corporate behavior and expedited recall compliance laws, and how FDA regulated items have also led to changes in responses and regulations.
TOPICS & QUESTIONS COVERED:
Highlight: Legal changes and challenges in recent law changes, landmark changes, and more.
- How changes in consumer behaviors and web purchases have created challanges and changes in recall compliance laws.
- Where the laws are changing
- Legal aspects of recalls
- Timelines of changes in laws
- Consquences – How these laws apply to recalls
- Examples
- Challanges ahead
- Live Q&A
Mock Recalls.com is dedicated to helping companies meet the necessary recall readiness requirements. Don’t miss this important opportunity to learn from recall industry experts, Dr. Darin Detwiler and guest David Mahoney, JD as they highlight the latest regulatory changes coming in 2022 and what to watch out for in the coming months.
Host: Dr. Darin Detwiler, LP.D.
Dr. Darin Detwiler is an author, advisor, consultant, and an Associate Teaching Professor of regulatory policy and corporate social responsibility at Northeastern University’s College of Professional Studies in Boston. His students have gone on to leadership positions in industry and in state and federal agencies. For nearly 30 years, he has played a unique role in controlling foodborne illness. Detwiler collaborated with the Secretary of Agriculture on USDA consumer education in the early 1990s, then served two appointed terms on the USDA’s National Advisory Board on Meat and Poultry Inspection. He has impacted FDA policy as the Senior Policy Coordinator for STOP Foodborne Illness, through service on Conference for Food Protection councils, and through his work with the FDA. Detwiler’s research and insights have appeared on television, industry magazines, and in books. He sits on numerous advisory and editorial boards and has long consulted on policy with industry in the U.S. and abroad. Dr. Darin Detwiler is the recipient of the International Association for Food Protection’s 2022 Ewen C.D. Todd Control of Foodborne Illness Award as well as their 2018 Distinguished Service Award. He is also a recipient of an AMGEN Biotechnology 2009 AASTE Award.
Guest: Dr. Stephen Amato, PhD
Dr. Stephen F. Amato has over 25 years of experience in the pharmaceutical, biotechnology and medical device industries. Prior to his position as Faculty Director of Graduate Regulatory Affairs and Life Sciences at Northeastern University, Steve was the Founder and Managing Director of tJun17 Life Sciences Advisors, LLC, and also a Managing Director for Cardinal Health Regulatory Sciences. Additionally, as an Executive with GfK Health, Dr. Amato managed and worked on client global regulatory affairs and reimbursement projects in the areas of market access, pricing, and payer coverage, coding and payment strategy. Prior to GfK Health, as an Executive Director at Anika Therapeutics, Steve managed all aspects of the company’s product portfolio including regulatory, reimbursement, market segmentation, targeting, positioning, pricing and promotional strategies. Dr. Amato’s research has been published in the Journal of Immunology and Cancer Research. He co-edited and wrote several chapters for the book, Regulatory Affairs for Biomaterials and Medical Devices, published by Elsevier Publishing in 2015.
Steve holds an AB in Biochemical Sciences from Harvard University, a Ph.D. in Molecular and Cellular Biology from Boston College’s Graduate School of Arts and Sciences, and an MBA from the Carroll School of Graduate Management at Boston College. He has also received the U.S. and EU Regulatory Affairs Certification designations and is a Consultant for the Regulatory Affairs Professional Society.