MedTech Primer: Getting Your Product to Market While Avoiding Pitfalls in 2017 and Beyond
Learn regulatory and quality principles in a half day event presented by Life Sciences PA on Wednesday, February 22nd. Member organization Regulatory and Quality Solutions (R&Q), along with a few other special guests, will be presenting content on reimbursement, regulatory, quality systems, design assurance, product quality, and perhaps most important, what specifically to watch for in 2017.
Date: Wednesday, February 22nd
Time: 1:30pm – 4:30pm
*This event will be followed by a complimentary cocktail reception
Agenda
1:30 – 1:35 PM: Program Introduction- Life Sciences PA
1:35 – 2:00 PM: Regulatory & Pitfalls - Jon Gimbel, Director of Western PA Operations, R&Q
2:00 – 2:35 PM: Quality Systems, Post-Market Surveillance and Pitfalls - Jake O’Donnell, Senior, FDA Compliance Principal, R&Q
2:35 – 3:00 PM: Design Assurance and Pitfalls - Jon Gimbel , Director of Western PA Operations, R&Q
3:00 – 3:10 PM: BREAK
3:10 – 3:35 PM: Product Quality and Pitfalls - Ryan Kasun, Project Engineer
3:35 – 4:00 PM: Reimbursement and Pitfalls - Edward Black, President, Reimbursement
Strategies
4:00 – 4:30 PM: What to watch for in 2017: Review of topics trending – Maria Fagan, Cofounder & President, R&Q and Jake O’Donnell, Senior FDA Compliance Principal, R&Q
4:30 – 6:30 PM: Helomics Introduction and CLIA Lab Tour / Networking / Happy Hour
Who Should Attend?
- Early Stage Companies
- Junior and Mid-Level Regulatory and Quality Staff
- Medical Device Development and Manufacturing