Medical Device Design: FDA Requirements for Data Management

29 Jan 2021 (Fri) - 2:00 to 4:30pm (ON-SITE SEMINAR)

As the COVID-19 pandemic continues to unfold, MedTech companies are focusing on reducing risk and building resilience. Medical device manufacturers are driven by a need to manage information digitally while ensuring the authenticity, integrity, confidentiality, traceability, security and compliance with stringent regulations.

Join our FREE on-site seminar and find out how SOLIDWORKS PDM Professional can simplify the entire process of developing medical devices while complying with the recent FDA regulations.

2:00 - 2:40 PM - Challenges faced by Medical Device Manufacturers by Dassault Systèmes
2:40 - 3:00 PM - FDA Regulations (The 4-Phase Documentation Guidelines)
3:00 - 3:20 PM - Tea Break w/ light refreshments
3:20 - 3:40 PM - Customer Success Story from a Medical Supply Manufacturer Company
3:40 - 4:15 PM - SOLIDWORKS Solutions
4:15 - 4:30 PM - Open Forum / Sharing Session / Q&A