This webinar was presented live on Thursday, September 24, 2020. Click below to watch it on demand.
Gaining the right product approvals and certificates for major markets is fundamental to both succeed and to ensure safety and effectiveness of every medical device. Properly defined and prepared submission reports contain the appropriate information required by the various regulatory bodies for the specific product classification. Regulatory Information Management breaks the silo barriers within a company to create a more unified approach to launching a product and “embeds” regulations as an asset, optimizing and controlling the management of highly-regulated business processes for worldwide submissions and approvals.
Attendees of this webinar will learn to:
- Streamline putting a safe and effective device on the market and ultimately improve lives.
- Maintain full control of your registration journey.
- Improve device development and enable regulatory decision-making for the next generation of medical products.
Quality Management Senior Solution Consultant
Manufacturing and Engineering Technology Advocate