Are you ready to enter the U.S. market?

To enter the U.S. market, manufacturers of medical devices, including in vitro diagnostics, must understand FDA’s good manufacturing practices, which are described in the Quality System Regulation 21 CFR 820, and they must implement all applicable sections.
This seminar is perfect for professionals who are learning about entering the US market for the first time or for those who want to refresh their existing knowledge.

Note: This seminar will be held in French.

Seminar Contents

• Basics of the Quality System Regulation (QSR).
• All sections of 21 CFR 820 (Subparts A through O)

For multiple attendees, we can also conduct on-site seminars.
Please contact seminar@kenblockconsulting.com for further information.