| Axeon Corporation » eCourses » On Demand E Learning » Medical Device Regulations- FDA 21 CFR 820

Price: $400.00

The medical device industry is highly regulated due to the product risk to health. One of the regulated requirements is to establish and maintain a quality management system . Although the rest of the world complies with ISO 13485 standard, the United States requires compliance to the 21 CFR 820, Quality System Regulation (QSR).

The QSR, specifying current Good Manufacturing Practices (GMP) for medical devices, was established in 1997 based on earlier structure of the ISO 9001 and 13485.
Understanding the QSR is essential to ensure compliance to the United States regulatory requirements and to prepare for an eventual visit from the FDA.

OBJECTIVES

This course will provide participants with the following:
• Overview of the FDA and intention of the 21 CFR 820
• Up-to-date requirements of the 21 CFR 820
• Working knowledge in application to their organization
• Ability to prepare and host an FDA inspection

Course Length- 8 Modules

Time to complete- 5-7 hours

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