Establishing Effective Employee Training Programs for Medical Device Companies: What Works and What Doesn’t

This webinar will focus on how to establish an effective training program, at medical device companies, that will not only prepare you for an FDA inspection but will also enhance your overall business performance.

Why Should You Attend:

The USFDA requires that device manufacturers train their personnel. The requirement for training for medical device firms is contained in 21 CFR 820.25(b). During agency inspections, the investigator will check training records to see that your firm’s training program is adequate.

Areas Covered in the Webinar:

• Overview of Regulation.
• Review of recent Warning Letters.
• What’s expected by the FDA.
• What doesn’t work and why.
• What works and why.
• FDA readiness.
• Business efficiency

Who Will Benefit:

• Quality System Professionals
• Quality Assurance
• Company Training Coordinators
• Operations Supervisors and Managers