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EU MDR Implementation and Transitioning to the Deadline: Essential Tasks to Complete
MP3 Download This 2-day virtual seminar will go into the specifics of the European Union Medical Device Regulation (EU MDR), provide case studies and share le
- Course
- By Kelly Thomas
21 CFR Part 11 and Annex 11; what you need to know to pass the new regulatory inspections
MP3 Download describes exactly what is required for compliance with Part 11
- Course
- By David Nettleton
Clinical Data Management Training
MP3 Download Duration 2 Day
- Course
- By Elaine Eisenbeisz
Dealing with CAPA- Corrective and Preventive Actions in FDA Regulated Industries
MP3 Download New Root Cause Analysis Techniques and CAPA Management live webinar is for those in Operations, Facilities , Engineering and QA/QC
- Course
- By Meena Chettiar
FDA's Recent Regulation on the Use of Social Media
MP3 Download -Duration 90 Minutes
- Course
- By Carolyn Troiano
How FDA trains its investigators to review CAPA and what should you do to prepare
MP3 Download This webinar will discuss all the documents used by FDA to train their inspectors to review your CAPA system, some of which you may not be familiar
- Course
- By Jeff Kasoff
Regulatory Requirements for Registration of Medical Device Products in China
On Demand Webinar Duration 60 minutes
- Course
- By David R. Dills
The Microbiology of Water in a GMP Environment; USP, EP, JP and FDA Requirements for Potable Water, Purified Water, Water for Injection and Steam
MP3 Download This webinar will examine a variety of issues surrounding water in a facility to include the testing of each water source.
- Course
- By Barry A. Friedman