FDA's Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering
- Theodore Sand
- Virtual Seminar | August 3-4, 2020
REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance
- Kelly Eisenhardt
- Virtual Seminar | August 6-7, 2020
Essentials Of USP Microbiology - Reading Between the Lines of the USP General and Information Microbiology Chapters
- Barry A Friedman
- Virtual Seminar | August 6-7, 2020
Enterprise Risk Management (ERM)
- Richard Barr
- Virtual Seminar | August 10-11, 2020
Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing
- Joy McElroy
- Virtual Seminar | August 18-19, 2020
Regulatory Compliance for Dietary Supplements in the US, EU and Canada
- Travis Austin MacKay
- Virtual Seminar | August 19-20, 2020
Method Development and Validation for Assays Supporting Testing of Biologics
- Gwen Wise Blackman
- Virtual Seminar | August 20-21, 2020
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
- Barry A Friedman
- Virtual Seminar | August 24-25, 2020
REACH and RoHS Compliance: Gain a Deeper Understanding
- Kelly Eisenhardt
- Virtual Seminar | August 24-25, 2020
The Life Cycle Approach to Cleaning Validation
- Joy McElroy
- Virtual Seminar | August 25-26, 2020
Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
- Casper Uldriks
- Virtual Seminar | August 27-28, 2020
The Veterinary Drug Approval Process and FDA Regulatory Oversight
- Mark Hughes
- Virtual Seminar | September 24-25, 2020
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
- Mark Powell
- Virtual Seminar | October 8-9, 2020
