Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
- Mark Powell
- Virtual Seminar | July 6-7, 2020
Writing and implementing a Standard Operating Procedure (SOP) in a Compliant Laboratory (US FDA, US EPA and OSHA Focus)
- John Fetzer
- Virtual Seminar | July 9-10, 2020
Data Integrity: FDA/EU Requirements and Implementation
- Mark Powell
- Virtual Seminar | July 9-10, 2020
Preparing for FDA's New Import/Export Trauma in 2020
- Casper Uldriks
- Virtual Seminar | July 16-17, 2020
Quality Control Laboratory Compliance - cGMPs and GLPs
- Kelly Thomas
- Virtual Seminar | July 16-17, 2020
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
- Barry A Friedman
- Virtual Seminar | July 16-17, 2020
Change Control Best Practices - Avoiding Unintended Consequences of Changes
- Andrew Campbell
- Virtual Seminar | July 27-28, 2020
Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
- Rita Hoffman
- Virtual Seminar | July 22-23, 2020
Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
- David L Chesney
- Virtual Seminar | July 29-30, 2020
