Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation
- Frank Stein
- Virtual Seminar | March 8-9, 2021
Laboratory Inspection and Auditing
- Mark Powell
- Virtual Seminar | March 9, 2021
Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in ....
- Haja Sittana El Mubarak
- Virtual Seminar | March 11-12, 2021
Implementing UDI (Unique Device Identification) - Plan Now for Success
- Lena Cordie
- Virtual Seminar | March 16, 2021
PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation
- Cynthia Brysch
- Virtual Seminar | March 18-19, 2021
REACH and RoHS Compliance: Gain a Deeper Understanding
- Kelly Eisenhardt
- Virtual Seminar | March 18-19, 2021
21 CFR Part 11 Compliance for SaaS/Cloud Applications
- David Nettleton
- Virtual Seminar | March 23-24, 2021
Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR
- David Nettleton
- Virtual Seminar | March 23-24, 2021
Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing
- Joy McElroy
- Virtual Seminar | March 24-25, 2021
Regulatory Compliance for Dietary Supplements in the US, EU and Canada
- Travis Austin MacKay
- Virtual Seminar | March 24-25, 2021
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
- Mark Powell
- Virtual Seminar | March 25-26, 2021
Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
- David L Chesney
- Virtual Seminar | March 29-30, 2021
