Courses - Eventura World us

CE Marking in the EU – Latest Regulations

Writing Followable Procedures – Avoid Procedure Related Deviations

Trial Master File (TMF) – Clinical Trial Systems and FDA Expectations

RISK-BASED CLEANING VALIDATION

Layered Process Audits for USFDA Regulated Industries

3-Hour Virtual Seminar on Statistical Process Control (SPC), Process Capability, and Non-Normal Distributions

Risk based approach to GxP Compliant Laboratory Computerized Systems

The New EU Medical Devices Regulations Training - Essential Tasks to Complete the EU MDR Implementation and Transition

ICH Q7 – GMPs for Active Pharmaceutical Ingredients

3-Hour Virtual Seminar on Validation and Part 11 Compliance of Computer Systems

COMPUTER SYSTEM VALIDATION FOR CLOUD AND COTS APPLICATIONS

Artificial Intelligence in Pharmaceutical GMP Operations - Case Studies