Courses - Eventura World

3-Hours Virtual Seminar – Technical Writing for the Regulated Industries

Quality Risk Management Overview

Ensuring your Site is Ready for an FDA Inspection

Statistical Process Control (SPC) and Control Charts for Laboratory Compliance

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