Courses - Eventura.site

Risk Management using Lean – Are you sure your documents are clutter free?

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

Quality Risk Management Overview

Ensuring your Site is Ready for an FDA Inspection

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