Courses #Virtual Seminar - Eventura World us

Developing Effective Post Market Surveillance and Complaint Handling Requirements (Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls)

Good Manufacturing Practices (GMP) 101

FDA Inspections Seminar for 2024

Design of Experiments 101 - Methods and Analysis

3 Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries

3-HOUR CERTIFICATION COURSE ON GOOD MANUFACTURING PRACTICES (GMP) – AN INTRODUCTION

3-Hour Virtual Seminar On Root Cause Analysis, CAPA And Effectiveness Checks

3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out

3-Hour Virtual Seminar on Master Validation Plan – The Unwritten Requirements

3-Hour Virtual Seminar on Effective Cleaning Validation Procedures – Best Practices

3-Hour Virtual Seminar on Successful Deviation Investigations

3-Hour Virtual Seminar on Complaint Handling and Medical Device Reporting and Recalls