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Informa

19–21 May 2020
Dublin, Ireland

New Global Regulations, Technology Advances and Industry Case Models for Developing, Implementing and Deploying Validation Procedures Enterprise-Wide

Industry’s flagship and best attended global event provides an end-to-end roadmap for compliance in a complex and highly regulated environment.

Take Advantage of our Advanced Pricing Discount...

Register by 13 March 2020 and Save €235!

What to Expect

Validation Strategy
  • Lifecycle Approach To Validation And Qualification
  • Development of Universal QRM Certification Standards
  • Validation of Automated Manufacturing Systems
Laboratory Best Practices
  • Compliance Culture in Laboratory Operations
  • Best Practices for Stability and Forced Degradation Studies
  • Documentation Practices for Successful Operations
EMA Regulatory Guidance
  • Strengths and Weaknesses of Annex 1 — What to Expect
  • Relevant Analysis of ICH Guidelines for QC and Quality Regulations
  • How to Respond to Regulatory Inspection Findings

Build a Customised Itinerary to Align with Your Area of Focus:


3 Inclusive Workshops

6 Interactive Content Offerings

8 Opportunities to Expand Your Validation Network

10 In-Depth and Advanced Sessions