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Implement Critical Processes that Align with New FDA and Global Regulations

March 28-30, 2017
  • Amsterdam, The Netherlands

IVT’s premier Data Integrity Validation Europe conference provides the tools you need to build a compliant data integrity program that adheres to cGMP protocols, as determined by global authorities, to prepare for your next inspection. Gain insight into FDA’s new draft guidance, as well as direction from MHRA and WHO. Benchmark against industry peers to ensure quality control throughout your organisation and avoid FDA warning letters and other fines that lead to loss of time, money and reputation.

BENCHMARK BEST PRACTICES FOR EXECUTION
WITH DATA INTEGRITY COMPLIANCE:

  • Ensure Compliance with Computer Systems
  • Reduce Risks and Enhance Reliability of Results
  • Develop a Lifecycle Approach to Ensure Compliance
  • Conduct a Company-Wide Gap Analysis and Internal Audit
  • Ensure Your Contractors Are Ready for Compliance
  • Educate Key Stakeholders on Data Governance
  • Understand an Auditor’s Perspective
  • Safeguard Data and Information
  • Effectively Use CAPA When Things Go Wrong
  • Implement Strategies for Audit Trials, Data Migration and
    Part 11 Compliance

28-30 March 2017 DoubleTree Centraal Station Amsterdam