2016 ISPE Data Integrity Workshop

Learn hands-on approaches for identifying, mitigating, and remediating potential causes of breaches in data integrity by participating in the ISPE Data Integrity Workshop on 5 June 2016 in Bethesda, MD.

Held in conjunction with the 2016 ISPE/FDA/PQRI Quality Manufacturing Conference*, this special half-day event will identify important regulatory issues impacting data integrity and help answer key questions surrounding current expectations. You will take part in:

  • Hypothetical Scenarios and Simulated Fact Pattern Group Sessions
  • Reviewing Regulatory Actions and Key Contributors to Data Integrity Issues
  • Learning Industry Best Practices and Mitigation Strategies

This interactive workshop is the ideal place to discuss the current data integrity environment with your colleagues and explore solutions from industry and regulatory leaders. For more information, please visit our website.

*Register for both the ISPE Data Integrity Workshop and the ISPE/FDA/PQRI Quality Manufacturing Conference and save $100!


Data integrity is THE question facing regulatory agencies and the pharmaceutical industry.

Patients need to trust that the drugs they take have been manufactured according to strict regulation and oversight, that the drugs they put into their bodies are of the highest quality, that all pharmaceutical companies, regardless of geography, have embraced a culture of compliance.

Pharmaceutical Engineering® magazine’s six-part special report on data integrity explores this multifaceted subject in detail, describing the desired state, identifying red flags, and enumerating best practices. Our experts define the strategies that drive prevention, detection, and response.

View the special report on data integrity today from Pharmaceutical Engineering® magazine with your ISPE membership.  Not an ISPE Member?  Join today to review the 28-page report containing insight you won’t get anywhere else.

 

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