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Pharmaceutical Data Integrity - Webinar

  • ID: 4899669
  • Webinar
  • November 2019
  • Region: Global
  • 90 Minutes
  • Compliance Online
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Why Should You Attend:

In their guidance on data integrity, all regulators emphasize a risk-based approach to ensure that effort is focused on the greatest risks. This approach should help companies to achieve compliance with regulators’ expectations without committing a disproportionate amount of human or financial resource. This webinar will explain to attendees why data integrity is so important and spell out some of the common honest mistakes that could lead to regulatory enforcement action. The risk-based approach recommended by regulators is also explained in detail.

Areas Covered in the Webinar:

Data integrity myths
Historical background
Definition of data integrity
Current regulatory approach
Guidance
Static and dynamic records
Non-conformance trends
Example enforcement letters
Data integrity risks in the analytical process
Conducting a data integrity risk assessment
Common causes of data integrity breaches
Practical tips on achieving compliance
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Dr Mark Powell is a Fellow of the Royal Society of Chemistry (RSC) with over thirty years’ experience as an analytical chemist. Mark was Honorary Treasurer of the RSC’s Analytical Division and led a working group on continuing professional development until July 2016, when his term of office ended. Between 2003 and 2013, he was the Analytical Development Manager, and later Scientific Manager, of a UK-based contract research organization which specialized in early-stage oral drug development. In 2013, he set up Mark Powell Scientific Limited, which provides training and consultancy services to pharmaceutical companies. Mark has since enjoyed working with companies of all sizes around the world on a variety of training and consultancy assignments.
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