Considerations for Compliance with the EU General Data Protection Regulation (GDPR)

The General Data Protection Regulation (GDPR) establishes a legal framework that sets guidelines for the collection and processing of personal information from individuals residing in the European Union (EU). GDPR compliance is a challenge for life science companies and services providers alike. Understanding and implementing compliance obligations under the GDPR is an ongoing process that requires review and assessment as companies grow and expand to include new business opportunities, implement new systems and/or establish new practices and processes. Companies must continue to ensure compliance with privacy standards that meet or exceed the demands of the highly technical digital world that we live in.

In this white paper, Larry Davis provides a thorough understanding of the GDPR, including all of its key compliance provisions and terminology, then outlines the fundamental obligations for GDPR compliance.

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“Considerations for Compliance with the EU General Data Protection Regulation (GDPR)”
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Author
Larry Davis, PharmD
Vice President, Medical and Clinical Affairs

Larry is a pharmaceutical and biotech industry professional with over 20 years of experience in the areas of medical and clinical affairs and drug safety pharmacovigilance, as well as in quality and regulatory compliance. He has a proven record of accomplishment in building and leading high-performing teams including those for office and field-based medical affairs […]