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Track 1: Clinical Safety and Pharmacovigilance

DIA 2017: Driving Insights to Action

This track provides an overview of the global regulatory environment in the field of clinical safety and pharmacovigilance for medical products (biopharmaceutical products, advanced therapies and medical devices), with a focus on pragmatic approaches to protecting patient safety and incorporating the patient voice into the complex and evolving pharmacovigilance ecosystem. Forward-thinking sessions address the application of new technologies and methods to streamline pharmacovigilance systems and processes to enhance protection of patient safety as products become more complex, new data sources drive new analytical techniques, regulatory requirements become more detailed, and medical product development becomes more global.

Sessions in Clinical Safety and Pharmacovigilance

Sunday, June 14 | Short Courses

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Monday, June 15

Tuesday, June 16

Wednesday, June 17

On Demand

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