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Track 8: R&D Quality and Compliance

DIA 2017: Driving Insights to Action

This track provides a comprehensive view of the quality landscape across the preclinical, clinical, and pharmacovigilance domains within the biopharmaceutical industry. Sessions are focused on discussing innovative and risk-proportionate approaches to managing quality that are appropriate to an evolving development paradigm and in a global context. Sessions will address key topics in GLP, GCP, and PV quality, providing knowledge and resources needed to implement pragmatic, proactive, and effective quality management.

Sessions in R&D Quality and Compliance

Monday, June 21-Friday, June 25 | Short Courses

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Monday, June 28

Tuesday, June 29

Wednesday, June 30

Thursday, July 1

Who is This Track Designed For?

Professionals involved in: Research and development, clinical research, clinical, preclinical, or PV quality, clinical monitoring, regulatory affairs, regulatory operations, compliance, pharmacovigilance, quality control/quality assurance, and clinical quality management systems.

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