DIA 2017 Annual Meeting has ended

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DIA 2017 Annual Meeting

11:00am CDT

#109: Submission Dossiers: Communications Excellence to Drive Speed and Quality S503ab #110: Globalization of Medical Affairs Departments S504abc #112: Data Sharing: 2017 and Beyond N426b #118: Counting on Safety S401d #119: Designing and Implementing a Robust Pharmacovigilance System for Vaccines S401bc #127: The Evolving International Landscape of FDA Inspections: Data Integrity Violations in Bioequivalence Studies in India S405a

10:30am CDT

#214: Recent Trends in Asian Regulations for Drug Development: What is Coming Next? N227b #216: International Collaboration in Times of Public Health Crisis N229

2:00pm CDT

#252: What’s New in Devices: European Medical Device Regulations and MDUFA IV S404a #254: New Considerations in Benefit-Risk Management S403ab

4:00pm CDT

#278: PMDA Town Hall S404a

10:30am CDT

#320: The Brave New World: The Ongoing Globalization of Pharmacovigilance N226 #327: Multiregional Clinical Trials and the ICH E17 S402ab

2:00pm CDT

#341: EMA Policy 0070: A Game Changer for Industry N227b #345: Global Perspective on ICH: Part 1 of 2 N228

4:00pm CDT

#373: FDA–Health Canada Regulatory Cooperation Council Town Hall S401d #367: Writing of Layperson Summaries of Clinical Trial Results According to the EU: Regulation and Its Impact on Global Pharmaceutical Activities S502ab #371: Global and Regional Collaboration Initiatives: Challenges, Opportunities, and Case Studies S403ab #374: Global Perspective on ICH: Part 2 of 2 N228 #376: Changing Environments Within Pharmacovigilance S404d #378: Looking to the Future for EU Pediatric Investigation Plans S501abc

10:45am CDT

#403: Driving International Awareness and Use of Regulatory Writing Guidelines: Case Studies of the Clarity and Openness in Reporting (CORE) Reference Guidelines S403ab