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Clarity on Clinical Investigations: What You Need to Know About EU-MDR and ISO/DIS 14155:2018

Thursday, Sept. 19, 2019 • 1:30 p.m. - 3:00 p.m. EDT
The world of clinical investigations is changing rapidly, with the EU-MDR’s new and more complex system and the forthcoming ISO/DIS 14155:2018 updates. Noted expert Dan O’Leary, President of Ombu Enterprises, LLC, will explain these requirements and concepts in a comprehensive, easy-to-understand approach.

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CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, market research, benchmark reports and information services used by all industry professionals involved in the management and conduct of clinical trials.

Top Headlines

Drugmakers Support FDA’s Expanded Trial Eligibility Plan, GAO Says

Ask the Expert: Protocol Deviations and Publishing Case Studies

Biogen and Eisai End Three More Alzheimer’s Studies


Download detailed articles investigating and analyzing current trends in the clinical trials industry and the impact they have on the research community.