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FDA’s 2011 Draft Guidance on Financial Disclosure by Clinical Investigators – Overview of Recommendations
Trending Compliance Trainings

Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
By - Rachelle D Souza
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By - Rachelle D Souza
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Trial Master File and Clinical Data Management Regulated by FDA
By - Carolyn Troiano
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By - Carolyn Troiano
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Annual Current Good Manufacturing Practices (cGMP) Training
By - Kelly Thomas
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By - Kelly Thomas
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Issues related to informed consent in clinical trials
By - Sarah Fowler Dixon
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By - Sarah Fowler Dixon
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