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Resource Type: MRCT Sponsor Resource
Data Use Agreement Word Document
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Informed Consent Form Word Template – External Sponsor
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Informed Consent Form Word Template – No External Sponsor
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ICH E17 Scientific and Regulatory Workshop Slides
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India: Progress and Opportunities
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Regulation of New Drugs and Clinical Trials Rules: Comments and Recommendations
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Guiding Principles for Clinical Trials 2017
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Introduction to Return of Individual Results Group
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MRCT Center 2016 Annual Meeting Slides
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