BRAZIL | Major Reform of the National Human Research Ethics System
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UK | Changes to REC Annual Progress Report Requirements
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EU | MDCG Guidance on Content of Clinical Investigation Plans for Medical Devices
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EU | Launch of New HMA-EMA Catalogues of Real-World Data Sources and Studies
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USA | New Draft FDA Guidance: Collection of Race and Ethnicity Data in Clinical Trials and Clinical Studies for FDA-Regulated Medical Products
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GLOBAL | 2024 Revision of the Declaration of Helsinki
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USA | FDA Finalises Guidance on “Data Standards for Drug and Biological Product Submissions Containing Real-World Data
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UK | Updates to Commercial Model Agreements
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UK | Removal of the Commercial Standalone Data Processing Agreements
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