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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- EU | EMA Catalogues of Data Sources and Non-Interventional Studies Go Live in February 2024 Gallery
EU | EMA Catalogues of Data Sources and Non-Interventional Studies Go Live in February 2024
December 2023, EU, Members-Only, RWD to Support Reg Decisions, Secondary Use of Existing Data, Significant Update
EU | EMA Catalogues of Data Sources and Non-Interventional Studies Go Live in February 2024
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EU | Data Quality Framework for EU Medicine Regulation Finalised
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LATVIA | New Medical Device Regulations
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