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USA | Reagan-Udall Foundation Meeting Summary Highlights Real-World Data Challenges for At-Home Diagnostics

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USA | Reagan-Udall Foundation Meeting Summary Highlights Real-World Data Challenges for At-Home Diagnostics2026-08-10T17:32:46+00:00

UK | MHRA Sets Out Data Needs for Regulatory Decision-Making — HDRS Seen as Opportunity to Improve Regulatory Access to RWD

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UK | MHRA Sets Out Data Needs for Regulatory Decision-Making — HDRS Seen as Opportunity to Improve Regulatory Access to RWD2026-08-10T17:25:30+00:00

GREECE | Ministerial Decisions Update Clinical Research Site Rules and Digital Safety Communications — Limited but Relevant Signals for RWR

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GREECE | Ministerial Decisions Update Clinical Research Site Rules and Digital Safety Communications — Limited but Relevant Signals for RWR2026-08-10T17:19:14+00:00

GERMANY | Federal Cabinet Approves GeDIG — Draft Law Sets Out National EHDS Secondary-Use Framework

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GERMANY | Federal Cabinet Approves GeDIG — Draft Law Sets Out National EHDS Secondary-Use Framework2026-08-10T17:15:26+00:00

EU | Pharmaceutical Reform Enters Legal-Linguistic Finalisation — EMA Establishes Implementation Governance and Begins Stakeholder Engagement

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EU | Pharmaceutical Reform Enters Legal-Linguistic Finalisation — EMA Establishes Implementation Governance and Begins Stakeholder Engagement2026-08-10T17:10:48+00:00

EU | HTACG Sets AI Transparency Expectations for JCA Dossiers — Human Oversight, Tool Disclosure and Prompt Records Required

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EU | HTACG Sets AI Transparency Expectations for JCA Dossiers — Human Oversight, Tool Disclosure and Prompt Records Required2026-08-10T17:01:33+00:00

EU | EMA Steps Up Women’s Health Initiative — Evidence Gaps, Pregnancy Data and RWE Move Higher on the Regulatory Agenda

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EU | EMA Steps Up Women’s Health Initiative — Evidence Gaps, Pregnancy Data and RWE Move Higher on the Regulatory Agenda2026-08-10T16:57:00+00:00

EU | Two Joint Clinical Assessments Discontinued After Dossiers Fail HTAR Requirements — Evidence Completeness, PICO Coverage and Reproducibility Become Critical

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EU | Two Joint Clinical Assessments Discontinued After Dossiers Fail HTAR Requirements — Evidence Completeness, PICO Coverage and Reproducibility Become Critical2026-08-10T16:49:59+00:00

BRAZIL | INAEP Opens CEP Accreditation Process — High-Risk Research Review Moves Further Into Operational Implementation

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BRAZIL | INAEP Opens CEP Accreditation Process — High-Risk Research Review Moves Further Into Operational Implementation2026-08-10T16:48:14+00:00

USA | FDA Reissues Draft Guidance on Substantial Evidence of Effectiveness — Non-Interventional Studies Expressly Recognised Within the Adequate and Well-Controlled Investigation Framework

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USA | FDA Reissues Draft Guidance on Substantial Evidence of Effectiveness — Non-Interventional Studies Expressly Recognised Within the Adequate and Well-Controlled Investigation Framework2026-08-10T16:40:04+00:00
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