FINLAND | National Cybersecurity Act 124/2025 Transforms Drug and Device Research Operations
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EU | Impact of the NIS 2 Directive on Pharmaceutical Companies Conducting Research and Development
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EU | Updates From Latest EMA Report on Regulator-Led Studies Using RWD
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EU | New Pharmaceutical Legislation Moves Closer to Implementation
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UK | New Amendment History Log Template
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EU | Proposed Amendments to Regulation EU/520/2012 Affecting Post-Authorisation Safety Studies
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- UK | MHRA Releases Draft Guidance on Using Real-World Data for External Control Arms in Clinical Trials Gallery
UK | MHRA Releases Draft Guidance on Using Real-World Data for External Control Arms in Clinical Trials
2025, May 2025, Members-Only, Minor Update, RWD to Support Reg Decisions, Secondary Use of Existing Data, UK
UK | MHRA Releases Draft Guidance on Using Real-World Data for External Control Arms in Clinical Trials
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GLOBAL | New CIOMS report: Benefit-Risk Balance for Medicinal Products
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GERMANY | Proposed Centralisation of Data Protection Supervision
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