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UK Conditions and ICH-GCP R3 Principles of GCP V1.0
UK Conditions and ICH-GCP R3 Principles of GCP V1.0
Published 21/01/2026 |PDF, 130 KB
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Plain English glossary of clinical trial terms V1.0
Plain English glossary of clinical trial terms V1.0
Published 21/01/2026 |PDF, 203 KB
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Effective from 28 Apr 2026: SOP 20. Lab: Sample Management in Clinical Trials
Effective from 28 Apr 2026: SOP 20. Lab: Sample Management in Clinical Trials
Published 05/01/2026 |PDF, 348 KB
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Effective from 28 Apr 2026: SOP 12. Application and Maintenance of a Clinical Trial Authorisation (CTA)
Effective from 28 Apr 2026: SOP 12. Application and Maintenance of a Clinical Trial Authorisation (CTA)
Published 05/01/2026 |PDF, 494 KB
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Effective from 28 Apr 2026: SOP 7. Obtaining Informed Consent for Clinical Trials
Effective from 28 Apr 2026: SOP 7. Obtaining Informed Consent for Clinical Trials
Published 05/01/2026 |PDF, 459 KB
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Effective from 28 Apr 2026: SOP 6. Notification of a Serious Breach
Effective from 28 Apr 2026: SOP 6. Notification of a Serious Breach
Published 05/01/2026 |PDF, 377 KB
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Effective from 28 Apr 2026: Pharmacovigilance and Safety Reporting Policy
Effective from 28 Apr 2026: Pharmacovigilance and Safety Reporting Policy
Published 05/01/2026 |PDF, 379 KB
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ICH GCP E6 (R3) and the updated UK clinical trials regulations
What we know so far about changes to clinical regulations taking effect on 28 April 2026.
Published 24/09/2025 |DOCX, 220 KB
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