Clinical trials for medicines: apply for authorisation in the …
https://www.gov.uk/guidance/clinical-trials-for-medicines-apply-for-authorisation-in-the-uk
When A Clinical Trial Authorisation (CTA) Is NeededTrial Sponsor and Legal RepresentativeRegistration of Your Clinical TrialCombined Review of Clinical Trials of Investigational Medicinal ProductsIn Vitro Diagnostic Medical DevicesDocuments to Send with Your ApplicationAssessment of Your SubmissionCommon Issues Identified During Clinical Trial ApplicationsWithdraw Your Request Before The Final DecisionRisk Proportionate ApproachesFrom 1 January 2022, all new Clinical Trials of Investigational Medicinal Products (CTIMPs) applications will be prepared, submitted and reviewed via the combined review service. This offers CTIMP applicants and sponsors a single application route and co-ordinated review by MHRA and the research ethics committee, leading to a single UK decision. Ap...See more on gov.uk From 1 January 2022, all new Clinical Trials of Investigational Medicinal Products (CTIMPs) applications will be prepared, submitted and reviewed via the combined review service. This offers CTIMP applicants and sponsors a single application route and co-ordinated review by MHRA and the research ethics committee, leading to a single UK decision. Ap...
From 1 January 2022, all new Clinical Trials of Investigational Medicinal Products (CTIMPs) applications will be prepared, submitted and reviewed via the combined review service. This offers CTIMP applicants and sponsors a single application route and co-ordinated review by MHRA and the research ethics committee, leading to a single UK decision. Ap...
DA: 21 PA: 80 MOZ Rank: 29