The EU Clinical Trials Register currently displays 43881 clinical trials with a EudraCT protocol, of which 7295 are clinical trials conducted with subjects less ...
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People also ask
Is Directive 2001/20 EC still valid?
On 31 January 2022, the Regulation repealed the Clinical Trials Directive (EC) No. 2001/20/EC and national implementing legislation in the EU Member States, which regulated clinical trials in the EU until the Regulation's entry into application.
What kinds of trials require an EudraCT number?
A EudraCT number is required in order to apply to the Medicines and Healthcare products Regulatory Agency (MHRA) for a Clinical Trial Authorisation (CTA) and to apply for REC approval of your clinical trial.
Which countries are involved in the EU CTR?
The EUCTR replaces the previous European Clinical Trials Directive and governs the conduct of clinical trials in all EU Member States, including Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, ...
What is the NCT number in clinical trials?
NCT Number: The National Clinical Trial number is an identification that ClinicalTrials.gov assigns a study when it is registered. The NCT number is in the format “NCTXXXXXXXX”. Until an NCT number is assigned, the study is not registered.
The EU Clinical Trials Register provides a free and accurate search of clinical trials in European Union member states and the European Economic Area.
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Volume 10 of the publication "The rules governing medicinal products in the European Union" contains guidance documents applying to clinical trials.A…
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Clinical trial search. Search Criteria. Search results. Display options. Basic Criteria. Contain all of these terms: Contain any of these terms:.
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Jan 12, 2024 · In 2011, the European Union Clinical Trials Register (EUCTR) launched providing a public facing, searchable registry that covered most trials in ...
The Clinical Trials Regulation is set to replace the Clinical Trials Directive once it comes into application.Although the Regulation entered into…
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This website, maintained by EMA, provides information on clinical trials in the EU and is underpinned by the Clinical Trials Information system.
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Feb 11, 2022 · Using data scraped from the full European Union Clinical Trials Register public dataset, we examined the extent of issues with three areas of ...
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