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Save the date! EU Clinical Trial Regulation New Legal Framework for Multi center Clinical Trials Friday, December 16, 2016, WWF Auditorium University of Basel, Law Faculty, Peter Marianne 8, CH4002
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What is eu clinical trial regulation?
The EU Clinical Trial Regulation is a set of rules and guidelines that govern the conduct of clinical trials in the European Union.
Who is required to file eu clinical trial regulation?
Any organization or individual conducting a clinical trial in the EU is required to file the EU Clinical Trial Regulation.
How to fill out eu clinical trial regulation?
To fill out the EU Clinical Trial Regulation, organizations and individuals must provide detailed information about the study design, participant eligibility criteria, and safety monitoring procedures.
What is the purpose of eu clinical trial regulation?
The purpose of the EU Clinical Trial Regulation is to ensure the safety and efficacy of clinical trials conducted in the EU, and to streamline the regulatory process for researchers.
What information must be reported on eu clinical trial regulation?
The EU Clinical Trial Regulation requires information on the study protocol, informed consent process, adverse event reporting procedures, and study results to be reported.
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