How to Gain Authorisation for Clinical Research under the EU Clinical Trials Regulation

Online Course • grapl

About the CPD course

To conduct a clinical trial in one or more member states of the European Economic Area (EEA) a sponsor must first gain the approval of each relevant national regulator and the favourable opinion of research ethics committees relevant to the investigational sites. The European Union Clinical Trials Regulation ensures that the rules for assessing clinical trial applications and for conducting trials are identical throughout the EEA. Sponsors of all new such trials must now comply with the Regulation. This course sets out the procedures that sponsors need to follow to gain authorisation to conduct clinical trials under the Regulation.

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grapl

grapl is a UK based digital learning and development specialist, authoring and designing Zenosis® courses to provide an extensive eLearning library for the pharmaceutical, biotech and medicinal products sector. This learning can be delivered via the customers LMS, the grapl LMS or its social, knowledge and collaborative CloudRooms platform. Continuously updated to reflect regulatory changes, Zenosis® courses are trusted to educate their people by some of the worlds leading companies.