Presentations from the IMB’s Clinical Trials Seminar for Medicinal Practitioner Sponsors and Investigators

This June the Irish Medicines Board (IMB) hosted its Clinical Trials Seminar for Medicinal Practitioner Sponsors and Investigators. The event discussed the clinical trial application process, regulatory practices, sponsor/investigator responsibilities and safety measures.

Out of this came several presentations which may be useful to those in the clinical research industry. They can be found, courtesy of the IMB’s website, at the following links:

Good Clinical Practice Inspections Expectations for Compliance with Sponsor Responsibilities, Part I

Good Clinical Practice Inspections Expectations for Compliance with Sponsor Responsibilities, Part II

Life Cycle of the Clinical Trial 

Clinical Trials – Applications Process, Legislation & Guidelines 

Overview of Adverse Reaction Reporting Requirements in Clinical Trials