Guide to Clinical Trial Applications
14 January 2013
The document below is intended to give guidance to applicants in making applications for clinical trials on medicinal products for human use to the Irish Medicines Board (IMB) as competent authority for these Regulations. Guidance on applications to ethics committees is available on the website of the Department of Health (www.dohc.ie). Information on clinical trials using medicinal products containing genetically-modified organisms is available from the Environmental Protection Agency (www.epa.ie).
To read the guide, click on the link below:
Guide to Clinical Trial Applications
To see the most recent changes to this guide, click on the link below:
Guide to Clinical Trial Applications - changes tracked