Ireland: Guide to Clinical Trial Applications
09/1/2012
The Irish Medicines Board (IMB) has released new guidance to applicants in making applications for clinical trials on medicinal products for human use to the IMB as competent authority for these Regulations.
Guidance on applications to ethics committees is available on the website of the Department of Health. Information on clinical trials using medicinal products containing genetically-modified organisms is available from the Environmental Protection Agency (www.epa.ie).
Author: Greer Deal, Director of Global Regulatory Services (GRS)