GRS

TRANSLATE

MENU menu

Close close menu

GRS Blog

PAST POSTS menu

Close close menu

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)

 

 

Past Posts...

Stem Cells and Autism
18 September 2011