Share 'Compliance with the New ICH GCP Revision 2 Addendum'
Overview:This will enable you to meet the new international GCP standard to ensure regulatory compliance and the acceptance of clinical trial data by the regulatory authorities internationally.
Why should you Attend:With the new ICH GCP E6 Revision 2 Addendum now finalised the changes should have been implemented for organisations running clinical trials.
Areas Covered in the Session:Review the n…
You can share this event in two ways…
Share this link:
Send it with your computer's email program: Email this