JANUARY 15, 2010

Good Clinical Practice (GCP) for Investigators and other Research Personnel


Reviewed and Approved by IPULS

Description
History of GCP
Declaration of Helsinki
Pronciples of GCP
Ethics Committee
Investigator's responsibilities
Sponsor's responsibilities
Safety reporting (AE, SAE, SUSAR)
Informed Consent
Protocol and Amendments
Investigator's Brochure
Essential documents

Target Group
Investigators and other research personnel working with clinical trials.

When?
Whenever it suits you!

Where?
In your premises or other relevant location agreed upon.

Please contact us for further information and cost proposal!

News
 
JULY 7, 2010
TFS Academy moves into CEE, with courses to run in Warsaw, Prague and Budapest this Autumn

JULY 7, 2010
New courses for Autumn 2010 - Presentation Skills, Clinical Trials in the Paediatric Population