Clinical Research Training for Investigators

Kursinhalte
Investigators are trainer on their specific duties within Clinical Research. In 1 day, they get to understand the regulations, GCP guidelines and their responisbilities with regards to safety reporting and informed consent. Participants will receive a GCP certificate showing their capacity to work according to the current laws and regulations.

Lernziele, Trainingsziele
To know everything about current clinical practice
To understand the responsabilities of a Medical Doctor withing Clinical Trials
To fully comprehend the safety reporting procedure
To be able to get a voluntary and understandable informed consent

Zielpublikum
Medical Doctors looking to participate in Clinical Trials. Investigators conducting Clinical Research.

Zertifizierung
ISO 9001:2008 / Q-for

Lokaler Veranstalter
European Centre for Clinical Research Training

Frau Sunita Kelecom