Good Clinical Practice and ICH GCP Guidelines

What everybody should know about Clinical Trials!
Without clinical trials, we wouldn’t have any vaccines, treatments for cancer, heart disease, diabetes and many others. What should everybody know about Clinical Trials? How are pharmaceuticals and medical devices developed? This is our new video of our series about the basics of clinical trials to give you some answers. "Good Clinical Practice and ICH GCP Guidelines" is presented by our expert and Carol Lazovic.

For more insight into our world of Clinical Research, and to be sure not to miss a thing,

It’s all about the mindset, the GCP-Mindset 💡

[PO-cxej]

For anyone who is curious, the 13 principles of the ICH GCP are the following:
Ethics
 Trial risk vs trial benefit
 Trial participants
 Information on the Medicinal Product
 Good quality trials
 Compliance with the study protocol
 Medical decisions
 Trial staff
 Informed consent
 Clinical trial data
 Confidentiality
 Good Manufacturing Practice
 Quality assurance

[raunakmukherjee]

Does GCP applies to clinical feild in animal testing phase?

[mohammadyounis]

Do you have online courses for gcp that gives an international certificate..

[DikshaSharma-qbes]

Mam how we camlare inform consent form requirements ; compare ICH guidelines with germany

[minigashailaja]

Hi mam iam shailaja I completed my m pharmacy and I completed training on pv and CDm j need job opportunity plz help me mam