European Medicines Agency (EMA) updated GCP draft published for comments
Posted onAn update as an addendum to the ICH GCP E6 has been released by European Medicines Agency (EMA) for comments from the public.
An update as an addendum to the ICH GCP E6 has been released by European Medicines Agency (EMA) for comments from the public.
Good Clinical Practice (GCP) is a well accepted global scientific quality and moral standard for performing clinical studies that engage human volunteers. ICH-GCP certification is mandatory for any professional who try to associate with clinical research anywhere around the Globe. This is making GCP training a compulsion to participate or carve a career in this […]
GCP (Good Clinical Practice) is a world wide technical quality and ethical custom for planning, performing, gathering and reporting of clinical research outcomes in the form of data that engross human volunteers.
Good Clinical Practice (GCP) Certification :- Good Clinical Practice (GCP) is a global scientific quality and ethical standard for scheming, conducting, collecting and reporting of clinical study data that engage human subjects.
Good Clinical Practice is intended to be a global ethical and scientific quality standard for designing, conducting, monitoring, recording, auditing, analyzing and reporting bio medical and behavioral research studies involving human participants. The history of Good Clinical Practice (GCP) statute traces back to one of the oldest lasting practices in the history of medicine: The Hippocratic Oath. As […]