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Training on Current ICH GCP Guidelines 2013
06 Feb 2013
Webinar
Home
Training on Current ICH GCP Guidelines 2013
Key Topics
Coverage of ICH requirements for the Investigator, the sponsor and IRBs
Background information on the need for standardized GCP guidelines for the clinical research industry
Subject rights
Informed consent
What is an essential document?
What is an adverse event?
Retention requirements
Who should Attend
Research Nurses
Principal Investigators
CRAs
Study Coordinators
Healthcare professionals needing to acquire documentation of current ICH GCP training
Quality Assurance
Read more
Past Events
Training on Current ICH GCP Guidelines 2013 - 06 Feb 2013, Webinar
(36535)
Training on Current ICH GCP Guidelines 2026
Important
Please, check "Training on Current ICH GCP Guidelines" official website for possible changes, before making any traveling arrangements
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Education:
Training
Health & Medicine:
Healthcare, Medical device, Medical laboratories, Medical technology, Pharma
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