Investigative Site Staff
"the investigator should be aware of, and should comply with, GCP and the applicable regulatory requirements." ICH-GCP E6(R2) - 4.1.3
AGCP offers 'GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus)' toInvestigative Site Staff, meeting TransCelerates mutual recognition program requirements.
Preparing and Conducting Regulatory Inspections
AGCP presents an online course for Investigative Sites and Sponsors to learn from experiencedindustry professionals sharing their knowledge and experience from regulatory inspections.
The Academy of Good Clinical Practice (AGCP) is a 501(c)(3) registered non-profit organization which focuses on the professional development of individuals working within Clinical Development arena. AGCP provides a robust and established platform for seasoned subject matter experts and industry leaders to share their knowledge and experiences, with those who are either new to the industry, those who seek to develop within their current roles, or those who simply wish to develop new skills, knowledge, expertise and meet industry professionals with similar goals, objectives and interests.