In the ever-evolving landscape of clinical research, staying up to date with regulatory standards is crucial. The International Council for...
Understanding the Differences Between ICH GCP E6 R2 and R3: Why Compliance and Training Matter
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Understanding ICH GCP E6 (R3) Annex 2
The next phase of the ICH GCP E6 (R3) modernisation is on its way, and Annex 2 is set to reshape how sponsors, CROs and investigators approach...
Why Do I Need to Renew My GCP Certificate in R3 Before the Implementation Deadline?
If you work in clinical research, you’ve likely heard that good clinical practice (GCP) has undergone a significant revision. The latest update –...
Good Clinical Practice E6 (R3) Guidance and Implementation
Understanding the Updated ICH GCP E6 (R3) Guidance Good Clinical Practice (GCP) is the internationally recognised standard for designing,...
Why is informed consent crucial in clinical trials?
Just imagine being presented with an opportunity to participate in a clinical trial without knowing the potential side effects, the purpose of the...
How To Become A Clinical Research Project Manager
To become a clinical research project manager, you will need a combination of education, experience, and specific skills. There isn’t one specific...