The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is unique. It brings together regulatory authorities and the pharmaceutical industry to discuss scientific and technical aspects of drug registration.
In Jan 2025, the International Council for Harmonisation (ICH) endorsed the latest revision of the ICH Guideline for conducting clinical trials titled “ICH E6(R3) Guideline for Good Clinical Practice.
The ICH GCP guidelines set out the requirements for:
- protocol amendments
- trial documentation
- indemnity
- reporting lines for adverse events
- provision of medical care for trial participants.
Training & Development
ICH Good Clinical Practice course (available in multiple languages)
The ICH Good Clinical Practice (GCP) E6 training is a structured educational program. It aims to familiarise clinical research professionals with the ethical standards in the ICH E6 guideline. It also covers the scientific quality standards. This training ensures that individuals involved in clinical trials understand and adhere to practices that protect participant rights. It ensures data integrity. It also ensures compliance with regulatory requirements.
Resource
Nursing Education Network 
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