by GCP Central | Jan 29, 2024 | GCP Central News
We are getting more and more questions about the EU CTR. The transition period is about to end, and we ‘re noticing it. That’s why we would like to share with you the most critical issues: The Clinical Trials Regulation (Regulation (EU) No 536/2014) or, in short, the...
by GCP Central | Dec 20, 2023 | GCP Central News
The Nederlandse federatie van umc’s (NFU) (English: Dutch Federation of University Medical Centers) has awarded GCP Central the contract to develop further and maintain the e BROK® course from 2024 to 2027. The BROK® (Basiscursus Regelgeving en Organisatie voor...
by GCP Central | Nov 30, 2023 | GCP Central News
GCP Central has now been in existence for more than ten years. It is a time in which we have put all our energy, passion, and dedication into training the international community of scientific researchers on good clinical practice, or GCP, and locally applicable laws...
by GCP Central | Oct 29, 2023 | GCP Central Products
The upcoming update to ICH GCP (R3) sees vital guideline changes with layout changes and additional sections. There are also additions, incorporating new topics such as remote access, digital consent, decentralized clinical trials, reporting, and record...
by GCP Central | Aug 22, 2023 | updates law & regulations
What is coming with ICH GCP R3? Since ICH GCP (or officially, ICH E6 R1) was first drafted more than 20 years ago, the complexity of clinical trials has increased, with the design of trials, technology use, and data quality and collection changing to the evolving face...
by GCP Central | Jul 24, 2023 | GCP Central News
GCP Central has been around for more than ten years. A time when we have put all our energy, passion and dedication into training the international community of medical scientific researchers in the field of good clinical practice, or GCP. So that scientific research...
