by GCP Central | Feb 23, 2026 | updates law & regulations
The EU AI Act is no longer a proposal. It is law, and it applies in stages. The European Commission sets out the application timeline, including key dates in 2025 and 2026, with some obligations running on longer transition periods into 2027. The staged timeline is...
by GCP Central | Jan 30, 2026 | GCP Central News
ICH E6(R3) has moved from guideline text to regulatory expectation across Europe. At the same time, trial delivery is becoming more platform-driven, more vendor-distributed, and increasingly supported by AI-enabled functions inside those systems. Monitoring...
by GCP Central | Nov 26, 2025 | GCP Central News
If you are registered in the Dutch GCP-WMO register, you know your certification is time-limited. Three years after you pass the GCP exam, your registration expires, and you need recognized re-certification training to stay on the register. At the same time, finding a...
by GCP Central | Mar 5, 2025 | GCP Central News, GCP Central Products
The ICH Good Clinical Practice (GCP) guideline has been updated, and the transition from version R2 to R3 brings significant changes for clinical research professionals. To help you stay compliant and implement these updates effectively, GCP Central has launched the...
by GCP Central | Jan 21, 2025 | GCP Central News
GCP Central is pleased to welcome Femke Kuiper as our newest Business Development Manager. With over 20 years of experience in the pharmaceutical, medical device, and animal health industries, she brings a wealth of expertise in sales, marketing, and project...
by GCP Central | Jan 21, 2025 | GCP Central News
The International Council for Harmonisation (ICH) is making critical updates to its Good Clinical Practice (GCP) guidelines under Revision 3 (R3). These changes aim to modernize clinical trial practices and adapt to the evolving needs of research. Here’s a detailed...
