ICH GCP E6(R3) is about to go live in the EU

June 24, 2025

ICH GCP E6(R3) is about to go live in the EU

The countdown is on – ICH GCP E6(R3) is about to go live in the EU, and everyone’s getting prepared!

As a service provider (you caught that new R3 definition during training, right?), Flex Databases is here to support you through the transition. Let’s highlight a few areas that are especially important for our clients:

✅3.6.8 The sponsor should have access to relevant information (e.g., SOPs and performance metrics) for selection and oversight of service providers.
We’re always audit-ready. From SOPs and organizational charts to system documentation – everything you need for a smooth, effortless vendor assessment is at your fingertips.

✅3.6.9 The sponsor should ensure appropriate oversight of important trial-related activities that are transferred to service providers, including activities further subcontracted by the service provider.
We’ve got you covered with uptime reports, backup logs, and testing records – transparent and traceable metrics to support robust oversight, no surprises.

✅3.9.5 The range and extent of oversight measures should be fit for purpose and tailored to the complexity of and risks associated with the trial. The selection and oversight of investigators and service providers are fundamental features of the oversight process. Oversight by the sponsor includes quality assurance and quality control processes relating to the trial-related activities of investigators and service providers.

Let’s simplify this together. A Quality Agreement helps capture all expectations clearly – so you stay in control without wasting time or resources.

Have questions or want to start your oversight planning? We’re just a message away. 👉 contact@flexdatabases.com

Blog

July 22, 2025
Electronic Data Capture – Everything You Need To Know

What is Electronic Data Capture? Electronic Data Capture (EDC) is an electronic system applied to clinical trials for capturing, managing, and storing patient data. Instead of paper-based forms, investigators enter clinical trial information directly into a secure, web-based site. EDC systems validate data integrity, reduce errors, and automate the data collection process – accelerating clinical […]

Data Hosting with Confidence – Flex SaaS for Clinical Trial Environments 

At Flex Databases, we deliver a SaaS solution purpose-built for clinical trials – offering global accessibility with full transparency and control over where your data resides.  Not a Public Cloud. A Dedicated SaaS Platform You Can Trust.  Flex Databases is an EU-based company operating globally and trusted by life sciences organizations for secure, validated SaaS […]

July 14, 2025
What is CTMS? Frequently Asked Questions

What is CTMS A CTMS – Clinical Trial Management System is a software solution that facilitates more streamlined management and monitoring of clinical trials. Clinical operations teams like project managers, CRAs, and study coordinators in pharmaceutical firms, CROs, and biotech firms use the tool to oversee everything from site selection and subject recruitment to monitoring […]

July 3, 2025
Everest CRO Experience with Flex Databases

Dana Leff Niedzielska, MBA, SVP of Global Clinical Operations at Everest Clinical Research, shares her experience using Flex Databases’ CTMS and eTMF. In this interview, Dana highlights how Flex Databases supports Everest CRO’s clinical operations. Learn why Everest chose Flex Databases as their trusted technology partner and why they continue to rely on and trust […]

Contact us

Get in touch to discuss compliance, implementation, demos, pricing

We are here for all of your questions! Tell us more about yourself and we will organize a tailored live demo to show how you can power up your clinical trials processes with Flex Databases.