November 1, 2021
In this video, we’ll tell you about Flex Databases CTMS & eTMF implementation for FGK CRO. We’ve reviewed the case study before, you can find the text version here.
Timecodes:
00:19 About Flex Databases
00:46 VIdeo plan
01:00 About FGK CRO
01:44 Project Scope
02:00 Project timeline: Preparation stage
02:30 QA environment
02:54 Production delivery
03:15 Feedback from the client
03:54 Contact us
We are driven by our high mission to make an impact in the Life Sciences industry. We provide flexible e-Clinical software systems for Clinical Research Organizations (CROs) and pharmaceutical companies. We work globally with clients all over the world, with our own offices located in the Czech Republic, Switzerland, Turkey, and the US. About the […]
When preparing a tender for a Clinical Trial Management System (CTMS) and an electronic Trial Master File (eTMF), CROs must choose solutions that meet sponsor expectations and improve operational efficiency while keeping studies inspection-ready. The right choice affects study delivery, compliance, and client satisfaction. Below are the key factors CROs should consider. Regulatory Compliance and […]
How Flex Databases connects your study ecosystem – reliably, securely, and at scale. Why integrations matter to sponsors and CROs Integration means that data entered once in a system of record is propagated automatically wherever it is needed. For clinical operations teams this translates into: Core integration patterns we see most often 1) EDC → […]
In July 2025, the European Commission adopted Commission Implementing Regulation (EU) 2025/1466, amending Regulation (EU) No 520/2012. The changes aim to strengthen pharmacovigilance, reduce unnecessary administrative burden, and align EU requirements with global best practices. Most provisions apply from 12 February 2026, with certain Eudravigilance updates taking effect in August 2025. Why the Changes Were […]
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