Rule over your eTMF: how to optimise the electronic master file
Introduction The Electronic Master File (eTMF) is one of the most important components of Clinical Research and needs to be perfect. Donât let it be the last thing you think about in your clinical trial. Are you looking for the right way to manage your eTMF? Youâre in luck. In this article, you will learn […]
What is a risk-based approach to TMF management?
The trial master file (TMF) is one of the most important components of clinical trial management. The TMF contains all the essential documents related to a clinical trial, including the protocol, ethics approval, informed consent forms, case report forms, study procedures, data management, statistics, and more. Maintaining a complete, accurate, and inspection-ready TMF is crucial […]
Electronic Trial Master File (eTMF): Why & How To Choose For Your Digital Trials
The management of clinical trial documents and data is a crucial aspect of running efficient and compliant trials. Paper-based systems have significant limitations – they are cumbersome to manage, prone to errors, and lack real-time visibility. This is why electronic Trial Master Files (eTMFs) have become the preferred choice for streamlining clinical trials in the […]
