by Barb Mosher Zinck | Oct 20, 2021 | clinical trial software
Boston, MA, USA; Lyon, France; Tokyo, Japan. Agatha Inc. announces that Gustave Roussy, the first oncology center in Europe, has selected Agatha to assist with the remote verification of patient Informed Consent. Pour lire ce communiqué de presse en français, veuillez...
by Ken Lownie | Oct 7, 2021 | clinical, clinical trial software
Clinical Operations as a distinct corporate function and department has evolved into a standard corporate model at sponsor and CRO companies, with all the trappings: Titles (e.g. Director of ClinOps), standard roles, its own language, a bevy of software...
by Barb Mosher Zinck | Sep 10, 2021 | clinical, clinical trial software
With so many eTMF solutions available today, how do you know which one is right for you? Many of these solutions provide similar features and functionality but there are ten requirements of a modern eTMF solution that you need to look for. And we’re providing...
by Barb Mosher Zinck | Aug 26, 2021 | clinical trial software, life sciences applications
You’re having trouble managing the trial master file for your clinical trial. But how do you know if you need an electronic master file (eTMF) solution to help? It may seem like a simple answer, and maybe it is – if you’re looking at the right things. Here...
by Ken Lownie | Aug 18, 2021 | clinical trial software
There is a lot of discussion about taking ownership of the trial master file (TMF). We wanted to understand what was behind this thinking of sponsors bringing the TMF in-house, so we reached out to an industry maven, Janine Penman of JPScientific, to fill us in. Who...
by Jill Heinz | Aug 11, 2021 | clinical trial software
Adopting clinical operations software can be an enormous undertaking, and there are many aspects that a sponsor, CRO, or clinical site will want to address before taking this step. 1. Do Your Research Before Adopting Clinical Operations Software Start with defining...
