Internal Audits - There's Always Room For Improvement
Audit. The one word that strikes fear in many a clinical trial professional’s hearts. While we have the IRS to thank for giving the word “audit” a bad name, it doesn’t have to be scary or sinister.…
Changing Industry Expectations: A CTMS Platform with Rapid Startup and Easy Configurability
In our previous blog post we discussed the tradeoffs made between software solutions offering turnkey, rapid startup models, and those with deeper functionality and high levels of configurability. In…
Changing Industry Expectations: Why do turnkey solutions sacrifice configurability?
In this blog post we’re aiming to discuss a prominent cost-saving strategy in clinical trials and how it interacts more generally with beneficial qualities of technology offerings that serve the…
Do you know what SOC Compliance is and why it is important that your eClinical vendors have one?
When evaluating a vendor, especially a technology vendor, certain items are expected like security and compliance. One of the ways to ensure a vendor is secure and compliant is being SOC 2® Type II…
'Everything has changed': Managing complex clinical trial data
originally published 20 -Mar-2019 By Maggie LynchAs clinical trials create large amounts of data, and researchers seize the opportunity to use de-identified data as a means to develop and discovery,…
Datatrak launches system for unifying imaging capture and adjudication workflows
Originally Published February 18, 2019by John R. Fischer , Staff ReporterThis article has been reposted with permission from HealthCare Business News Datatrak International launched the first…
Customer Experience Questions to Ask Your eClinical Vendor
When choosing an eClinical vendor, it is important to understand the customer service/experience they will provide. The primary focus of any evaluation will naturally be the features and functionality…
3 Ways CTMS by Datatrak can Maintain Better Communication Within Your Organization
From our inception, a priority for Datatrak is to empower work group teams with role-based access to version-controlled file management, calendar events, tasks and contacts, all built within our…
Simplifying the Regulatory Submission Process With A Modern CTMS
Simplifying the Regulatory Submission Process with a Modern CTMS Our CTMS Product Manager, Patrick Smith, will be presenting an @ACRPDC Webinar! Sign up and learn more at bit.ly/2sT3hYo.This session…
Global Standards in Medical Device, Technology Development
By Dr. Bill Gluck, Vice-President, Clinical KnowledgeRecently, the European Forum for GCP (EFGCP) and MedTech Europe established a Medical Technology Working Party to promote the collaboration of…