Clinical trials continue to be burdened with paper and manual processes. Sometimes hybrid situations are used where there are some paper processes and some manual processes. Either system (all manual or hybrid) makes clinical trial documentation challenging as it is not all digitized. However, the challenges are easily overcome by implementing digital documents with workflow …
By Guest Author: Dr. Karin Köhler-Hansner As a sponsor, do you contract out your clinical trials to a CRO and forget about them? Do you expect that once you sign the Transfer of Obligations form that you can relax and look forward to a perfectly packaged up final study report? You may want to rethink …
The Importance of Sponsor Oversight in Clinical Trials Read More »
This is the first in a series of blog posts sharing the expertise and voices of SureClinical employees, advisors and customers. This blog is focused on how a seasoned CRA chose the best eTMF and CTMS system. We welcome your feedback and your own experiences about your own digital journey. As a consultant CRA with more than …
A CRA’s Digital Journey, aka How I Learned to Love my eTMF Read More »
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