Insights and guidance
Our goal is to provide you with the information you need to get the job done.
eTMF software has become more than a storage container for TMF documentation. In this joint whitepaper with our client, DZS Clinical Services, we discuss how clinical trial sponsors and contract research organizations (CROs) can work together using an electronic TMF as a hub for collaboration and coordination to increase quality and improve efficiency.
This ebook is for clinical site leaders who plan the transformation of their businesses using technology. It is designed to help you develop your thinking, strategy, and plan for implementing systems.
Learn about the types of clinical operations technology, what you need to consider when adopting new technology and the five steps for a successful implementation.
Check out the ebook version of our in-depth whitepaper on the four generations of electronic trial master file (eTMF) software.
Learn the key differences between each generation of eTMF software and how the fourth generation makes it easy for your teams to work quickly. You’ll also learn the ten key attributes of a 4th generation eTMF application.
In the summer of 2020, Agatha surveyed sponsors, CROs, and clinical sites to understand where they stand today in their use of remote processes technologies and their plans going forward.
In this report, we cover the results of our survey and provide insights and guidance into the state of remote monitoring and quality processes in clinical trials.
While the ability to monitor clinical trials has traditionally been performed through in-site visits, there has been much discussion about the idea of remote site monitoring. COVID-19 and the resulting restrictions on travel have brought the remote monitoring discussion to the forefront.
In this technology guide, we look at the role of remote monitoring in clinical trials, the activities performed, and the key capabilities you need in a technology solution.
From our work with a number of sponsors, CRO, and site organizations, there are five key things you need to do at the site level to ensure success when transitioning to remote monitoring and Clinical Trial Management.
Download this guide to get an overview of standard operating procedures (SOPs), why they are essential, and how you can create and use them in your organization. We also provide a list of the key requirements for a solution to manage your SOPs.
Managing the trial master file for a clinical trial is complicated. You have participants working in different roles, and at different locations. And then there’s the process itself, which includes extensive document creation, review, and approval processes.
Download our guide to learn about the evolution of eTMF systems and how this new 4th generation eTMF provides a complete, easy-to-use, low-cost, application for managing your TMF.
The best way to know if an Agatha Application meets your needs is to try it out. And good news - we offer a free trial.
Complete the form, select the application you would like to try and we'll reach out to get you set up as quickly as possible.
Want a little more information on your trial process? Go here.