Clinical Research Tech News

What to look for in a CTMS

Sites have a million things to deal with before, during and after a trial. Coordinators and staff have their plates full every day with paperwork, meetings and hundreds of emails. Starting a new study is not easy, but it can be a whole lot less stressful with the right CTMS. Choosing the perfect CTMS will […]

December 21, 2017 0 comment

The holidays are upon us. As Thanksgiving and Christmas approach, you’ll most likely see your patient retention rates drop. While we are all looking forward to the Holidays and spending time with loved ones, subject no-shows can have a negative effect on your trial and your site’s bank account.  So, how can you motivate your […]

November 14, 2017 0 comment
eSOURCE…We changed the game, AGAIN!

The clinical research industry has inevitably been slow to adopt technological advances primarily due to regulatory constraints and a fear of change that could disrupt current processes.  While the regulatory guidance has been issued by the FDA, development of solutions that can conform to the guidance AND improve efficiency is challenging. In the recent years, […]

October 26, 2017 0 comment
A mobile app that makes everything simple

As a clinical researcher, being at your desk to take care of study documentation, patient referrals and everything else that goes into managing your studies can be difficult and time-consuming.  That’s why our team has created a mobile app that lets you access all your files, contacts, patient referrals, and inclusion/exclusion criteria on the go. […]

August 25, 2017 0 comment
RealTime is Changing the CTMS Industry with First-of-its-Kind New App

Research sites can now access popular eDOCS solution on mobile device with new app SAN ANTONIO—Want to access site eRegulatory files, sign documents with your thumb print, refer a patient to a study or look up site and sponsor contacts all on your mobile device? There’s an app for that! RealTime-CTMS launched the first-of-its-kind new […]

August 14, 2017 0 comment
Paper Checks Riskier than You Think!

How many checks do you sign each day? Ten, twenty, fifty? You issue a check to your subjects after every visit but, how well do you know the person who will cash the check? Can you trust them with your information? Every issued check represents a higher risk of fraud for your company. It will […]

July 28, 2017 0 comment
What RealTime–TEXT Can do for YOUR Site!

As a RealTime-CTMS user, you are likely accustomed to the quick access that RealTime gives you to study and subject information. Our CTMS allows you to easily manage your subject data, study information, study visits, scheduling, financial data, reports, and more. But did you know RealTime also has a TEXT feature that fully integrates with […]

June 27, 2017 0 comment
eRegulatory – A Change Worth Making

Let’s face it, change is hard. You get used to the way you’ve always done things and when someone talks about doing something different, you’re like a deer caught in headlights. If you’re working at a clinical research site and have always used paper regulatory documents, changing to an electronic document solution may seem overwhelming […]

April 28, 2017 0 comment
realtime edocs outlook RealTime-CTMS Clinical Trial Management System
RealTime-eDOCS Now Integrates with Outlook!

Our industry-leading eRegulatory system just got better!  RealTime has built a custom Outlook add-in that integrates RealTime-eDOCS with your Outlook email.   RealTime-eDOCS customers now find it easier than ever to manage records and electronic signatures without leaving their email. Game-changing features include: Upload Emails and Attachments from Outlook to eDOCS Quickly upload files from […]

October 4, 2016 0 comment
Webinar RealTime-CTMS Clinical Trial Management System
Webinar Q&A From RealTime’s Product Manager Nathan Levens

Did you catch our webinar hosted by ClinEdge, “e-Regulatory Systems – Connecting Sites and Sponsors in a Whole New Way” from August? If not you can watch the recording here. Nathan Levens answered several great questions during the webinar and received additional questions after the webinar ended.  Below are some additional questions addressed after the webinar. […]

September 23, 2016 0 comment


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