The Power of CTMS Website Integration

Why your CTMS needs website capabilities

Managing your website and keeping it up to date is already a painstaking process but managing your study listings on your website can be even more time-consuming and costly. This is especially true if you pay a website management company to add/remove studies for you.  The good news? RealTime-CTMS has an option to link your … Read more

A RealTime to Reflect

A realtime to reflect

The clinical research and pharmaceutical industry could never have expected the events of 2020. With clinical trials being mostly paused for part of the year, the adoption of social distancing practices, travel restrictions, and the intense search for COVID-19 vaccines and treatments in full swing, our industry has adapted to keep research moving through it … Read more

3 Tips for Staying Audit-Ready

3 Tips for Staying Aduit Ready

Maintaining audit-readiness is the best way to ensure that your site is prepared for audits and inspections, both planned and unplanned. This proactive approach prevents headaches and last-minute scrambling by staff in the event of an actual audit.  The following tips will help you ensure that your team is audit-ready. Create Create and establish an … Read more

The Case for Standards in Site Regulatory

Site regulatory standards

The development of standards is a proven methodology for efficiency and quality. By implementing an eRegulatory solution, research institutions have the opportunity to standardize clinical trial documentation and processes.

Announcing Enhanced Integration with RealTime CTMS

Announcing Enhanced Integration with RealTime CTMS

CHAPEL HILL, NC (October 7, 2020)- Devana Solutions, LLC is pleased to announce that the API-integration of Devana IGNITE with RealTime CTMS has been enhanced in support of both companies’ mutual customers. Devana IGNITE provides clinical research organizations is the leading cloud platform for pipeline administration, pre-clinical workflow automation and metrics capture and analytics. Devana … Read more

San Antonio-based software company is changing the face of the clinical trial industry

Remote manage your trials with RealTime

San Antonio-based software company is changing the face of the clinical trial industry RealTime Software Solutions is introducing DecenTRIAL, a site-friendly decentralized study platform that allows Sponsors and CROs to manage clinicals more efficiently, remotely and without the need for costly EDC systems. San Antonio, TX – In a world becoming more and more virtual, … Read more

Transition and Adaptation of Clinical Research in 2020

A letter from Rick Greenfield

Wow… 2020 has been a year of adaptation on a level that none of us could have predicted.  As we celebrated last New Year’s Eve with the excitement of what 2020 would bring, none of us knew what we were in for! But here we are, proving that we are even more resilient than we … Read more

Part 3: How Coastal Pediatric Trained Staff on an eRegulatory Solution

Training on an eRegulatory Solution

We explore Coastal Pediatric Research’s journey to adopting Complion’s eRegulatory solution which has enabled the site to increase efficiency, greatly improve time management, and eliminate duplication of work while conducting their clinical research studies. In the last post of this three-part series, we take a look at the training phase when adopting an eRegulatory solution.

Why it’s important to choose the right CTMS the first time

Choosing the right CTMS

Choosing the right Clinical Trial Management System (CTMS) takes careful evaluation requiring a substantial time investment as well as extensive research. When choosing a CTMS, you should feel confident that you are making the right decision, as the wrong decision can be very costly to your organization in the short-term, resulting in long-term consequences. The Depth … Read more

Part 2: How Coastal Pediatric Implemented an eRegulatory Solution

How Coastal Pediatric implemented an eRegulatory solution

We explore Coastal Pediatric Research’s journey to adopting Complion’s eRegulatory solution which has enabled the site to increase efficiency, greatly improve time management, and eliminate duplication of work while conducting their clinical research studies. In the second of this three-part series, we take a look at the implementation phase of the adoption of an eRegulatory solution.