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New Additions to the encapsia® New Generation Clinical Data Suite
07 Feb

New Additions to the encapsia® New Generation Clinical Data Suite

07 Feb 2017

Cmed, an innovative technology-led CRO, has made further enhancements and additions to encapsia®, the first App based new generation clinical data suite. The latest Apps added to encapsia® improve its ability to provide efficient, enterprise level CDMS, alongside its eSource, web eDC, insights and analytics functions. All these functions being provided in a unified, cloud platform designed specifically to improve the speed and quality of data whilst minimizing unnecessary complexity and ultimately cost associated with these processes....

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Cmed Presents New Generation Technology to Speed and Streamline Clinical Trials at Dpharm Europe
31 Jan

Cmed Presents New Generation Technology to Speed and Streamline Clinical Trials at Dpharm Europe

31 Jan 2017

Cmed, an innovative technology-led CRO, today announced its participation at Dpharm Europe: Disruptive Innovations to Advance Clinical Trials (8-9 February 2017, London), where it will showcase its cloud-based, new generation clinical data suite, encapsia®. Graham Belgrave, Chief Operations Officer at Cmed, will introduce encapsia® in the “Innovative Sources & Solutions: Quickfire Disruptors” session on Wednesday 8 February between 4:30pm and 5:00pm, and highlight how a truly flexible, new seamless approach can simplify and streamline clinical trials....

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The Unattainable Trilogy of Monitoring?
01 Nov

The Unattainable Trilogy of Monitoring?

01 Nov 2016

Upcoming Webinar: Risk-Based Monitoring, Remote Monitoring and eSource: The Unattainable Trilogy of Monitoring? A ‘Smart Monitoring’ Approach On Tuesday, November 22, 2016, Xtalks will host a complimentary webinar featuring Graham Belgrave, Chief Operations Officer at Cmed and Jon Carter, Product Manager at Cmed, as the keynote speakers. Over the last decade, the number, complexity and cost of clinical trials has increased dramatically. This means even more challenges for sponsors as they continue to meet their obligations to patient safety, data integrity and regulatory compliance, whilst in turn trying to control costs and shorten timelines....

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Why eSource?
25 Oct

Why eSource?

25 Oct 2016

The word “eSource” is second only to “wearables” in buzz worthiness this year. Every top ten pharma I have spoken with has an eSource initiative or committee dedicated to studying eSource. But why? Is it necessary? Will it reduce timelines? Can eSource have a real effect on the bottom line? After all it was not that long ago that all that eSource is promising was being promised by another new idea, eDC....

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DPharm 2016 – Clinical Research, Is there an app for that?
13 Oct

DPharm 2016 – Clinical Research, Is there an app for that?

13 Oct 2016

There was a time when the term ‘app’ referred to very simple and, often less powerful version of a full web or PC based ‘application’ but those days are long gone. Today, you can order a pizza to be delivered to your friend’s house, hail a ride to meet it there, and have your friend split the bill… all from the comfort of your smart phone or tablet. Many apps today actually outperform their ‘full’ version counterparts by utilizing powerful features found in our mobile devices like GPS and cameras....

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