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Cmed shows encapsia® at 2017 ASCO Annual Meeting
19 May

Cmed shows encapsia® at 2017 ASCO Annual Meeting

19 May 2017

Cmed, an innovative technology-led oncology CRO, today announced it will be exhibiting at the 2017 American Society of Clinical Oncology (ASCO) Annual Meeting in Chicago, Illinois (June 3-5), and showing how encapsia® can help improve patient safety, study conduct and decision making in oncology clinical trials (Booth 23128). Cmed has earned a strong reputation for successfully conducting oncology trials across all phases and in numerous cancer types, including breast, lung, prostate, colorectal and other solid cancers, and haematological malignancies....

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eSource Bootcamp- Wheel of Change
11 May

eSource Bootcamp- Wheel of Change

11 May 2017

4th eSource in Clinical Investigations Annual Bootcamp Sponsors, Sites, and Vendors converged on Philadelphia, PA last week to discuss the current status of eSource (Direct Data Capture) in clinical trials, the hurdles to overcome, and the future. Day one focused on the reasons to do more eSource in trials. Themes included bringing the data collection closer to the patient to reduce errors and how everyone from Investigators, that are currently doing double data entry, to Executive Management, that need to see data and understand the true status of their portfolio at any given time, will benefit....

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eSource Data in Clinical Investigations 2017
25 Apr

eSource Data in Clinical Investigations 2017

25 Apr 2017

Cmed, an innovative technology-led CRO, will present “Why eSource and what will it change? Accessing data in clinical trials” at the 4th Annual eSource Data in Clinical Investigations Conference in Philadelphia at 10.30am on Wednesday May 3rd, 2017. Graham Belgrave, Cmed’s Chief Operations Officer, and Product Manager Jon Carter, will examine the principles of eSource and how it has the potential to be a real “game changer” for trial conduct and for study team roles....

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Cmed Presents Smart Monitoring and eSource
27 Feb

Cmed Presents Smart Monitoring and eSource

27 Feb 2017

Cmed, an innovative technology-led CRO, will present “Risk-Based Monitoring, Remote Monitoring and eSource: The Unattainable Trilogy of Monitoring?” at the ACDM Annual Conference being held in Brussels on Tuesday, March 14, 2017. In this presentation, Stephanie Langouet, Cmed’s Vice President of Data and Analytics, will explore the practical implementation of more effective monitoring strategies, from traditional 100% Source Data Verification (SDV) to Risk-Based Monitoring (RBM) and increased remote review, and will assess the impact on site monitoring and clinical data management activities....

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Cmed Invited to Share Its Expertise at Upcoming Industry Events
17 Feb

Cmed Invited to Share Its Expertise at Upcoming Industry Events

17 Feb 2017

Cmed, an innovative technology-led CRO, has been invited to share its expertise in bringing innovation to the design and conduct of clinical trials at three leading industry events in February and March. Ami Israel, Cmed’s Vice President of Clinical and Regulatory Operations, will present at eyeforpharma’s Data and Technology in Clinical Trials Summit (February 21-22, 2017, Philadelphia) in a session titled “Move towards more flexible and cost-effective trials. The Power of Technology Driven Applications”....

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