HORSHAM, England--(BUSINESS WIRE)--Cmed Clinical Services announced today it will be presenting at the European Clinical Data Forum being held from 7th - 8th May 2014 in Brussels, further cementing the company’s position as an industry leader in innovation and clinical data.
Harshad Sodha, Cmed’s Senior Director, Global Clinical Data Management, will address the principles of eSource and the impact of various regulatory guidance documents in his presentation titled “The Practical Realities of eSource: A Real World Experience”, which will take place on 8th May 2014 at 11.30am. In this session, Sodha will describe the practical implementation of an integrated eSource/eCRF solution and assess the impact on site monitoring and clinical data management activities. The presentation will examine the benefits, both in terms of time and cost savings, and the limitations of eSource implementation.
Sodha joins a wide array of senior industry speakers at this two-day conference, bringing together expert knowledge and experiences in data integration and data transparency, new areas for technological innovation and the changing regulatory environment.
Attendees are also encouraged to visit Cmed on booth #8, where there will be an opportunity to meet with Sodha and learn more from Cmed executives.
Cmed Clinical Services is a full service, global CRO specialised in the design and delivery of traditional, innovative and/or complex early Phase I to IIb clinical trials, as well as Phase III studies. Cmed accomplishes this through the coupling of full service trial delivery teams and trusted technology, as well as providing stand-alone functional service, client specific solutions across all its services, such a clinical data management and biostatistics.
To pre-arrange a meeting with Cmed during the European Clinical Data Forum or for further information about Cmed’s complete range of CRO services, including its Functional Service Provision (FSP) capabilities, email info@cmedresearch.com.
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About Cmed Group (www.CmedGroup.com)
Cmed Group is an innovative clinical trials services and advanced software provider which includes two divisions: Cmed Clinical Services and Cmed Technology.
Cmed Clinical Services (www.CmedResearch.com) is a CRO that provides full service trial delivery teams (project management, clinical monitoring, data management, biostatistics, medical affairs, regulatory, consulting, and medical writing services) as well as stand-alone solutions across all its services, including Biometrics functional services. It combines experience with using many commercially available technologies but also uses trusted and innovative software developed by Cmed Technology, including its award winning system, Timaeus.
Cmed Technology (www.CmedTechnology.com) offers Timaeus: a single platform for electronic trial design, paper and electronic data capture, monitoring, coding, data management and reporting. Timaeus, which uses advanced distributed cloud computing and mobile technologies, is designed to respond on-demand to the needs of investigators, data managers and study teams. Timaeus has been used in every phase of clinical research – including early phase, pivotal and late phase studies as well as in emerging markets.
