HORSHAM, England--(BUSINESS WIRE)--Cmed Clinical Services, an innovative, full service CRO providing services to the Biopharma industry worldwide, is exhibiting at the Outsourcing in Clinical Trials West Coast conference which is taking place on the 3rd- 4th February 2015, Burlingame, California, USA.
Cmed is ideally placed to help small Biopharma who are planning a clinical project by coupling its deep understanding of the challenges facing small Biopharma together with experience of building successful relationships. Visitors to Booth 33 will have the opportunity to learn about Cmed’s extensive knowledge and capabilities. Cmed recognises the massive impact on medicinal research being made by small Biopharma and remains passionate to help them succeed.
Attendees will be able to find out about the company’s full suite of services, which ranges from full-service to stand-alone solutions and functional services, such as biometrics. Cmed has invested heavily in recent years in its in-house drug development capability which is frequently utilised to provide consulting services to Biopharma companies to help them design clinical development plans and protocols in order to accomplish their objectives. Furthermore, Cmed has reinforced its commitment to meet the needs of the Biopharma community since opening its office near the heart of San Francisco’s biotechnology hub.
Cmed has earned a strong reputation for delivering complex and innovative clinical trials across numerous countries worldwide. While its strengths lie in oncology and rare disease, Cmed has amassed experience across a number of other therapeutic fields including neurology, cardiovascular, respiratory, infectious disease, endocrinology, gastroenterology, dermatology and ophthalmology.
If you would like to arrange to meet with a representative of Cmed at Outsourcing in Clinical Trials West Coast, or find out more about any of Cmed’s services, please do not hesitate to contact email@example.com.
Cmed is an innovative full service CRO and a software developer of smart e-clinical data capture and management technologies. Cmed was established in 2000 with the vision to conduct clinical trials better than anyone else, thus saving and helping lives. Cmed has a focus on bringing innovation to the design and conduct of clinical trials, including in the areas of clinical data capture, data management, monitoring. Cmed has two divisions: Cmed Clinical Services and Cmed Technology.
Cmed Clinical Services is a global CRO providing services to the Biopharma industry worldwide. Cmed works with clients to not only deliver the clinical trial services effectively, and with quality, passion, teamwork and superior customer service, but also, especially for full service projects, by understanding the clients commercial and business objectives. Cmed then leverages its in-depth expertise to ensure the development program and/or clinical trial is well designed and conducted as efficiently and as cost effectively as possible. Cmed has particular expertise in the design and conduct of complex, oncology and rare disease trials and the provision of Biometric functional services.
Cmed Technology designed and developed Timaeus: a unique single platform for electronic trial design, paper & electronic data capture, monitoring, coding, data management and reporting. Using distributed cloud computing and mobile technologies, Timaeus has been deployed in over 400 clinical trials and has successfully passed multiple audits. The unique Timaeus design provides a number of benefits to our clients including rapid database build (weeks not months), mid-trial updates without down-time and non-reliance on the internet. These benefits lead to many advantages including the removal of EDC build from study start-up, no restriction on investigator site selection, no negative impact on recruitment timelines due to design changes, and elevated investigator motivation.