MED DEVICE LIMITED (U.K.) was formed to provide medical device manufacturers world-wide with flexible and well adjusted service packages to assist its clients to comply with EU legislation. In Mid- 2008, we started operation in India (as M/s Med Devices Lifesciences Pvt. Ltd.) with strategically located branch office- covering India, as independent Contract Research Organization (CRO) providing quality services to Pharmaceutical, Biotechnology and Medical Device Industry. MED DEVICES has a vision of serving the Industry By facilitating- Clinical Research Services (Phase II to Phase IV) to Pharmaceutical/ Biotechnology/ Medical Device Industry. Representation Services (EAR) from our U.K. office, to Medical Device Manufacturers worldwide against mandatory requirement of European Directive. MDQMS (Medical Devices Quality Management Services- ISO 13485: 2003) Product Certification (CE Marking) of Medical Devices US FDA consulting services to Medical Device Manufacturers Third party Inspection Services We perform clinical trials under strict adherence to ICH-GCP dedicated to a high level of protocol compliance and responsive to critical communication between sponsor, site, IRB, study personnel, and related trial entities. We are dedicated to offer creative and innovative full service from planning to market authorization, to our customers in pharmaceutical, biotechnology and medical device industry.