Summary: Med Devices provides clinical research and clinical trial management services. We offer innovative service from planning to market authorization to our customers in pharmaceutical, biotechnology and medical device industry.
Press Release: – Monday, Vasundhara,Ghaziabad, July 26TH, 2011 www.meddevices.net (India) form provide manufacturers of medical device, all over the world with well adjusted and flexible service packages, to support its clients to comply with European legislation. In Middle of year 2009, medevices has started different operation in India with purposefully located branch office- covering India, as independent Clinical Research Organization (CRO) that provide quality services to Biotechnology, Pharmaceutical and Medical Device Industry
Med devices offers innovative and creative full services from first step, planning to market authorization means a CE marking certification , to the customers in pharmaceutical, biotechnology and medical device industry. The CE mark is given by consumers everywhere as a symbol of safety and quality, it’s not only necessary in Europe, but also it can help to sell the product. CE mark is required for many products and their different categories of different products. Many rules and regulations are required for this certification. A european authorised representative can be exceptionally helpful in determining about the need of one’s product and only they know all the the procedure and paperwork.
It firmly believes in clearness in communication with their clients related to their projects. The last five years, have also witness an incredible interest and activity in the area of clinical research services in India. Meddevices.net also performs clinical trials in strict observance to ICH-GCP committed to a very high position of protocol conformity and responsive to critical communication between site, study personnel, sponsor, IRB, and other interconnected trial entities.
About meddevices.net: MED DEVICES has an exposure of serving the Industry with different services, such are contact or Clinical Research organization Services ( from Phase II to Phase IV) to Pharmaceutical, Medical Device /Biotechnology Industry, Representation Services i.e. European Authorised Representative (EAR) from U.K. office ,also to Medical Device manufacturers over the world against mandatory requirement of EU Directive, Third party Inspection Services and Medical Devices Quality Management Services (MDQMS), CE Marking certification of Medical Devices.
For more details about CE mark, Clinical Research organization and other services visit www.meddevices.net
India Corporate Office
Med Devices Lifesciences Private Limited
SF 207- 208, 2nd Floor,
Commercial Plot No. 1,
Sector- 5, Vasundhara,
Ghaziabad- 201 010 (Delhi NCR)
E-mail: [email protected]