An International Quality Systems and EU Directives Implementation Service
for the Medical Devices and In Vitro Diagnostics Industries
for all Class I, Class IIa, IIb, Class III Devices & IVD's

QualiMedd is an independent, UK based consultancy established early in 1990 and working mainly within the areas of Product Development, Regulatory Affairs and Quality Improvement. We specialise in the Medical Devices and In Vitro Diagnostics industries in both development and manufacturing companies and sales and service companies.

We offer a professional service specifically designed to assist both start up and established companies and have worked with organisations ranging from one man companies to corporations employing thousands worldwide.

Experienced in the requirements of the regulatory bodies and both manufacturers and customers, QualiMedd offer technical guidance to clients in all areas, from the explanation of requirements, through preparation of detailed plans for product development including quality and regulatory systems, through assisting with the documentation and implementation of processes and procedures to assisting with regulatory approvals.

Last Updated Oct. 2008
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