Medical technology covers both medical devices and human tissue products. A medical device is an object or substance used for diagnosis or treatment of disorders or handicaps. This might be X-ray apparatus or infusion pumps, as well as rollators and hearing aids. Examples of human tissue products are donor tissue or artificial skin for use in regenerative medicine or in the treatment of burns. What is RIVM’s role in medical technology?
RIVM carries out laboratory research, and desk and field studies, on quality and safety of medical products. Areas of interest include sterilisation (re-use of medical devices) and prevention of disease transmission, bio-compatibility and assessment of medical device dossiers. Another activity is reviewing the processes around purchase of medical devices. New and emerging technologies, such as nanotechnology, are actively followed by the RIVM. Who does RIVM work for? RIVM expertise is used by researchers and professionals in medical technology, and by government bodies. The Health Care Inspectorate and the Ministry of Health, Welfare and Sport (VWS) receive both structural and ad hoc advice in the field of medical technology, and are constantly informed about new trends. Besides this, RIVM contributes to national and European legislation and represents VWS in standardisation committees, thus contributing to (inter)national standards on the safety of medical devices and medical technology.
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