In Vitro Diagnostic Medical Devices: Law and Practice in Five Eu Member States (Hardcover)

From the Publisher: A guide for in vitro diagnostic medical device manufacturers who are interested in selling their products in Europe, providing a systematic comparison of the laws regarding the development, production, distribution, and use of such devices within the five states. The coverage is both very specific and selective, including the general features of the national requirements, different product classes, placing devices on the market, the conformity of business operations, distribution to the patient or user, and post-marketing control. Based on a report requested by the European Commission. No index. Annotation copyright Book News, Inc. Portland, Or.