Reprocessing validations are essential to ensure that medical devices are safe for the intended use and reuse. Manufacturers must ensure that their products are clean and sterile before it becomes available in a healthcare setting.
Christine Laube has over 14 years of experience in microbiology testing and the medical device industry. In her current role as Medical Product Expert and Biological/Analytical Testing Specialist at TÜV SÜD, Christine is responsible for technical documentation review of MDR submissions and facilitating biological and chemical testing services.
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Bosnia and Herzegovina