medical devices

Regardless of whether it is about electric toothbrushes, implants or combination products - the application of GMP, the Good Manufacturing Practices, is also necessary in the manufacture of class I, I m, r, s IIa, IIb, III medical devices and for combination products . The term "GMP" is not so firmly established here - but the topics behind it are.

With the range of compliance consulting services for medical technology, medcycle provides targeted and effective advice and support throughout the entire life cycle of the medical device, such as design and development, production management, supplier controls or post-market surveillance.

Cross-industry practical expertise and current management and regulatory knowledge are brought in to provide tailor-made concepts and continuous support in the development and implementation of quality management systems and during daily routine.

medcycle acts as a quality consultant and is an experienced and competent implementation partner when it comes to implementing the specific requirements of the various product areas in a solution-oriented and efficient manner.