Too many promising medical innovations never reach the patient due to ever more stringent and difficult landscape of medical devices and cell therapy (GMP), legislation and technical validation.
Medace is committed to bring your innovative (bio)medical concepts to the market and patients faster.
What’s in it for you?
What do we offer?
We offer a work-learning environment that allows you to develop your technical product dossier needed for clinical validation. At the same time we guide you in how to produce your product according to the ISO and GMP standards.
With a broad range of training, expertise and support we provide everything you need to know about regulatory, quality assurance, technical development and so much more. We guide you through the set up and development of technical files. Quality is guaranteed as everything is covered under our overarching ISO certificate.
From flexible office spaces to R&D labs and specialized cleanrooms with validated equipment, a full Quality Management system and trained personnel, at Medace you find everything to develop and manufacture your clinical grade product.