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Accelerate biomedical innovations. Together.

Too many promising medical innovations never reach the patient due to the ever more stringent and difficult landscape of Medical Devices and Advanced Therapy Medicinal Products 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?

Certified Quality Management System

Flexible renting of cleanrooms and research labs

Validated equipment

Technical, GMP and ISO expertise

Dedicated training program by in-house professionals

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. And offer you the GMP and ISO cleanrooms to produce your own product.

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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.

RiboPro GMP techniciansSuccess Stories
7 December 2022

RIBOPRO launches GMP factory for (m)RNA

Over the last two years RIBOPRO has slowly but surely build up a reputation with the production of high-quality messenger RNA (mRNA) products. The fast delivery, complete service and in-depth knowledge…
PoSTuRE, InSciTe, clinical trial scoliosis treatmentSuccess Stories
5 October 2021

Chemelot InSciTe starts first-in-man clinical trial for novel scoliosis treatment

Medace's client Chemelot InSciTe, announces that they have started the first-in-man clinical trial for a new scoliosis treatment within the project PoSTuRE (Patient Specific Scoliosis Treatment). The treatment consists of a…
RegMed XB, Aart van ApeldoornSuccess Stories
22 January 2021

Medace lowers the threshold for researchers of RegMed XB

RegMed XB stands for Regenerative Medicine Crossing Borders. It is a virtual institute of Dutch and Belgian public (universities and governments) and private (health foundations and companies) partners that will work…

Let’s meet!

Interested to join our community? Got some questions you want answered? Thinking of renting your own space at Medace?

Plan your meeting with CBO Kurt Gielen now.

Get in touch
Kurt Gielen

News and resources

Advanced-Therapies 2023EventsNews
10 February 2023

Advanced Therapies 2023

The Advanced Therapies Congress is Europe’s largest cell and gene therapy conference and exhibition. The event is for the leaders of the world’s ATMP developers and their most senior executives in charge…
5 December 2022

EIC – EMA Info Day: Regulatory support for the development of innovative medicines and technologies – January 31, 2023

Join this online EMA Info Day: Regulatory support for the development of innovative medicines and technologies and discover the wide range of support services that the European Medicines Agency (EMA) provides…
7 September 2022

CLOSED – Job opportunity: Biotech associate

07 September 2022 – Job opportunity Biotech associate at Medace Please note that this job opening has been filled, you can no longer apply for this position currently. About Medace Medace is…
See all news and resources

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