Medace B.V.
Too many promising medical innovations never reach the market or the patient. One of the hurdles to take is finding your way through the ever more stringent and difficult landscape of medical devices and cell therapy (GMP) legislation and technical validation.
Medace offers a full service work-learning environment where customers (being academics or entrepreneurs) are guided in how to set up and develop the technical dossier needed for clinical validation whilst producing their clinical grade product. Medace works with an EN ISO 13485:2016 certified quality and service package available for our customers on a use by need basis.
Medace provides:
• Specialized infrastructure (e.g. ISO7 and 8, and Class C and B cleanrooms)
• Validated and specialized equipment
• Quality Management System
• Trained professionals for hands-on guidance and support during development and validation
• Dedicated in-house training programs
Medace offers a full service work-learning environment where customers (being academics or entrepreneurs) are guided in how to set up and develop the technical dossier needed for clinical validation whilst producing their clinical grade product. Medace works with an EN ISO 13485:2016 certified quality and service package available for our customers on a use by need basis.
Medace provides:
• Specialized infrastructure (e.g. ISO7 and 8, and Class C and B cleanrooms)
• Validated and specialized equipment
• Quality Management System
• Trained professionals for hands-on guidance and support during development and validation
• Dedicated in-house training programs
Search Medace B.V. on Biomaterial Database Profil de l'entreprise
- Année de fondation
- 2018
- Portée du Marché
- International
- Type d'association
- Profit
- Type de certification
- Privé
- Website
- http://www.medacespace.com
Certifications
-
ISO 13485
Contacter le fournisseur Vous avez une question ou une demande ?
Gaetano Martinolaan 63
6229 GS Maastricht
Netherlands
Marché
- Europe