ma meditec supplies the medical equipment industry with assembly systems for medical devices (such as contact lenses, stents, inhalers, insulin pens and auto-injectors) and also offers services relating to compliance with quality guidelines and validation in medicine and pharmaceuticals production (‘GMP documentation‘).
Our user-focused process support, GMP-compliant design, extensive approval and certification experience – backed by the selection of precisely the right technology and competent system partners – are genuine value-adding factors operating to the benefit of our customers.
MA micro automation GmbH has a quality management system which is certified to ISO 9001:2015 and is based on the GMP guidelines.
The certificates are available in Downloads.
GMP with MA micro automation GmbH
Support by MA micro automation
We assist you in request detection, risk assessments, system configuration, testing, service and maintenance. Compliance with the expectations of regulated companies in the medical and pharmaceutical industry is our main goal.
We provide you the necessary documents for the qualification documentation (DQ, IQ, OQ) of our developed, manufactured and delivered plant and assist you in the validation.
The necessary tests for the qualification will be put to a test plan with the customer according to the VMP (Validation Master Plan) and take place at our premises or at customer's site.