Quality Management Services
Our QM division provides support and services to ensure high product quality and compliance with current valid guidelines and regulations for products used in the pharmaceutical industry — such as APIs, intermediates, excipients, bulk products and finished dosage forms.
Midas conducts on-site assessments of manufacturing facilities, conducts follow-up activities, offers support — for example, gap analysis and mock inspections — and ensures continuous improvement of GMP compliance.
Midas Pharma is a pharmaceutical service provider and holds a Manufacturing License issued by the competent German authority, an Import License for products within the scope of §72a of the German Drug Law (i.e. AMG). Midas Pharma is certified according to FAMI-QS requirements (European Code of Practice for Feed Additives and Premixture Operators).
We set high standards for the qualification of our quality management staff. The vast majority of the employees on our Quality Team have a university degree and experience in different areas of pharmaceutical companies. Regular internal training maintains high levels of competence. Our highly qualified auditors perform around 80 on-site assessments per year, issuing 60 paper assessments. Seven QM experts in our German headquarters and an additional ten QM experts worldwide continuously maintain and improve our Quality Management System. Our German headquarters is audited several times a year by our customers.