Serving both the In Vitro Diagnostic and Medical Device industries, MDSS specializes in European regulatory affairs. MDSS acts as “Authorized Representative” according to the European regulations for the EU, UK and Switzerland.
Certified to EN ISO 9001, we consult on quality-/risk management systems and all related services to achieve CE and UKCA-approval. MDSS provides customized services for product registration, incident reporting, recall management, labelling, technical files, among others.
Additional Info
We will be displaying a new product or promoting a new indication/enhanced feature for an existing product in our booth?
No