The European Union decided to update the Medical Device Directive 93/42/EEC to the new Medical Device Regulation 2017/745. What are the changes? I’ll explain you everything on this article
A new obligation to perform an unannounced audit with Medical Device manufacturer created a lot of problems to any notified body. Resources not available, tight timeline. It is not easy for them but also to Medical Device Manufacturers.
Learn the DICT methodology to perform a Merger & Acquisition compliance review for a Medical Device Company. 3 Steps critical for a successful M&A.
Compliance is one of the aspects that are not well performed when taking over a new company.
