Lexology Getting The Deal Through: Pharma & Medical Device Regulation 2020

The first edition of another handbook, for which our senior partner Prof. Ehlers is also co-editor, provides a comprehensive overview of the latest legal and regulatory developments in different countries in comparison. Among the central topics are: Healthcare regulatory frameworks and competent authorities; clinical practice; marketing authorisation; changes in marketing authorisations; recalls; enforcement of advertising regulations; pricing and reimbursement; off-label use and unlicensed products; and sales and delivery.

Here you can read the country chapter Germany Pharma & Medical Device Regulation

Reproduced with the kind permission of Law Business Research Ltd. The article was published in December 2019 in the series Lexology Getting the Deal Through – Pharma & Medical Device Regulation 2020. For further information please visit www.gettingthedealthrough.com