From India to the EU: A Practical Guide to CE Marking for MedTech Manufacturers

​Planning to sell your medical device in Europe?

​Getting a CE mark is hard enough for companies based in the EU. Doing it from India adds distance, unfamiliar processes and a lot of documentation.

​In this 60-minute session, CertHub and its authorized partner for India, Inventicia, show how Indian MedTech manufacturers can get on the path to CE marking faster, with less rework and more clarity.

​What you'll learn

• ​What the route to a CE mark looks like for non-EU manufacturers under MDR and IVDR

• ​Where manufacturers most often lose time in technical documentation and quality management

• ​How CertHub's AI-powered compliance platform works: one structured regulatory data model as a single source of truth, reusable across markets

• ​How Inventicia supports Indian manufacturers on the ground

​Includes a live platform demo and Q&A.

​Who should join Founders, RA/QA leads and product teams at Indian medical device and IVD companies planning EU market entry, as well as advisors who support them.

​Speakers

• ​Leon Kobinger, Managing Director, CertHub

• ​Debraj Dasgupta, Managing Director, Inventicia GmbH (Host)

​About CertHub Europe's AI-powered regulatory compliance platform for medical device manufacturers (Munich, Germany).

​About Inventicia Basel-based partner supporting Indian MedTech companies on their way to the European market.