WORKSHOP PROGRAMME. Even early stage Life Science start-ups must be aware of the regulatory compliances needed to market a product . Are you part of a MedTech start-up developing medical equipment for diagnostic purposes, treatment, or disease prevention? Do you have sufficient knowledge about the regulatory laws and regulations applying to you? This unique program will provide you with baseline knowledge on regulatory compliance and give you access to workshops and local experts.
The regulatory journey is a programme giving you access to the necessary knowledge, tools, and feedback for regulatory compliance. The programme will provide detailed insight into the laws and regulations that your company and your product needs in order to enter the European market. The focus will be on medical device regulation (MDR), equipment for in vitro diagnostics (IVDR), and medical software. The programme is free of charge, but you must sign up here no later than September 7th…
Tuesday September 20th, 09.00- 16.00 to Wednesday November 23rd 2022
Kick-off workshop. Danish Life Science Cluster, COBIS, Ole Maaløes Vej 3, 2200, Copenhagen N.
MedTech start-ups developing medical equipment for diagnostic purposes, treatment, or disease prevention. Requirements to join the programme:
- Growth potential and ambitions
- Danish CPR-number
- Your business cannot be more than 5 years old