Our webinars
In our open webinars, our experts will present our solutions to you live with no obligation.
MDR and Go-To-Market for start-ups – digitally simplify the approval process with Themis
Do you want to bring your medical device to market quickly, efficiently and compliantly?
Then our focus webinar especially for start-ups in the medtech sector is just right for you.
Find out how you can use BAYOOSOFT Themis to digitize the approval process in accordance with the Medical Device Regulation (MDR) – and thus save time, reduce regulatory hurdles and strategically accelerate your market launch.
Our experts will show you how Themis can support you with specific application examples:
- structured and comprehensible documentation
- efficient risk management
- Targeted preparation for audits and notified bodies
Make your approval strategy fit for the MDR – and gain practical knowledge in 45 minutes that you can implement directly.
