Are you seeking complete insights into navigating the European regulatory landscape for MedTech products? Look no further! Join our exclusive short course adapted for C-level management, focusing on MDR/IVDR implementation and resource and budget allocation.

📚 Course Title: 𝗦𝗵𝗼𝗿𝘁 𝗖𝗼𝘂𝗿𝘀𝗲 𝗼𝗻 𝘁𝗵𝗲 𝗧𝗿𝗮𝗶𝗻𝗶𝗻𝗴 𝗳𝗼𝗿 𝗖-𝗟𝗲𝘃𝗲𝗹 𝗠𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁 𝗼𝗳 𝗠𝗮𝗿𝗸𝗲𝘁 𝗢𝗽𝗲𝗿𝗮𝘁𝗼𝗿𝘀 𝗼𝗻 𝗠𝗗𝗥/𝗜𝗩𝗗𝗥 𝗜𝗺𝗽𝗹𝗲𝗺𝗲𝗻𝘁𝗮𝘁𝗶𝗼𝗻 𝗮𝗻𝗱 𝗥𝗲𝘀𝗼𝘂𝗿𝗰𝗲 𝗔𝗹𝗹𝗼𝗰𝗮𝘁𝗶𝗼𝗻

Sessions:
🗓️17 May 2024: Face-to-Face Session - Learn how to successfully market your MedTech product in today’s highly regulatory European landscape.
🗓️24 May 2024: Webinar - Understand the investments needed to bridge the “regulatory valley of death” in Europe.
🗓️31 May 2024: Webinar - Gain insights into selecting the right Notified Body for your innovative MedTech product.
🗓️7 June 2024: Webinar - Discover strategies for developing and implementing an effective quality management system and technical documentation.
🗓️14 June 2024: Webinar - Learn from a best practice case of a start-up company that invests at the right time.
🗓️21 June 2024: Face-to-Face Session - Exchange challenges, opportunities, and experiences within the highly regulated European landscape.

Don’t miss this unique opportunity to equip yourself with the knowledge and strategies necessary to navigate the complex European regulatory environment.
Secure your place today and elevate your organization’s success in the MedTech industry!

For more details and to REGISTER, click the link below!
📝🔗 https://nobocap.eu/2024/04/05/short-course-on-training-for-c-level-mana…

NoBoCap project is co-funded by European Union through EU4Health programme.