Medical Device Market Access MasterClass - EU edition

Join us for a dynamic four-session training program designed to equip participants with the knowledge and skills needed to excel in pharmaceutical market access.
 

06-07 February, 2025, Virtual

Time Zone: UTC/GMT+1 /CET

Overview

 
Welcome to the Medical Device Market Access Masterclass - EU Edition, a comprehensive and advanced program designed to equip you with the critical skills and knowledge necessary to navigate the complexities of market access in the European Union. This masterclass will delve into the intricate details of the EU Medical Device Regulation (MDR), providing you with strategic insights to successfully bring your products to market. Through expert-led sessions, you will explore the latest regulatory updates, economic operator roles, and best practices for compliance and market entry. Our interactive workshop and case studies will enable you to apply these strategies in real-world scenarios, ensuring you leave with actionable knowledge to accelerate your market access efforts. Join a global network of professionals and elevate your expertise in EU medical device regulations.

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RECOMMENDATION

Who should attend?

-Regulatory Affairs Professionals focused on EU market entry
-Quality Assurance Managers responsible for compliance with EU regulations
-Market Access Specialists aiming to navigate the EU medical device landscape
-Medical Device Developers and Engineers seeking to understand EU-specific requirements
-Compliance Officers and Legal Experts advising on MDR and post-market surveillance
-Business Development and Product Managers planning market expansion in the EU
-Consultants and Advisors specializing in medical device regulation and market access