Medical Device Regulation MasterClass - US edition

The course is very interactive: In Break-Out Groups we will review many examples covering borderline classification products and reports for the market surveillance.

08-09 February, 2024, Virtual

Time Zone: Eastern Standard Time (EST) - UTC−05:00

Overview

This course give you an overall and complete overview about the requirements of the Global Medical Device Regulation. We will discuss the basics about risk classification systems, about the requirements for conformity assessment procedures, about clinical evaluations and trials and about regulatory challenges. The course is very interactive: In Break-Out Groups we will review many examples covering borderline classification products and reports for the market surveillance. Overall you will broaden your experiences in a workshop by exchange with colleagues all over the world.

#masterclass     #glceurope      #pharma      #globaltraining       #MedicalDevice    #MedicalDeviceRegulation

RECOMMENDATION

Who should attend?

• QA Professionals
• Regulatory Affairs Manager
• Officials from Authorities
• Manufacturing Experts
• Pharmacovigilance Experts
• For beginners and advanced

Event Sponsor

Esko is a global provider of integrated software and hardware solutions that accelerate the go-to-market process of packaged goods. Our products empower teams to support and manage the packaging design and print processes for brand owners, retailers, pre-media and trade shops, manufacturers, and converters. 

 To learn more visit : https://www.esko.com/