International Product Registration: What documents are required? 2015

  • 17 Jun 2015
  • Webinar

Description

International Product Registration: What documents are required? 2015 is an event dedicated to international product registration for IVDs & Medical Devices.

Topics
  • Role and responsibilities of US manufacturers & in-country distributors
  • International regulation- Overview of country by country differences
  • Working with in-country distributors
  • Identifying the key players
  • Types of documents need
  • Sales forecasting – Who needs to know?
  • Best practices for document legalizations
  • Medical Device & IVDs
  • How to get documents embassy legalized
  • Apostille vs. Authentications
  • Pitfalls – What to look out for
Who should Attend
  • Product Managers
  • Regulatory Affairs Specialist/Managers
  • Administrative Professionals working in Regulatory
  • Marketing Professionals

Past Events

Important

Please, check "International Product Registration: What documents are required?" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device

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