Newly Proposed Regulations for Drug-Device Combination Products Webinar

NEW REQUIREMENTS ARE HERE AND THERE'S MORE TO COME LATER IN THE YEAR

Get expert guidance on how to face these challenges pro-actively and efficiently so you can keep your development efforts on track and your marketed products on market.

Our industry experts will cover:

  • The new regulations for key markets including: the US (FDA), Europe (EMEA) and Japan (PDMA)
  • What has changed and where?
  • What your organization should be doing now and what to plan for.

Who should Attend

This Summit is specifically designed for C-Levels, Department Heads, Vice Presidents, Directors and Managers at pharmaceutical, biotechnology and medical device companies from the following departments:

  • Global Regulatory Affairs
  • Quality Assurance
  • Compliance
  • Clinical Operations
  • Clinical Affairs
  • R&D Operations
  • Medical Device Development
  • Pharmacovigilance
  • Drug Delivery