RoHS2 Compliance for Medical Devices 2014 is a webinar dedicated to Restriction of Hazardous Substances (RoHS) 2 directive and its compliance, including:
- Who advise and assess on RoHS 2 medical device exemptions for the European Commission and how and where exemptions exist and what is the application & exemption submission process
- Are your products in scope of the RoHS 2 directive and what the consequences may be if you are not compliant
- Achieving compliance with RoHS2
Who should Attend
Representatives from medical device companies, including Vice- Presidents, Directors, Managers of:
- Quality Assurance
- Regulatory Affairs
- Environmental Sustainability
- Quality Affairs
- Ecodesign
- Environmental Compliance
- Product Component Sourcing
- Manufacturing Operations
- Materials & Design
