ENVIRONMENTAL MANAGEMENT SERVICES

• Are you manufacturing, importing or supplying medical devices in Europe?
• Do these include electrical/electronic devices?
• Are you up-to-date with the latest implications of the EU RoHS Directive?
• Do you understand the packaging and packaging waste regulations?
• Have you registered with EU countries if you provide batteries in your products?
• Are you aware of the European restrictions on manufacture/import of chemicals which took effect in 2009?
• Would compliance with EN ISO 14001 or the EU Eco-label program help your marketing?

There is an ever-increasing portfolio of European environmental legislation which applies to medical device companies, ranging from importation of raw materials to end-of-life device disposal. Thus a complete understanding of these issues is important, not only to European manufacturers, but also to non-European companies that export to Europe.

Based upon knowledge of the associated voluntary standards and eco-friendly labeling programs, Donawa Lifescience Consulting can provide advice to medical device companies on:

• Packaging directives and standards (more)
• Electronic waste directive (more)
• Hazardous substances (more)
• EU chemical manufacture and importation (more)
• EU Batteries Directive (more)
• ISO 14001 compliance (more)
• Environmentally conscious design (more)
• Eco-labeling (more)

If you have an environment-related question, contact us to speak with our Environmental Systems Specialist, who is a recognized expert in this area.