Intertek's "Medical Compliance In A Box" seminars are informative two-day seminars that will help you navigate the market-entry requirements for your medical device in North America and the European Union.
2010 Seminar Dates and Locations:
March 17 – 18: Lake Forest, CA, USA
May 12 – 13: Toronto, ON, Canada
June 29 - 30: Boxborough, MA, USA
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Sneak Preview Webinar
Register for a free one-hour sneak preview webinar! The webinars are held on April 20 and June 8. This webinar is presented by a panel of Intertek experts who will introduce you to the regulations and opportunities that occur throughout the medical device product life cycle.
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Are Your Medical Device Products Compliant?
A review of new and upcoming materials restrictions and environmental requirements for medical devices
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Green Convergence: A Global Regulatory Update Webinar
Intertek will provide a review of current and future environmental requirements
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Is your Company prepared to meet the Biofuels Sustainability requirements?
A Free Intertek Presentation
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Is Your Product Really Green?
A review of the requirements for green marketing claims
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Are You Ready for the January 2010 Changes to the REACH SVHC Candidate List?
A Free REACH Webinar
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Are California’s green product requirements creating a confusing challenge for your business?
A review of the current and upcoming environmental regulations for products sold in California
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Are you Aware of Walmart’s RoHS Certification Program?
A review of the program requirements, applicable product categories, and approaches to compliance
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Restricted and Declarable Substance Management: REACH, RoHS and Beyond ...
A joint webinar from Intertek and ENVIRON
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Is a Joint Dossier the Right Solution for Your Company?
A review of the process of joint dossier submission for REACH Registration
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Is There Any Protection Against Counterfeit Products?
A review of testing and identification methods for counterfeit products
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Imminent Global Health and Environmental Requirements: How can Middle Eastern companies implement a sound compliance strategy?
A Restricted Substances Webinar
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Future Proofing Your REACH SVHC Testing
Process for testing once and guarding against the future
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Need a REACH Dossier?
A review of Intertek’s available REACH dossiers and overall dossier process
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Does your product meet the new EuP Directive?
An Online EuP Seminar
• Date: Tuesday, March 10, 2009
• Time: 2:30 pm EST
• Duration: 1 hour
• Cost: Free
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REACH Registration: Budgeting and Completing
A review of the steps to completing REACH Registration from a business perspective
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The Greening of Electronics in a Global Economy
Intertek – California DTSC Symposium
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What Will the Revised RoHS and WEEE Potentially Look Like?
A review of the proposed revisions to the RoHS and WEEE Directives
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RoHS, REACH, WEEE, Oh My!
Checklist for materials restrictions and recycling requirements for electronics being sold into the EU
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I’ve Pre-Registered for REACH. What’s next?
Considerations for REACH dossier creation
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If my suppliers are registering for REACH, do I still have responsibilities?
Rules and options for REACH compliance using Only Representatives in global supply chain management
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What do you mean my “product’s packaging is non-compliant?"
Materials restrictions and recycling requirements for product packaging and batteries
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More material declaration requirements from the EU?
REACH Substances of Very High Concern (SVHC) declaration and testing requirements for products
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What will the new RoHS look like?
Expected changes and updates to the RoHS Directive
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The Pros and Cons of REACH Only Representation
Options and Industry Trends
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Why are Medical Device Companies Converting to RoHS Compliance?
An Online RoHS Webinar
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Korea RoHS: Are You Ready?
Differences from EU RoHS, WEEE, and ELV and immediate requirements for January 1, 2008
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REACH Beyond Borders
What North American chemical exporters and manufacturers need to know about the European Chemical Directive
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Request more information to see how Intertek can help your organization with Health and Environmental Events.