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.
Register for Webinar

Seminar Topics

A panel of Intertek experts will introduce you to the regulations and opportunities that occur throughout the medical device product life cycle, including:

• Quality Management Systems: Use your QMS to demonstrate your ability to provide medical devices that consistently meet customer and regulatory requirements
• Product Safety and Electromagnetic Compatibility (EMC): Ensure that your device poses no hazard to the patient or end user
• Product Performance: Determine how well and how long your device will last, so you can pre-empt service issues and avoid performance-based recalls
• Environmental Compliance: Ensure your product's compliance with restricted substance, waste disposal/recycling, energy usage, and other regulations
• FDA 510(k) Reviews: Learn how working with an expert 510(k) reviewer can significantly shorten your total submission process

Seminar Registration

Registration is only $1,095 per person. Tuition includes all course manuals and reference materials, and lunches and refreshment breaks on both days. You'll also receive a certificate for 1.4 CEUs - credits which may be applied towards your continuing education or training requirements.

Who should attend?

• Quality managers
• RA managers
• Start-up companies
• Companies wanting to expand into new markets

Learn more about our Medical Device Testing Services