Intertek (www.intertek.com)
 

Register for Medical Compliance in a Box Seminar and Webinar

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 

September 22-23: Minneapolis, MN, USAEarly Bird Special: $695/person (register by 9/3/10)
Regular Price: $995 (registrations after 9/3/10)
Register for Seminar
November 3-4: Menlo Park, CAEarly Bird Special: $695/person (register by 10/15/10)
Regular Price: $995 (registrations after 10/15/10)
Register for Seminar
Sneak Preview Webinar

Register for a free one-hour sneak preview webinar! The webinar is held on October 13. 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 and Regulatory: Use your Quality Management System 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 

Tuition includes a copy of the presentations 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
 

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