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
November 3-4: Menlo Park, CA
Early Bird Special: $695/person (register by 10/15/10)
Regular Price: $995 (registrations after 10/15/10)
Register for Seminar
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