Due to recent changes to regulatory requirements - including ISO 13485, the Medical Device Directive, and IEC 60601-1 - medical device manufacturers are now required to have a documented risk management system in place. Rest assured, implementing basic risk management principles doesn't have to be a complex task. Learn the simple steps you can take towards compliance by watching Intertek's recorded webinar. In just 45 minutes, you'll learn:

• The basic principles of ISO 14971:2007, and how they are related to other medical device directives and regulations
• How risk management can be implemented in conjunction with a quality management system
• How to include risk management as an integral part of the design, production, and post-production processes
• How to demonstrate a clear understanding of the potential hazards to the end user

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Our Discount Policy

1. You will be given a 10% discount on our published course fee when registering 90 calendar days prior to the start date of the training course or paid webinar.
2. For 3 or more people from the same company (identified by the same company name) attending one training course or one paid webinar, each participant will enjoy 10% discount on our published course fee.
3. Maximum 20% discount will be granted to an attendee if both conditions #1 and #2 are satisfied.

Please note: This discount policy only applies to Intertek’s public training courses or publicly held paid webinars and is not applicable to any on-site training course or paid webinar offered to a specific company.