Medical device manufacturers must consider safety from many perspectives. Learn about the specific regulatory requirements for the North American market.

Certification is a critical component in the healthcare industry due to the risks medical products could pose to patients and healthcare providers. Hence, healthcare device manufacturers must consider safety from many aspects, such as usability, electrical safety, risk management, environmental, software integration, and more. The regulatory environment varies, and there are differences between world markets. This webinar covers the specific regulatory requirements for the North American market.

Watch the webinar to learn about:

• The regulatory environments in the US and Canada
• North American legal requirements
• The US vs. Canada – differences in the product approval process

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