Global Medical Device Regulatory Requirements - Brazil (2 hours)
5
What you'll gain from this course
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Interactive modules and knowledge checks
Certificate available upon completion
This two-hour course provides a comprehensive overview of the regulatory requirements including the regulatory framework, pre- and post-market requirements, and the way Brazil is utilizing MDSAP.
Key learning objectives:
By the end of this course, you will be able to:
- Identify the legal and regulatory framework for medical devices in Brazil
- Determine the correct classification for medical devices
- Understand how Brazil utilizes MDSAP
- Understand the pre-market pathway(s) and requirements for medical devices in Brazil
- Understand the quality management system regulations required to market a medical device or IVD in Brazil
- Understand the post-market requirements for medical devices in Brazil
This course is essential for anyone wanting to bring a medical device or IVD to market into Brazil, and also for employees in regulatory, quality and compliance functions.
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