Regulations for Medical Device Development Workshop: Dive into the key regulatory requirements governing medical device development across global markets.
Learning Objectives
- Learn key regulations affecting medical device development.
- Understand regulatory pathways and approval processes.
- Develop skills to create compliant technical documentation.
- Ensure product safety and regulatory adherence.
- Improve development processes to meet regulatory standards.
Framework Connections
The materials within this course focus on the NICE Framework Task, Knowledge, and Skill statements identified within the indicated NICE Framework component(s):
Competency Areas
Feedback
If you would like to provide feedback on this course, please e-mail the NICCS team at NICCS@mail.cisa.dhs.gov. Please keep in mind that NICCS does not own this course or accept payment for course entry. If you have questions related to the details of this course, such as cost, prerequisites, how to register, etc., please contact the course training provider directly. You can find course training provider contact information by following the link that says “Visit course page for more information...” on this page.