This 3 course suite provides regulatory and quality professionals with a detailed review of international requirements for labeling medical devices.
The content of the courses within this suite are based on applicable laws, regulations and standards per the course specific country or region, and will provide you with detailed guidance supported by many examples on developing labeling for medical devices for your target market.
Upon completion of this suite, trainees will be able to correctly and successfully:
|Course Title Click on a title to view course description||ID||Duration|
|Labeling Requirements for Medical Devices in Europe||133||87|
|Electronic Instructions for Use for Medical Devices in the European Union||143||50|
|Labeling Requirements for Medical Devices in the US||144||70|