Effective Medical Device Standards Monitoring

Global standards change regularly. To read or analyze larger documents, translating any non-English regulations is a time consuming process. In addition, some countries do not provide detailed standards and interpreting such short documents need deeper analyzing capacity.

To accomplish this, we include these 3 areas:

Standards monitoring (you can opt for alerts that are manually vetted by our analysts and set a frequency on how often you prefer to receive) and share (individual alerts or group few and convert to a newsletter and share to other stake holders using built-in newsletter functionality)
Standards documents repository search

Standards Monitoring – Be proactive

To accomplish this, we include these 3 areas:

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Regulatory Requirements Database

Regulatory Impact Assessment (RIA)

Products

Resources

Company