The Importance of Migrating to DITA for Medical Device Documentation

In the medical device industry, the stakes for accurate and up-to-date technical documentation are exceptionally high. Manuals, safety instructions, installation guides, and other forms of documentation are not just user resources—they are critical to regulatory compliance with the FDA (Food and Drug Administration), EMA (European Medicines Agency), and ISO (International Organization for Standardization).

Read more: https://blog.metapercept.com/highlight-single/the-importance-of-migrating-to-dita-for-medical-device-documentation