Medical device companies creating technical documentation, clinical / post-marketing reports, labeling and quality documentation with increasing regulations and recent MDR/IVDR compliance in mind …
Commercialization of new drugsrequire careful navigation through complex regulations defined by Global health authorities. Drug development process needs extensive collaborations with internal &am…
In order to scale, you must reuse content; To reuse content, you must standardize content; To create standardized content, you must develop standards that all content creators adhere to
Why Bes…
Constant Global regulatory changes and more recently EU MDR and In Vitro Diagnostic Regulations are compounding “content” requirements. Structuring content can help medical device manufacturers im…
Areyou “ready” to move to 100% structured content? If not, see how you can be fully in MS Word (linking easily to structured content) OR stay Hybrid and still take advantages of Structured compone…
