A guide for outsourcing medical writing for medical devices
Mapping medical device regulations
The implementation of the EU’s Medical Device Regulation (MDR) 2017/745 has been delayed, having had a scheduled date of 26 May 2020. Because of the Covid-19 pandemic and the...
The clinical evaluation report: document writing and compilation
Trilogy offers high-end medical writing that goes beyond just making sure a document is structured properly: it involves content-driven sanity checks, a sense of ownership of...
Strategic medical writing for device submissions
Julia Forjanic Klapproth of Trilogy Writing & Consulting explains why it is time to start using strategic medical writing in the world of device submissions.
Get the writing right
Gerry McGregor, a principal medical writer at Trilogy Writing & Consulting, explains how experienced medical writers can help medical device manufacturers meet the new regulatory...
