About Us

Synchronizing Strategy and Information

Synchrogenix partners with pharmaceutical and biotech companies to develop submission documents for global regulatory agencies.

Since 1986, our core competency at Synchrogenix has been regulatory writing for the pharmaceutical and biotech industry. Focusing in this crucial aspect of the drug development process has allowed us to hone our unique methodology and build a team of regulatory writers who are experts and thought leaders in the field.

Rather than vertically specializing in a functional area, as a CRO, CMO, or contract lab might do, Synchrogenix horizontally bridges all functional areas within drug development. Our strength is integrating with key stakeholders to create submission documents that are comprehensive, concise, and clear, as well as consistent within and across the entire submission. Synchrogenix breaks through silos, uniting many single elements into one story...your story.

Read more about Our Team and our Methodology.