Synchrogenix Information Strategies Synchrogenix partners with pharmaceutical, biotech, and medical device companies to develop documents for submission to regulatory agencies worldwide. We provide many of the benefits of in?house writers—including the experience and perspective of industry insiders—without the need to increase overhead or struggle with fluctuating workloads. Our writers and editors are permanent employees. So, unlike freelance writers, our team members can bring other Synchrogenix writers into the project if timelines or other dependencies change. Our additional value is that we have the experience to manage the writing activities so our client is able to focus on other important aspects of the project. Our regulatory writers and subject matter experts fit seamlessly and naturally into client teams because they come from various roles in the pharmaceutical industry, spanning all functional areas and dozens of therapeutic areas. These complementary backgrounds enable us to provide the holistic expertise necessary to create relevant submission-ready documents in nonclinical; clinical; chemistry, manufacturing, and controls, drug safety/pharmacovigilance; and regulatory strategy.