Medical writing today is much more than entering data onto a page. With the ever-increasing demand to bring new drugs to market as quickly as possible, the ability to write easily understood clinical study documents is a growing priority for sponsor companies. Urtech Medical Writing specializes in satisfying the growing need for submission-ready, ICH-compliant documents. Behind Urtech Medical Writing is Thomas J Purcell, a freelance medical writer with 25 years of experience in writing, editing, and proofreading a wide variety of clinical and regulatory documents. He understands the importance of accurate medical writing as a critical component to the clinical development process. Whether your medical writing needs include study protocols, clinical study reports, Investigator's Brochures, or clinical sections of regulatory submissions such as annual reports, briefing packages, or New Drug Applications, Urtech will write your clinical regulatory documents and ensure that documents are completed according to your standards and to your processes--on time and within budget.