Medical Writing

Quality and clarity are vital when producing any regulatory document. Partnering with experienced medical writers can help accelerate the approval process and avoid costly delays. At Premier Research, our dedicated medical writers work as a true extension of your team.

Averaging 20 years of industry experience, our writers share a passion for excellence. All have strong analytical communication skills and expertise across multiple therapeutic areas, including analgesia, oncology, pediatrics, cardiology, neurology, dermatology, gastroenterology, endocrinology, immunology, psychiatry, ophthalmology, rare diseases, rheumatology, and medical devices.

Our writers have thorough knowledge of U.S. Food and Drug Administration and European Medicines Agency guidelines. In addition, each has extensive experience in the development of study protocols, investigator brochures, patient-facing documents, clinical study reports (CSRs), patient narratives, and other regulatory submission documents. We also keep our finger on the pulse of industry standards and employ the principles of CORE Reference, focused authoring, and TransCelerate’s common document templates.

When you engage with Premier Research medical writers, you can count on timely, high-quality deliverables from a team recognized for its exemplary work and extraordinary levels of customer satisfaction.