Illuminated Research® provides consulting and medical writing services related to the preparation of prestudy clinical materials, the development of poststudy regulatory submission documents, and the production of scientific publications. In particular, Illuminated Research specializes in drafting briefing packets, clinical study reports, and clinical sections of submission dossiers associated with pharmaceutical drugs and devices.
Illuminated Research produces detail-oriented documents which are informed by a strong knowledge of regulatory guidelines, the expertise gained through authorship of materials across multiple therapeutic areas, and the experience obtained from direct participation in research studies. In particular, our medical writers have advanced degrees and past experiences in the laboratory, as well as in the field, having served (variously) in the roles of benchtop researcher, clinical study coordinator, clinical study monitor, and clinical study manager.
Illuminated Research is dedicated to meeting client needs through communication, adherence to project milestones, and careful preparation of quality documents. Illuminated Research is focused on assisting our clients with the successful submission of dossiers to regulatory agencies, the development of complex messaging, and the ethical presentation of scientific results obtained in clinical research studies.