Medical Writing Medical Writing

Medical writing is an integral part of all phase I-IV clinical research. The progression of compound in the development process hinges on the data obtained from clinical trials and its accurate presentation and interpretation.

The manner in which a protocol is put together is equally important to the data produced and how it is presented, as it dictates the way a study will be conducted. Richmond Pharmacology’s Medical Writing Department has considerable experience in producing Clinical Study Protocols and Study Reports according to ICH guidelines. Each protocol is developed in collaboration with the Sponsor in order to fulfil Sponsor requirements and objectives. All protocols are written by Richmond’s medical writing team, with input from Richmond’s medical team including the Medical Director.

The Clinical Study Report is the final deliverable and the one document for which the study will be remembered. Our experienced Medical Writing Department works alongside the clinical, data management and statistical analysis team throughout the study to ensure accurate representation of data and results of the clinical study.

All of our reports are written to ICH guidelines and undergo a full process of comment integration, QC and review. Richmond Pharmacology can use its standard templates or those of the sponsor company. Each study report, both interim and final have input from Richmond Pharmacology’s experienced medical team including input from Richmond’s Medical Director, ensuring your study reports are given attention most other medical writing providers are unable to offer.

Case studies

The thorough approach to QTc studies ("Your perfect partner for conducting definitive thorough QT studies, all under one roof")

Timelines, Tight Timelines and Even Tighter Timelines in a Phase I Environment (We know we can help your business. We always rise to the challenge)