The success of a clinical development program depends on the proper documentation of research plans and results. Quintiles offers a range of flexible Medical Writing and Document Publishing solutions to support various clinical study documentation needs.
Our team of more than 70 writers have experience working in a broad range of indications and therapeutic areas. Located on five continents, Quintiles Global Medical Writing offers flexible solutions for single documents or an entire multi-study program.
Our Medical Writers can assist at any point in the product development lifecycle across Phase I to Phase IV, and have experience in a wide array of documents, including clinical study protocol development, Investigator Brochures, clinical study reports, patient narratives, DSMB updates, regulatory submissions and other documents involving study data. Our Medical Writing services follow ICH guidelines and are compatible with similar regulatory requirements.
Staff Publications and Presentations:
The Document Publishing team averages 15+ years plus experience and many are certified in several software applications used for electronic Publishing.
Experience You Can Trust:
Document and Submission Types:
Publishing services can be full publishing or submission-ready, as best meets the Sponsor’s needs. This allows the maximum flexibility and efficiency for the Sponsor. Quintiles can perform full publishing or submission-ready publishing as outlined below:
Expertise in medical writing for clinical research.
Senior Vice President and Global Head, Clinical Design & Reporting Services
Recent thinking: Data Integration and Partnerships
Vice President and Head, Clinical Analysis and Reporting Services
Vice President and Head of Global Regulatory Affairs