Create clarity and transparency for your clinical programs

In clinical development, what you say — and how you say it — has never mattered more. "Transparency” is now the industry buzzword. Requirements for clinical trial disclosures continue to increase: regulatory updates, mandatory registries, expanding disclosure data, including the transparency initiatives announced by the EMA1, EFPIA2, and PhRMA3.

IQVIA offers a range of flexible medical writing and document publishing solutions to support many types of study needs, giving you the quality and timeliness that can keep your project on track.

  • Our Global Medical Writing team offers flexible solutions from single documents to an entire multi-study program, at any point in the product development lifecycle across Phase I to Phase IV.
  • Deep writing experience in clinical study protocol development, investigator brochures, clinical study reports, patient narratives, DSMB updates, regulatory submissions, and disclosure delivers what you need, and how you need it.
  • Our Document Publishing teams are certified in several software applications used for electronic publishing, providing full or submission-ready publishing services.

The success of your clinical program could depend on how you document it. IQVIA can help.

Find out how our medical writing and document publishing services could work for you.

Data Extraction and Management
Access a foundation of relevant real-world data.