In bringing together for you our network of experts with deep specialist knowledge and experience, we offer a full range of medical and scientific writing services to support your products through the entire lifecycle. We offer a choice of flexible delivery models to suit your needs, on both large and small scale, including time and materials, deliverable, or unit-based pricing, and FSP staff augmentation models, with the option to combine with other IQVIA services.
Create transparency in your regulatory documents with a range of medical writing services that deliver quality and timeliness throughout your product development lifecycle.
Improve the performance of your clinical trials with the power of the IQVIA CORE.
Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.
Explore our end-to-end, full service clinical development capabilities including Therapeutics expertise, Development Planning, Phase I early clinical development, Phase IIb/III and Phase IV Trials, Regulatory Submission and Post-Launch Studies.
