Clarity and transparency in regulatory documents.

In clinical development, medical communication is critical to support the regulatory success of your product. You need to translate the complexity of your trial into clear documentation for your molecule or medical device.
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Optimize your product approval path

As a global provider of medical writing services, IQVIA offers a range of high quality, flexible, and timely medical writing solutions to support your entire program needs.
  • Product development plans
  • Clinical study protocols
  • Clinical study reports
  • Patient narratives
  • Investigator brochures

The transparency you need

As requirements for clinical trial disclosures continue to increase, IQVIA has a suite of clinical trial disclosure services, from consulting to postings and anonymization, including Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE).
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