Case Study

Large Clinical Research Site Network Streamlines Study Startup with Reliable, Timely ICF Writing Services

Developing informed consent forms (ICFs) for clinical research requires an understanding of the protocol, an understanding of the regulations, and time to ensure compliance and clarity.

A large clinical research site network needed a new ICF writing partner when their regular vendor discontinued offering the service. In this case study, find out how Advarra: 

  • Delivered a compliant and easy to understand ICF in as little as 2 business days
  • Created a reliable and flexible processes
  • Delivered excellent support to ensure needs were met

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Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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