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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.
- 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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Who Should Watch?
Certificate of Attendance
Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour