<img height="1" width="1" style="display:none" src="https://www.facebook.com/tr?id=2179646889074564&amp;ev=PageView&amp;noscript=1">

Informed Consent Document Builder

The Informed Consent Builder Copilot rapidly creates an Informed Consent form that adheres to multiple regulatory bodies such as the US, EMEA, Australia, and New Zealand, and aligns with specific complex protocol requirements. Use Ryght’s template or upload your own.

Streamline Informed Consent Form Creation for Global Trials

Contract Research Organizations (CROs) and Sponsors understand the critical role informed consent forms (ICFs) play in clinical trials. But creating compliant, clear ICFs for multinational trials can be a time-consuming and error-prone process.

Traditionally, you'd adapt existing templates to each protocol, ensuring adherence to regulations across various countries.

Talk to Us
Informed Consent Document Builder Co-Pilot | Ryght
Informed Consent Document Builder Co-Pilot | Ryght

Ryght's Informed Consent Builder Copilot changes the game. This innovative tool simplifies and accelerates ICF creation, saving you valuable time and resources. Leverage Ryght's pre-built templates compliant with regulations in the US, EMEA, Australia, and New Zealand. Alternatively, upload your own templates for a seamless integration.

Explore the Ryght Platform

Ready to learn more?

Get in touch