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.
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.
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