PROFESSIONAL SERVICES
Consent Form Development
Ensure fast, compliant, and easy-to-read informed consent forms (ICFs) with Advarra’s expert Consent Development Services. Whether you’re in early phase research or managing complex clinical trials, our specialized team delivers IRB-ready consents to help you save time, streamline operations, and meet regulatory requirements – without needing to use Advarra’s IRB.
Key Offerings
- Consent materials written in 3-5 days
- Save time and optimize compliance with comprehensive, easy-to-read informed consent forms (ICFs) written by IRB experts.
- For every type of trial in every phase, our specialized team delivers IRB-ready consents to help streamline operations, speed enrollment, and meet regulatory requirements.
- Minor assent and parental permissions
- Sub-study and ancillary consents
- Phase I-IV support
Consent Development Services for Every Project
Turnaround Times
We’re your secret weapon to writing compliant consent forms faster.
3-5 business days or less from submission to consent provided to client.
3-5 business
days
days
Consent development turnaround times depend on accurate materials provided by the client. Any follow-up requiring a response may extend this turnaround time.