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PROFESSIONAL SERVICES

Consent Form Development

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

Flexible Process

We work with whatever materials you have ready to develop a compliant consent, even just a draft protocol.

Compliance and Clarity

Ensure regulatory compliance and participant comprehension with easy-to-understand consent forms developed by a team dedicated to consent best practices.

Accelerated Enrollment

Faster consent development and easy-to-understand content means enrollment activities takes less time.

Expert Guidance

Gain access to Advarra’s domain experts for precise and clear risk section development in addition to human subject protection expertise.

Quick Turnaround

Receive a complete consent form in days so you can stay on schedule.

Phase I and Early Phase

Approximately 75% of the consents we write are for phase I trials, and we understand early phase complexities and resource demands

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

Consent development turnaround times depend on accurate materials provided by the client. Any follow-up requiring a response may extend this turnaround time. 

How can Advarra’s Consent Development Services help save you time and ensure compliance?

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