Description
Ethics/IRB Application Support | Navigate Ethical Approval
Assistance with IRB and ethics committee applications. We help you prepare compelling, complete applications that address committee concerns proactively — from the protocol and informed consent form to the data management plan and your responses to committee queries.
Service Details
| Turnaround | Standard: 5-7 business days |
| Best for | Researchers preparing an application to an IRB or ethics committee |
Support Includes
- Protocol document preparation
- Informed consent form drafting
- Risk-benefit analysis articulation
- Data management plan
- Recruitment material review
- Response to committee queries
How It Works
- Send us your study details, any draft documents, and your committee’s application requirements
- We prepare your application documents and review your recruitment materials
- You review the drafts, and we revise based on your feedback
- If the committee comes back with queries, we help you prepare your response
Which Service Do You Need?
If your study design is not settled yet, start with Study Design Consultation, which covers design selection, sample size, outcomes, and bias mitigation. If you need a complete clinical trial protocol developed from concept to final document, see Clinical Protocol Development.
Frequently Asked Questions
Which documents do you help prepare?
The protocol document, the informed consent form, the risk-benefit analysis, and the data management plan. We also review your recruitment materials.
Do you help after the application is submitted?
Yes. Support includes responding to committee queries.
How long does it take?
Standard turnaround is 5-7 business days.
Get started: add this service to your cart, or email co*****@*******se.com with your study details if you have questions first.
