Protecting participants from any potential risk is the central focus of the IRB approval process. As a doctoral candidate, you’re responsible for clearly outlining these safeguards, which can feel overwhelming. Fortunately, we’ve guided many clients through this process, and we’re here to ensure your IRB application is comprehensive and ready for approval.
Complete and Accurate IRB Applications
Preparing a full, accurate IRB application is essential to avoid delays and gain approval. We walk you through each section, ensuring your application covers all necessary details—especially those related to participant safety, anonymity, and confidentiality. With our guidance, you can feel assured that your application reflects the high level of ethical consideration expected by the IRB.
Designing Ethical Research Protocols
Whether your study is qualitative or quantitative, clear, ethical research protocols are key. We work with you to create protocols for each phase, from informed consent to data collection and handling. If unexpected situations arise during data collection, you’ll be prepared to address them responsibly and in alignment with IRB standards.
Ready for IRB Approval?
You don’t have to face the IRB process alone. With our expertise and personalized support, your IRB application will demonstrate thorough planning and a commitment to participant protection—moving you one step closer to approval and research success.
