IRB-Tailored Documents - Kinetiq
Review-Ready Documents to Move Your Research Forward
Our consultants have decades of research experience in exciting fields from international research, to biobanking and tissue procurement, to laboratory assays and in vitro diagnostics, to healthcare software applications, to social-behavioral studies, to investigator-initiated research, and they will deliver ready-to-review documents to fit your needs.
Experts with direct experience in research plan development and IRB review work with your organization to craft a protocol that fits your business needs. The Kinetiq protocol development team delivers scientifically sound, regulatorily compliant protocols that are ready to present to any IRB.
Go beyond the protocol.
The Kinetiq medical writing team offers a full suite of IRB-tailored clinical trial documents and services, including: recruitment materials, consent forms, grants, investigator brochures, and device manuals. We also develop educational websites and brochures.
Managing Director, Regulatory Consulting
An experienced regulatory and research attorney.Request Service Info