Compliance

Pioneer Research conducts clinical research in accordance with FDA regulations, ICH Good Clinical Practice, and the requirements of the sponsors and institutional review boards overseeing our studies.

Institutional Biosafety Committee

Pioneer Research makes Institutional Biosafety Committee meeting minutes publicly available in accordance with the NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules.

IBC Meeting Minutes — March 17, 2026

Additional minutes are available on request at info@pioneerresearch.com.

Institutional Review Board Oversight

Every study conducted at Pioneer Research is reviewed and approved by an institutional review board before any participant is enrolled. The IRB reviews the protocol, the informed consent document, and any materials used to recruit participants, and provides continuing oversight for the life of the study.

Questions

info@pioneerresearch.com
(305) 420-5541