W WCG IRB

Non-downloadable software for use by clinical researchers, research sponsors and clinical research organizations for use in automating the submission, review and approval process of human subject clinical research projects

Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the human subjects of research; providing regulatory compliance consultation services in the nature of advice concerning due diligence, strategic development, and regulatory policy in the field of clinical trials involving human subjects; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects