Our Services
CRO Consulting Inc., is a boutique clinical research organization that provides clinical and regulatory landscape strategic expertise to small and medium size companies for pharmaceutical, medical devices, AI software medical devices, prescription digital therapeutics, and in-vitro diagnostics solutions for human and animal health industries.
We have expertise in developing and executing industry sponsored clinical trials, investigator-initiated clinical trials, and government funded clinical trials from early development to post-market studies globally.
We maintain excellent working relationships with external collaborators, including clinical sites, principal investigators, CROs, data management, federal agencies (e.g., NIH, BARDA), and reference laboratories to develop more efficient and cost-effective clinical trials that meet your company’s goals.
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Clinical study oversight and management.
EDC and IRB support.
4 team meetings a month.
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Study oversight and management.
EDC and IRB support.
Clinical study documents preparation and review. it includes study protocol, protocol amendments, consent forms and CRF revisions.
Project management, if requested.
Study budget review and invoice approval, if requested.
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Clinical operations, data management, regulatory and monitoring support.