Create SOPs, WIs, and PDs, review CAPAs, Audit findings and provide resolutions.
Conduct periodic, independent reviews of essential documents to ensure audit readiness.
Creation of version-controlled source documents in accordance with the protocol. Our source documents include embedded protocol deviation checks within the worksheets to ensure compliance and accuracy.
With a combined experience of over 20 years, our team is highly skilled in identifying top-tier clinical research professionals with extensive expertise. You can be rest assured that you are receiving the best talent in the industry.
We are committed to increasing the diversity of Principal Investigators (PIs) and patient participation in clinical trials, starting with partnerships with clinicians of color.
Providing business opportunities, management support, visibility, and regulatory guidance to clinical research professionals at the site level.
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