Services

We are a next-generation clinical research consultancy, dedicated to transforming the way clinical trials are conducted. With deep expertise in site management, third-party audits, monitoring, and regulatory compliance, we help sponsors, CROs, and biotech companies achieve operational excellence, regulatory readiness, and high-quality outcomes. We are driven by innovation, integrity, and precision, combining technology-enabled workflows, expert teams, and robust quality systems to deliver efficient, compliant, and patient-focused solutions.

Site Management Services (AQSITE)

AQSite delivers end-to-end site management support from feasibility to close-out ensuring every study is conducted with operational precision, ethical oversight, and patient-centric focus. Our expertise bridges sponsors, investigators, and participants to drive trial success.

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Third-party Audit Services (AQSURE)

AQSure delivers end-to-end audit support—including CRO, BA/BE, vendor, and regulatory audits with a focus on uncovering gaps, mitigating risks, and enhancing operational efficiency. Our experienced auditors provide actionable insights that strengthen compliance and process quality..

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Trial Monitoring Services (AQ360)

AQ360 provides specialized third-party monitoring services for clinical trials of all phases, delivering transparent oversight and enhanced operational control. Our expert monitors ensure strict protocol adherence, robust data quality, and patient safety, while proactively identifying potential risks and resolving issues before they impact study timelines. Sponsors benefit from actionable insights, consistent site performance, and reliable progress tracking, enabling confident decision-making and successful trial outcomes.

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Regulatory Compliance Services (AQREGX)

From pre-inspection readiness to regulatory query management, AQRegX ensures smooth audits and consistent adherence to guidelines.

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