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Expert Clinical Research Services

Providing high-quality, independent clinical trial monitoring services in Atlantic Canada and Québec.

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About ACM

Who We Are

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Atlantic Clinical Monitoring (ACM) is an independent clinical trial monitoring organization dedicated to supporting high-quality, compliant, and efficient clinical research. We provide experienced Good Clinical Practice (GCP) monitoring services to academic institutions, and biotechnology companies across Atlantic Canada and Québec. Our monitors work collaboratively with sponsors and study sites to ensure participant safety, data integrity, and regulatory compliance throughout every stage of a clinical trial.

At ACM, we combine the rigor of industry standards with a deep understanding of the academic and clinical practice research environments. Our team brings extensive experience in Phase I–IV clinical trials across a broad range of vaccines/infectious diseases, delivering practical, responsive, and risk-based monitoring solutions tailored to each study.

Whether supporting emerging biotech companies, investigator-initiated research, or multi-site clinical trials, we are committed to advancing clinical research through quality, integrity, and trusted partnerships.

What We Offer

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What We Do

Our Services

Site Monitoring

Independent monitoring services that ensure your clinical trial is conducted in accordance with ICH-GCP, the study protocol, and applicable regulatory requirements. Our monitors provide routine site visits, source data verification, risk-based monitoring, issue management, and comprehensive monitoring reports.

Quality Management & SOP Development

Develop and strengthen your quality framework with customized Standard Operating Procedures (SOPs), Quality Management Systems (QMS), monitoring plans, and study-specific documentation. We help establish practical, compliant processes that support high-quality clinical research.

Audits & Quality Oversight

Maintain confidence in your trial through independent quality oversight. We conduct internal audits, site assessments, process reviews, CAPA follow-up, and ongoing quality evaluations to identify risks early and support continuous improvement.

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Our Team

Our team brings decades of experience in clinical trial monitoring, quality management, and research operations. With expertise spanning academic, industry-sponsored, and investigator-initiated studies, we are committed to delivering independent, high-quality oversight that supports participant safety, data integrity, and regulatory compliance.

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Dr. Scott Halperin
Chair, Board of Directors

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Allison Young
Chief Executive Officer

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James Makonyere
Treasurer

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Belinda Grouchy
Clinical Research Associate

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Pamela MacIntyre
Clinical Research Associate

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