Services

MC Research

MC Research: Your Trusted Partner for Regulatory-Compliant Clinical Research Services in the Canadian Pharmaceutical and Biotech Industry

MC Research services include the following:
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Study Design & Planning

Study Design and Planning
We work with our clients to design and plan clinical studies that are scientifically rigorous, ethically sound, and feasible.
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Recruitment & Retention

Patient Recruitment and Retention
Our dedicated participant recruitment team employs diverse strategies, such as social media, advertising, and healthcare provider referrals, to identify and enroll eligible participants, while also emphasizing participant retention for study compliance and follow-up.
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Site Management & Monitoring

Site Management and Monitoring
Our experienced team offers comprehensive site management and monitoring services, ensuring protocol compliance, adherence to Good Clinical Practice principles, and regulatory requirements across various clinical trial phases and study types.
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site management and monitoring
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Data Management

Data Management and Analysis
We provide comprehensive data management and analysis services, ensuring accurate and high-quality data collection, analysis, and reporting in compliance with CDISC and STDM standards.
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About McResearch
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Regulatory Compliance

Regulatory Compliance
We provide guidance and support to ensure clinical trials comply with all relevant regulatory requirements, including those set by HC, FDA, EMA, and other regulatory bodies.
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Quality control & assurance

Quality control and assurance
Our comprehensive quality control and assurance program ensures that all clinical trials comply with Good Clinical Practice (GCP) guidelines and our internal quality standards.
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