MC Research: Your Trusted Partner for Regulatory-Compliant Clinical Research Services in the Canadian Pharmaceutical and Biotech Industry.
Our team of experienced professionals has expertise in conducting clinical trials across various therapeutic areas, including oncology, neurology, cardiology, and more. MC Research Services Include the following:
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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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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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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