Full-Service CRO · Global

MetaPharm Clinical Research

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Projects

Subjects

Countries

Years of Experience

Services

End-to-end clinical development capabilities

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Strategic Development

Maximize your product’s potential with expertise that reduces delays and costs across every clinical step.

Clinical Operations

End-to-end study conduct with dedicated project management, site networks, and quality monitoring.

Medical Writing

Regulatory-ready documentation from protocols and IBs to CSRs and submission packages.

Data Management

High-quality clinical data powered by industry platforms including Medidata Rave.

Biostatistics & SAS®

Scientifically accurate, validated, and reproducible statistical results across therapeutic areas.

Safety Management

Pharmacovigilance and safety monitoring focused on patient protection and regulatory compliance.

Quality & Training

Quality systems, SOP alignment, and training that keep trials inspection-ready.

Regulatory Affairs

Regulatory strategy and submission support for FDA, Health Canada, and EU pathways.

How we work

A clear clinical workflow from design to submission

Design

Build

Conduct

Analyze

Submit

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Expertise

Therapeutic depth across priority indications

Pain

Specialized trial strategies for acute and chronic pain programs with rigorous endpoint control.

Women's Health

Dedicated operational support for women’s health indications across development phases.

Respiratory

Respiratory and allergy trial expertise focused on on-time, on-budget enrollment.

Neurology

CNS expertise spanning rating instruments, eCOA, and hard-to-recruit indications.

Infectious Diseases

Full-service infectious disease development with site proximity and agile pandemic-ready processes.

Men's Health

Focused clinical operations for men’s health indications with quality-driven delivery.

Technology

Validated platforms. Practical workflows.

MetaPharm Clinical Research Inc. combines validated clinical systems with pragmatic workflows so sponsors gain speed without sacrificing quality or compliance.

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Medidata Rave

Industry-standard EDC for database build, UAT, query management, and clean data delivery.

eCOA / ePRO

Technology-driven patient data collection via tablets, smartphone apps, and electronic diaries to reduce burden and improve compliance.

SAS® Analytics

Validated statistical programming for reproducible analyses, CDISC deliverables, and CSR-ready outputs.

Safety Workflows

Structured SAE processing, reconciliation, and reporting pathways aligned to regulatory timelines.

Partnerships

Trusted by sponsors who value quality and collaboration

“MetaPharm Clinical Research Inc.’s collaborative approach and attention to quality made our program feel supported at every milestone.”
Clinical Development Lead
Biotech Sponsor

“Their therapeutic expertise and site relationships helped us stay focused on enrollment without compromising data integrity.”
Head of Clinical Operations
Pharmaceutical Sponsor

“From strategy through biostatistics, the team operated as a true extension of our organization.”
VP, Regulatory Affairs
Medical Device Sponsor

Next step

Ready to discuss your clinical development plan?

Contact MetaPharm Clinical Research Inc. to explore strategic consulting, study execution, and full-service CRO partnership across Canada and global programs.