Technology
Technology
MetaPharm Inc. combines validated clinical systems with pragmatic workflows so sponsors gain speed without sacrificing quality or compliance.
MetaPharm Inc. combines validated clinical systems with pragmatic workflows so sponsors gain speed without sacrificing quality or compliance.
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.
Clinical workflow
From design through submission — a connected path that keeps quality and compliance visible at every step.
01
Design
Protocol, CRF, and database specifications aligned to endpoints.
02
Build
EDC configuration, edit checks, and UAT with sponsor sign-off.
03
Conduct
Monitoring, query resolution, and continuous data quality review.
04
Analyze
Biostatistics, SAS® programming, and validated output packages.
05
Submit
CSR support and regulatory-ready documentation.
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.