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BioPharma Services Inc.

About

BioPharma Services Inc. is a full-service Contract Research Organization (CRO) specializing in Phase I/IIa, Bioequivalence, Human Abuse Liability, PET Imaging, and Psychedelic Studies. With over 17 years of industry experience and a state-of-the-art research facility in Toronto, Canada, we are committed to delivering high-quality clinical research with speed, efficiency, and compliance. AI-Driven Patient Recruitment & Expanded Capabilities: Through our connection with WELL Health Technologies, BioPharma now leverages AI-powered analytics to accelerate and optimize patient recruitment. By analyzing real-world clinical data, we can rapidly identify eligible participants, improving enrollment timelines while maintaining strict ethical and regulatory standards. Our in-house GLP/GCP bioanalytical services, featuring LC-MS/MS technology, provide high-precision analysis to support both preclinical and clinical research. BioPharma remains fully compliant with FDA, Health Canada, and ANVISA regulations and has successfully passed all major regulatory inspections. Key Highlights ✔ 150+ bed capacity in a cutting-edge Toronto-based clinical facility ✔ AI-enhanced recruitment ensures 99% enrollment for all Phase I studies with a 95% completion rate ✔ Accelerated study startup: 30-Day CTA approval, Weekly IRB/Ethics review ✔ 20,000+ active subject database, including special populations & healthy volunteers ✔ Full-service CRO: Regulatory Affairs, Scientific & Medical Expertise, Project Management, Biostatistical Analysis (CDISC-compliant SDTM & ADaM datasets), Medical Writing, and more At BioPharma Services, we combine industry expertise, AI-driven recruitment, and operational excellence to deliver timely, reliable, and high-quality clinical research for our global clients.

Country

CA

Address

4000 Weston Road, Toronto, ON

Postal Code

M9L 3A2

Company Type

Privately Held

Employees

296

Industry

Research Services

Specialties

Bioequivalence (BE) Studies; Phase I/IIa clinical trials; Pharmacokinetic Analysis; Regulatory Affairs; Data Management; Quality Assurance; Project Management; Statistical Services; Human Abuse Liability/Potential; Biometrics/CDISC; Bioavailability; Psychedelic Research; Clinical trial monitoring; Medical and regulatory writing; pharmacovigilance; Subject recruitment and retention services; Rare disease studies; PET Studies; Full-service CRO

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