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To better assist you with your request, please choose a research area provided by BiTrial CRO. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.
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Clinical Trial Design
Develop study-related protocols, case report forms (CRFs) and database tools for records management.
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Clinical Research
Determine the safety and effectiveness of medications and medical devices.
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Bioequivalence Studies
Assess the expected biological equivalence of two proprietary preparations of a drug.
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Clinical Protocol Design & Development
Creation of clinical protocol document which details how a clinical trial is designed, relating to to the methodology, hypothesis, and operation of clinical trial to ensure the safety of the patients is maintained as well as maintaining the integrity of the data collected during the trial.
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Site Monitoring
Maintain oversight over participant's health during a clinical trial.
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Patient Recruitment
Recruit and retain patients for clinical trials.
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Site Selection
Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
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Observational Research
Research method for documenting clinical, economic, and or humanistic outcomes of actual medical practice absent the constraints of a more formal experimental design. See also Pragmatic Clinical Trials.
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Case Report Monitoring & Auditing
Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
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Study/Site Feasibility Study
Explore and test study practicality.
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