
Clinical Trial Services:
Clinical Development:
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Develop clinical trial protocols and/or investigational plans
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ICF Development with local language translations,
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SOPs and WI development
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Case Report Forms for Paper And EDC studies
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Investigator Brochures
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Essential Documents
Investigator /Site Management:
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Liaison between investigational sites, and CROs
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Project Management Activities
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Ethics Committee Management
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Monitor Activities
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Site Coordination for data collection and query management
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Case Study Report (Clinical Study Report) Services:
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Conduct basic statistical analyses for technical support of molecule.
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Generate clinical study reports.
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Conduct literature reviews.
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Evaluate and report on adverse events associated with the molecule.
Clinical Trial Project Management:
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Manage site feasibility, recruitment/selection
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Conduct investigator meeting
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Management of clinical study site.
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Ethics Committee Submissions
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Oversee project budgets, budget change forms, accruals, and monthly reports
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For more information email us at info@pharexcelconsulting.com or contact us today.

