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Allphase Clinical Research offers a full spectrum of data management services
and expertise to ensure the efficient and appropriate management of your clinical
trial data. Our team is experienced in clinical trial design, implementation and
execution at all levels. They are well trained and rigorously follow Standard
Operating Procedures (SOPs) that encompass security, industry regulations,
engineering and GCP. Using state-of-the-art data management system technology,
we are able to deliver a high-quality, unified database.
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Our services include:
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CRF and database design
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AE and medical coding and reporting
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Internet-based randomization system
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Clinical trial safety database/ reconciliation
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Lab data import
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Single and double data entry
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Electronic Data Capture
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Query generation
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Data validation, storage and archiving
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Biostatistics
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