In addition to its pharmacovigilance services, PVigi also offers a range of contract research organisation (CRO) services to support the clinical development of pharmaceutical products. These services include:
Clinical Trial Management: PVigi provides comprehensive clinical trial management services, including protocol development, site selection, patient recruitment, and data management.
Medical Writing: PVigi offers high-quality medical writing services, including the development of clinical study protocols, investigator brochures, and regulatory documents.
Regulatory Affairs: PVigi assists clients in navigating the complex regulatory landscape, ensuring compliance with local and international regulations.
Quality Assurance: PVigi conducts quality assurance audits to ensure that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines. We have compliance with local and international regulations.
Safety Submissions: PVigi provides SUSAR, DSUR, Annual report submissions to Ethic Committee and Ministry of Health.
CRO Activities
Contract Research Organisation
In addition to its pharmacovigilance services, PVigi also offers a range of contract research organisation (CRO) services to support the clinical development of pharmaceutical products. These services include:
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