Intensive Drug Monitoring Solutions


System-Based Informatized Solutions to Effectively Improve Efficiency and Save Cost

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During the Project Planning Phase, Our Professional Pharmacovigilance Team Assists in Program Development

  • Formulation: Develop specific monitoring plans based on product characteristics and existing safety information

  • Communication with Regulatory Authorities: Communicate closely with regulatory authorities in the early stages of the project to ensure that the plan meets regulatory requirements


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During the Project Implementation Phase, We Adopt Professional Systems for Drug Monitoring.

  • Establishment of an Electronic Information Processing Platform: system is developed to reduce human labor to improve efficiency and reduce costs

  • Electronic Data Management: electronic management, information collection, data entry, processing, auditing and assessment, to ensure completeness and accuracy

  • PV Medical Writing: writing project plans and summary reports for standardization, normalization, efficient communication and implementation

  • One-Time Entry: to solve problem of information collection requirements of efficacy and security database

  • Automatic Forwarding/Generation of Specified Format Tables: Efficient and accurate reporting of security information

  • Compliant with Regulatory Requirements: In post-marketing studies, non-serious adverse reactions also need to be reported to the ADR Center within 30 days