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Literature Management Software

Clinevo Pharmacovigilance / Drug Safety Literature Management software is an AI enabled software designed to assist pharmaceutical companies, CROs, regulatory agencies, and healthcare organizations in managing the vast amount of scientific literature relevant to drug safety and surveillance.


Clinevo Pharmacovigilance / Drug Safety Literature Management software offers features and functionalities tailored to the unique requirements of pharmacovigilance, including:

Image Automated Literature Search

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software can automatically search and retrieve relevant scientific literature from various sources, such as PUBMED, EMBASE, medical journals, regulatory databases, clinical trial repositories, and adverse event reporting systems.

Image Literature Screening and Prioritization:

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software streamline the screening process by allowing users to categorize, tag, and prioritize literature based on predefined criteria such as relevance to specific drugs, adverse events, or regulatory concerns.

Image Integration with PV Databases:

  • Finalized literature articles can be pushed to any PV databases (ex. Argus, ArisG, Clinevo Safety, etc) in Clinevo Pharmacovigilance / Drug Safety Literature Management software.

Image Compliance Tracking

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software helps ensure compliance with regulatory requirements by tracking literature review activities, documenting decision-making processes, and maintaining audit trails of pharmacovigilance activities.

Image Reporting and Analytics

  • Clinevo Pharmacovigilance / Drug Safety Literature Management Software Advanced reporting and analytics capabilities enable users to generate custom reports, visualize trends, and identify potential safety signals or emerging risks based on literature analysis.

By leveraging our Clinevo Pharmacovigilance / Drug Safety Literature Management software, you can:

Improve efficiency and productivity in pharmacovigilance literature management processes.

Enhance the quality and reliability of safety data and signal detection.

Ensure compliance with regulatory requirements and industry best practices.

Gain valuable insights to support risk management and decision-making in drug safe

Image Easy to Use Interface

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software is a cloud-based software solution to manage vast volumes of scientific literature, patents, and research findings electronically which is also easily accessible. Clinevo Literature Intake comprises user friendly interface so as to facilitate easy and comfortable work experience with the software which can be integrated with any PV Database such as Argus, ArisG, Clinevo Safety, etc.

Image Real time monitoring, Dashboards and reporting

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software provides powerful and actionable dashboards and reports for real time monitoring and tracking of quality and compliance.

Image Anytime, Anywhere & Any device

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software is a user-friendly web application which can be accessed with internet / intranet using IE, Chrome and Firefox browsers and on any device that enables real-time site collaboration and document exchange.

Image Regulatory Inspection Ready

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software complies with all current and emerging regulations including 21 CFR Part 11, ANNEX 11, GxP, and GDPR.

Image WORKFLOWS AND VERSION CONTROL

  • Clinevo Pharmacovigilance / Drug Safety Literature Management software provides Robust Workflows for Review, Medical Review, Quality Checks and Approval, etc.

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