Literature Monitoring

Literature screening in pharmacovigilance is a critical process that involves searching, retrieving, and evaluating information from various sources to identify potential safety concerns with a drug or medical device. It is a systematic and ongoing process of searching, reviewing, and analyzing published literature and other sources of information for potential adverse drug reactions, new safety concerns, and other relevant pharmacovigilance information. This information is used to identify potential signals of harm and support drug safety decision-making. 

Literature monitoring is an important component of pharmacovigilance, as it helps ensure that the latest safety information is incorporated into the benefit-risk assessment of marketed drugs.

We deliver Literature Monitoring Services leveraging our TOTALVigilance framework that is a cost-effective, flexible, and scalable solution designed to reduce manual effort through digitalization, automation, and real-time oversight. It combines expert knowledge, lean processes, and modern technology to deliver high-quality, compliant services. With adaptable service models and seamless integration into your existing systems and workflows, TOTALVigilance enhances operational efficiency, enables proactive oversight, and maximizes return on investment.

With over 15+ years experience, Our highly specialized PV team can help marketing authorization holders to conduct medical literature surveillance at least weekly according to the GVP module VI and based on the required frequency as described by the local regulatory authorities, both for globally indexed literature databases and locally (non-indexed) literature journals.

Digital & Automated Literature Monitoring Services with Realtime & Pro-active Oversight

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Leverage our 15+ years of comprehensive experience and our portfolio of System Integration (SI) and Managed Cloud Services to enhance regulatory compliance in pharmacovigilance.

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Manual oversight is often inefficient and error-prone, leading to compliance risks. As a result, there is a growing need for a digital, automated PV oversight framework to enhance efficiency, data quality, and real-time regulatory compliance

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Unique SaaS platform that co-exist with drug safety databases enable companies to proactively manage and automate global Pharmacovigilance compliance operations.

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Life sciences organizations need a modern delivery framework that is purpose-built for agility, scalability, and compliance to efficiently address all of the regulatory obligations towards Pharmacovigilance.

TOTALVigilance - Functional Services

Simplify End-to-End Pharmacovigilance Compliance Obligations by combining People, Process, Technology, Automation & Quality.

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