Delivering Safety across the product life cycle with comprehensive Literature Monitoring Services

At Navitas Life Sciences, we understand the critical role that literature monitoring plays in ensuring the safety and efficacy of your products. Our team of experienced PV subject matter experts is here to support your clinical pharmacovigilance needs with cutting-edge AI-driven global and local literature monitoring solutions. Our Literature Monitoring as a Service (LMaaS) can be tailored to your organization’s specific requirements, offering flexible single-service options to meet your needs.

Customizable and Cost Effective Solutions

Are you looking to outsource your literature monitoring? Our literature monitoring processes are designed to comply with all global and local safety requirements. We provide customizable, flexible, and cost-effective service solutions, supported by best-in-class technologies.

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Our comprehensive Literature Monitoring Services include

Defining Literature Search Strategy

Defining Literature Search Strategy

Crafting tailored search strategies to ensure comprehensive coverage
Global Literature Screening

Global Literature Screening

Utilizing databases such as Embase, PubMed, and customer-specified databases for thorough screening
Medical Literature Monitoring

Medical Literature Monitoring

Ongoing surveillance to identify relevant safety information
Local Literature Screening

Local Literature Screening

Adhering to local regulatory requirements for literature monitoring
Procurement and Review of Full-Text Articles

Procurement and Review of Full-Text Articles

Ensuring access to and thorough review of necessary articles
Translation Services

Translation Services

Certified translators provide accurate translations of literature articles

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Automation of literature search and review

Over the years, pharmacovigilance (PV) processes have relied on PV professionals manually sifting through large volumes of data to identify, assess, and report Adverse Event (AE) information.

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Gen AI in PV and Regulatory Affairs

Exploring targeted applications of Gen AI within PV and Regulatory Affairs, highlighting its potential to streamline processes, improve decision-making, and ultimately, drive better outcomes for stakeholders.

Gain the Navitas Life Sciences Edge

Experienced Team

Experienced Team

Providing expert support throughout your PV processes
Domain Experts

Domain Experts

30+ years as a trusted partner offering strategic advice and improving your PV operations
Bespoke Services

Bespoke Services

Tailoring solutions to your unique needs
Industry-Leading Networks

Industry-Leading Networks

20+ years of unparalleled PV insight and benchmarking
Commitment to Quality and Compliance

Commitment to Quality and Compliance

Maintaining high standards and error-free operations
Global Infrastructure

Global Infrastructure

Delivering flexible and proximity-based solutions

BLOGS

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Strategizing Artificial Intelligence in Regulatory Affairs and Pharmacovigilance

Ensuring patient safety and compliance with global PV regulations is paramount; our robust Regulatory and PV services integrate AI to enhance efficiency and accuracy.
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Showcasing as a knowledge-based full services CRO: Insights on PV and Precision Medicine

At Navitas Life Sciences, we believe in not just advancing the frontiers of pharmaceutical sciences, but also in giving back to society and academia. Read our blog to learn more.
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Combating counterfeit medicines: Insights from Global QPPV

In the fight against counterfeit medicines, the stakes are incredibly high. Counterfeit drugs pose significant threats to public health worldwide, with far-reaching consequences, especially in regions with limited regulatory oversight. At Navitas Life Sciences, we are dedicated to addressing these challenges head-on.

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