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Your script for healthier scientific literature & information workflows

Your script for healthier scientific literature & information workflowsYour script for healthier scientific literature & information workflowsYour script for healthier scientific literature & information workflows

PubHive Navigator is a SaaS platform for teams in drug safety & pharmacovigilance, regulatory, MedAffairs, HEOR, and R&D.

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Goodbye Workarounds. Hello Workflow.

PubHive Navigator is a one-stop scientific workflow automation platform engineered specifically for life science teams like yours whether in Drug Safety and Pharmacovigilance (PV), MedTech Clinical Evaluation Reporting (CER), Medical Writing, Medical Affairs, Health Economics and Outcomes Research (HEOR), R&D, or Information Management.


An alternative to rigid standalone tools cobbled together with manual workarounds, PubHive Navigator is fit-for-purpose platform that optimizes existing business processes and automates repetitive work.


PubHive Navigator is powered by a proprietary Omni-Loop AI (artificial intelligence) Engine and distinguishes itself with flexible configurations, tailored workstreams, and intuitive online interfaces that make scientific information and literature handling quick and easy. 

PubHive Navigator Workflow Modules

Drug Safety & Pharmacovigilance (Pulse)

Drug Safety & Pharmacovigilance (Pulse)

Drug Safety & Pharmacovigilance (Pulse)

Pulse is PubHive Navigator's safety and vigilance workflow module for PV literature surveillance and management, signal detection and management, aggregate reporting and medical writing, and more.

Discover Pulse

Systematic Literature Reviews (Quest)

Drug Safety & Pharmacovigilance (Pulse)

Drug Safety & Pharmacovigilance (Pulse)

Quest is PubHive Navigator's workflow module for systematic literature reviews, meta-analysis projects, and other projects that involve literature searching, reviewing, management, data extraction, writing, editing, and more.

Discover Quest

R&D Literature Workflows (Fetch)

Drug Safety & Pharmacovigilance (Pulse)

R&D Literature Workflows (Fetch)

Fetch is PubHive Navigator's workflow module designed to eliminate workarounds and friction for R&D and Medical Affairs teams when working with scholarly peer-reviewed journal content.

Discover Fetch

A Single Fit-for-Purpose Platform for Life Sciences

Boost productivity with role-specific workstreams

Save time with in-workflow literature & information access

Save time with in-workflow literature & information access

scientific literature workstreams

 Only PubHive Navigator provides you with focused productivity tools to reduce manual work so you can harness scientific information and the growing universe of scholarly journal content.

Save time with in-workflow literature & information access

Save time with in-workflow literature & information access

Save time with in-workflow literature & information access

document delivery

PubHive Navigator reduces the number of systems, steps and minutes it takes to access scientific literature and information by seamlessly injecting access within workstreams & by integrating 3rd party data sources.

Centralize literature & information management

Save time with in-workflow literature & information access

Improve decision-making with analytics-driven insights

single system of record for pharmaceutical information

As a single source of truth for your team's scientific literature & information, PubHive Navigator is the only 'fit for purpose' life science software platform that eliminates siloed information & tools so you can focus on mission-critical work.

Improve decision-making with analytics-driven insights

Improve decision-making with analytics-driven insights

Improve decision-making with analytics-driven insights

scientific literature workflow analytics

 With visibility across data sources, workflows and platform usage, PubHive Navigator provides on-demand insights that enable you to continuously improve processes, performance and spending. 

Reduce risk with built-in regulatory & copyright support

Improve decision-making with analytics-driven insights

Reduce risk with built-in regulatory & copyright support

regulatory compliance pharmaceutical information

 Designed with 21 CFR Part 11, GxP quality guidelines and regulations, and international copyright in mind, PubHive® offers a validated solution so you can worry less about governance, risk and compliance (GRC) and instead focus on business results.  

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