Search strategy and database list
Practical, reviewable, and ready for the owner who needs to act, approve, or respond.
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Reviewed
Search Log
StatusReviewed
Our craft
Built around real pharmacovigilance practice.
Service Detail
Monitor literature with traceable safety decisions.
PharmaRevix performs global and local literature monitoring for adverse drug reactions, safety signals, and relevant medical literature in line with FDA, EMA, and ICH expectations.
You need routine global literature screening
You have local literature requirements in selected regions
You need auditable decisions for inspection
You need literature signals connected to case processing
Deliverables
Practical outputs your team can use immediately.
Screening calendar and reviewer assignment
Practical, reviewable, and ready for the owner who needs to act, approve, or respond.
Hit triage and relevance log
Practical, reviewable, and ready for the owner who needs to act, approve, or respond.
ADR and signal escalation records
Practical, reviewable, and ready for the owner who needs to act, approve, or respond.
Quality review checklist
Practical, reviewable, and ready for the owner who needs to act, approve, or respond.
Periodic evidence archive
Practical, reviewable, and ready for the owner who needs to act, approve, or respond.
Workflow
A clear sequence from assessment to handoff.
01
Assess
Define products, active substances, and search sources
02
Plan
Run scheduled literature searches and deduplication
03
Execute
Screen, assess, and escalate safety-relevant records
04
Maintain
Archive evidence and quality-review decisions
Proof Package
Every engagement leaves an evidence trail.
The work is designed for real review: authority questions, partner due diligence, quality audits, and internal leadership updates.
ADRSignalsSenior-led
Global and local literature monitoring
Captured with owners, assumptions, decision rationale, and next actions so the work can continue smoothly.
Search strategies aligned to product and region
Captured with owners, assumptions, decision rationale, and next actions so the work can continue smoothly.
Medical review of relevant hits and safety signals
Captured with owners, assumptions, decision rationale, and next actions so the work can continue smoothly.
Auditable documentation of decisions and exclusions
Captured with owners, assumptions, decision rationale, and next actions so the work can continue smoothly.
Related Services
Connect this work with adjacent regulatory and safety needs.
Case Processing & Submission
PharmaRevix supports ICSR receipt, triage, processing, narrative authoring, medical and quality review, and timely submissions to authorities and partners.
Explore serviceSignal Management
PharmaRevix supports signal detection scheduling, validation, prioritization, evaluation, QPPV safety review, and documentation aligned with GVP Module IX.
Explore servicePV System Setup & Maintenance
PharmaRevix builds and maintains pharmacovigilance systems, including PSMF authoring, safety database setup, SDEAs, data migration, and ongoing stewardship.
Explore serviceFAQ
Common questions about Literature Screening & Management.
Short answers for teams deciding whether this is the right next step.
Ask us anythingLiterature screening monitors global and local sources for adverse drug reactions, safety signals, and relevant medical literature in line with FDA, EMA, and ICH expectations.
The right timing depends on product stage, target markets, and regulatory commitments. PharmaRevix usually starts with a focused review and then sets a workplan with owners, dates, and evidence expectations.
Yes. PharmaRevix can scope this as a standalone workstream or connect it with adjacent regulatory affairs, pharmacovigilance, QMS, and submission activities.
Free 30-minute consultation
Need literature screening & management support?
Talk with PharmaRevix about scope, timelines, and the cleanest next step for your market or safety obligation.