Pharmacovigilance Writing Services
Pharmacovigilance Writing Services in India.
Audit-ready pharmacovigilance writing, PSUR/PBRER, DSUR and literature monitoring, supported by our FAERS-driven PV Resource Allocation Tool and ICH E2C(R2) / GVP Module VI compliant processes.
What we deliver
Pharmacovigilance Writing Services for PV departments and CROs.
PSUR / PBRER writing
DSUR and aggregate safety reports
ICH E2C(R2) compliant periodic literature reviews
FAERS-based PV resource planning
Validated search strings, evidence tables and audit trails
Why Ichelon
Quality most vendors can't match.
We run every deliverable through the Publication Readiness System™, a 4-layer sequential QC (Scientific, Editorial, Compliance, Technical) governed end-to-end by SOPs. Journal fit is engineered before a single word is written, using our AI-verified Scientific Writing Tool. The result: submission-ready manuscripts with embedded global reporting standards and a complete audit trail.
Explore the Scientific Writing & MedComm practiceFrequently Asked Questions
Questions, answered.
Yes. Our literature monitoring is built to ICH E2C(R2) and GVP Module VI, with validated search strings, evidence tables and complete audit trails, defensible at inspection.
Our proprietary PV Resource Allocation Tool uses FAERS-driven drug-risk tiering to produce defensible, audit-traceable staffing plans.