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A trusted and globally compliance safety database
Solutions for Drugs, Devices, Vaccines,
Combination Products, Veterinary and Human in pharmacovigilance. Enhance safety with advanced automation and compliance at every step.
What makes Pharmacovigilance software by Sarjen stand out?
We understand there are unique challenges you may face during the PV process. PvEdge Automation tackles these challenges by ensuring tasks are completed promptly, allowing your team to focus on other critical priorities and drive innovation in pharmacovigilance.
Intake/ Triage
MICC
Literature
Regulatory
Web Intake

Multi Source Inbox
Case

Workflow
Case Processing
MedDRA Auto Update
Patient Narrative
QC Checklist
XML Validator
Labelling & Casualty Matrix

R2 XML
R3XML
CIOMS
Medwatch
VAERS
MDAERF
AS2

Gateway
Submissions
FDA
MHRA
EMA
PMDA
TGA
KFDA

Quality process, Doc management, Training management

Safety data exchange agreement

Report Automation PSUR /PADER/ TDC publishing

Risk management plans

Proporational reporting ration (PRR) and Chi square algorithm
Impact
0
k+
Case processed yearly
0
k+
Legacy data migrated
0
k+
ICSR's submitted yearly
0
+
MAH’s served
Features
Multivigilance
Multi-tenant
Cloud ready
Globally compliant
Pre validated
Rapid implementation
AI-enable
Return on investment
Automate Pharmacovigilance activity to the next level
Enhance your pharmacovigilance process with advanced automation. Streamline operations, boost accuracy, and achieve unparalleled safety with our cutting-edge solutions.
Other domains served by Sarjen
Want to know more about PvEdge