PharmaOps: One Platform for Regulatory, Safety, Quality, Field Force, and Tenders
A seven-module platform for pharma manufacturers that drafts dossiers, processes safety cases, runs quality investigations, supports field teams, and assembles tender bids.
The Challenge
Pharma manufacturers run registrations, safety reporting, quality investigations, field reporting, and tenders across separate spreadsheets and inboxes. Every one of them has hard deadlines and inspectors who expect a clean paper trail, and every one of them is short on people.
Key Capabilities
Dossier Factory
Registration dossiers drafted from one approved source of product data, with a gap heat map per product and market and a readiness gate before submission.
Pharmacovigilance Copilot
Safety cases taken in from email, web forms, and WhatsApp, facts extracted with the source quoted, seriousness decided by rules, and reporting deadlines counted down automatically.
QA Command Center
Deviations, root cause drafts, CAPAs with escalation, and repeat-issue detection, with inspection packs assembled as you go.
Field Force Intelligence
Rep notes turned into structured call reports, doctors ranked by a transparent score, and a next-best-action queue for every rep.
Tender Desk
Tender documents parsed, eligibility checked against your licenses and certificates, pricing calculated, and bid packs assembled with deadline tracking.
Copilot and Autonomy
Ask anything across every module in chat, while scheduled agents prepare a morning briefing and queue their work for review.
The Results
All seven modules are built and demo-ready, with the copilot answering live questions across the platform. Available as a custom build for manufacturers, distributors, and regulatory teams.
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