Certified Startup
CONVOLVE TECHNOLOGIES
Sector:
IT/ITeS
Business Model:
B2B B2B B2B
Industry:
Enterprise Applications
Technology:
Web technologies Web technologies Mobile Apps Web technologies Mobile Apps
About
Incorporation Date
Jul 28, 2020
Incorporation Type
Registered Partnership
Registered State
Kerala
Registered District
Ernakulam
Registered Address
81, Mulleppilly Road, East Kadungalloor, Aluva, 683102, Ernakulam Dist, Kerala, India
Office State
Kerala
Office District
Ernakulam
Office Address
66/1069 A, 2nd Floor, Velleparambil, Veekshanam Road, Kochi : 682018
Team
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Manoj C M
Co-founder
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Bibin Bhanujan
Co-founder
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Necer Ashraf
Founder
KOMPOUNDER (Real-Time Track & Trace for Antibiotic & Narcotic Drug Dispensing)
Empowers licensed pharmacists to log daily antibiotic and narcotic stock, sales, patient, and prescriber details with GPS-tagged operations and PDF billing. Reusing i-AUSHADHI's proven RBAC and notification backbone, it provides real-time oversight and automated non-compliance escalation to regulators to prevent unauthorized drug sales.
Sector:
IT/ITeS
Industry:
Enterprise Applications
Business Models:
B2B
Technology:
Web technologies

1. OBJECTIVE & OVERVIEW
KOMPOUNDER is a pharmacy-facing web application designed for the Drugs Control Department, Government of Kerala, to prevent the unauthorized sale and misuse of antibiotics and narcotic drugs. It ensures that only licensed, verified pharmacists dispense these critical medications while giving regulators transparent, real-time visibility into inventory and sales.

2. THE i-AUSHADHI ADVANTAGE (WHY BUILD ON EXISTING INFRASTRUCTURE)
Unlike a blank-slate proposal, KOMPOUNDER is built as a dedicated module on top of i-AUSHADHI—Kerala's existing Drug Control Repository & Compliance Management System.
• Core Analytics Ready: Our live Sales Data Analysis engine already runs automated rules for narcotic-sale detection, missing-prescription flags, and volume-spike alerts.
• Proven Infrastructure: Reuses i-AUSHADHI’s 10-role access hierarchy (RBAC), multi-channel alert distribution engine, and Stock Holder registration system.

3. KEY FUNCTIONAL FEATURES
• Pharmacist Verification & Authentication: Captures pharmacy location, pharmacist credentials, and enforces Aadhaar-linked OTP authentication for every login session.
• Daily Stock & Sales Capture: Structured daily ledger capturing drug name, dispensed quantity, patient details, prescribing doctor, and running stock balance with mandatory daily reconciliation prompts.
• Automated Compliance Engine & Alerting: Evaluates sales against configurable usage thresholds (e.g., 100-unit limits) and triggers automatic district-level alerts to assigned drug inspectors when updates lapse or thresholds are breached.
• Field Verification Tools: GPS tagging of pharmacy operations and PDF billing upload attached to every transaction for cross-verification.
• Usage Matrices & Dashboards: Auto-generated daily and monthly usage matrices for pharmacists, alongside district- and state-level compliance dashboards for regulatory enforcement.

4. TECHNOLOGY STACK & SECURITY
• Architecture: Responsive Web / Mobile-ready Client → Node.js/Express REST API (JWT-authenticated) → MongoDB Atlas.
• Security & DPDP Act Compliance: Server-enforced geographic scoping, immutable audit trails on all state-changing actions, encrypted transport (HTTPS) and at-rest database encryption.

Real-Time Inspection Reporting System
Eliminates inspection paperwork by equipping drug inspectors with on-device checklists, offline-tolerant NSQ/banned-drug advisories, and NPPA price-control notices. Features automated PDF generation, Controlling Officer review workflows (showcause/prosecution remarks), eOffice/CRU routing, and an executive dashboard tracking statewide compliance and inspection trends.
Sector:
IT/ITeS
Industry:
Enterprise Applications
Business Models:
B2B
Technology:
Web technologies Mobile Apps

1. OBJECTIVE & OVERVIEW
The Real-Time Inspection Reporting System transitions the Drugs Control Department from delayed, hard-copy inspection reporting to instant, zero-paper digital submissions from the field. It equips officers with on-device regulatory intelligence during site visits while giving senior management real-time dashboards of statewide compliance rates and inspection trends.

2. THE i-AUSHADHI ADVANTAGE (ALREADY BUILT & RUNNING TODAY)
Of all three requirements, this module has the strongest immediate readiness. The core Field Inspection workflow is already live in production within the i-AUSHADHI platform today:
• Live Capabilities: Officer-side scheduling, versioned checklist templates, on-site draft capture with photo evidence, Controlling Officer review (Approve/Escalate/Reopen), automatic PDF report generation, and status-based analytics dashboards are already running.
• Bounded Scope: Delivery focuses purely on adding three specific extensions: an in-inspection advisory feed panel, NPPA price-control notices, and eOffice/CRU routing.

3. KEY FUNCTIONAL FEATURES
• Real-Time Field Submission: Tablet-optimised web app allowing inspectors to complete versioned compliance checklists (Compliant / Non-Compliant / NA), attach geo-tagged photo evidence, and submit instantly on-site.
• On-Device Regulatory Intelligence: Built-in reference panels displaying live Not-of-Standard-Quality (NSQ) alerts, banned-drug advisories, and NPPA price-control notices directly alongside the inspection checklist—with offline caching for field connectivity gaps.
• Controlling Officer Review & Legal Action: Immediate automated notification to the Controlling Officer upon report submission. Includes structured review actions to verify findings and embed formal legal remarks ("Issue Showcause" / "Initiate Prosecution").
• eOffice / CRU Integration: Dedicated routing connector that automatically pushes verified inspection reports and Controlling Officer remarks into the Department's Central Receipt Unit (CRU) in eOffice for seamless clerical procedure.
• Executive Analytics Dashboard: Real-time visual reporting for senior leadership, tracking inspection frequency, officer workload, district-level compliance rates, and enforcement trends.

4. TECHNOLOGY STACK & SECURITY
• Architecture: Tablet-Optimized Responsive Web App → Node.js/Express REST API → MongoDB Atlas.
• Security & Compliance: Server-enforced role-based access control (RBAC) and geographic scoping, complete immutable audit logging, and encrypted data transfer.

MEDWATCH - Public Drug Quality Verification, Powered by Live Regulatory Data
Provides a simple, intuitive interface for citizens to check whether a drug batch is standard-quality, Not-of-Standard-Quality (NSQ), or spurious. Sourced directly from official lab reports and national testing pipelines, it features OTP registration, push notifications for safety alerts, and strict public-to-regulatory data isolation.
Sector:
IT/ITeS
Industry:
Enterprise Applications
Business Models:
B2B
Technology:
Web technologies Mobile Apps

1. OBJECTIVE & OVERVIEW
MEDWATCH empowers ordinary citizens to check the quality status of any medicine batch before consumption. By connecting public queries directly to official testing laboratory outcomes, it improves public awareness, supports informed purchasing decisions, and fosters transparency in Kerala's pharmaceutical retail sector.

2. THE i-AUSHADHI ADVANTAGE (WHY BUILD ON EXISTING INFRASTRUCTURE)
MEDWATCH is designed as a secure, read-only public layer over i-AUSHADHI—the Drugs Control Department's internal repository of Not-of-Standard-Quality (NSQ), Spurious, and Standard-Quality drugs.
• No External Data Dependency: The Department's own draft-to-verify-to-publish Lab Report pipeline already runs in our system. Every drug record is already stamped with a stable identity key (normalised drug name + batch number) and a public-status field.
• Complete Data Isolation: A rate-limited public API surfaces only the verified quality status, ensuring public traffic never touches or impacts internal regulatory workflows.

3. KEY FUNCTIONAL FEATURES
• Batch & Drug Name Verification: Simple, intuitive search interface where users input a batch number and medicine name to receive clear plain-language status results ("No adverse finding", "Not of Standard Quality — do not use", or "Spurious — report immediately").
• Citizen Registration & Security: Mobile app and responsive web access with simple OTP-based registration linked to mobile number, name, and email.
• Real-Time Safety Alerts: Push notifications alerting users immediately if an adverse NSQ or spurious finding is published for a batch they previously searched or within their region.
• Integrated Regulatory Content: Seamless integration with the Department's official website content for public safety advisories and regulatory notices.
• Multi-Lab Data Ingestion: Extensible pipeline designed to incorporate testing results from accredited state and national drug-testing laboratories across India.

4. TECHNOLOGY STACK & SECURITY
• Architecture: Public Mobile App / Responsive Web → Isolated Read-Only REST API (Node.js/Express) → MongoDB Atlas.
• Security & Privacy: Strict rate-limiting and abuse protection on public endpoints, minimal personal data collection aligned with the DPDP Act 2023, and complete database decoupling from internal regulatory records.

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