Pharmaceutical Track and Trace

Drug Traceability from Batch to Patient

One unverified drug unit in the market is a regulatory event. Acviss Origin gives you blockchain-backed track and trace from manufacturing to dispensing — with SAP integration and full CDSCO audit readiness built in.

Built for brands and manufacturers. Not for consumers.

80+ Brands Protected 2B+ Products Secured Real-Time Verification ISO 27001 Certified

Trusted by Leading Brands

Kitply Corteva Agriscience ITC Pigeon TATA

Pharma Distribution Has Three Blind Spots

Each one is a potential liability — for your patients, your regulator, and your brand.

Serialisation Without Consumer Verification

Most pharma brands have serialisation on their packaging line, but no way for patients, pharmacists, or distributors to verify unit authenticity in the field. The code exists — but no one checks it.

C&F Agent and Distributor Opacity

After the product leaves your manufacturing plant, visibility collapses. You know what left your warehouse. You do not know where it is, whether it was diverted, or how it reached the pharmacy shelf.

Fraudulent Returns via Duplicate Packaging

Counterfeit units are returned through your distributor network as genuine product. Without unit-level identity verification at the point of return, you absorb the cost of fraud you did not create.

Regulatory Documentation Gaps

CDSCO, WHO, and export buyer audits increasingly require unit-level traceability records. Batch-level records are no longer sufficient for compliance in high-value markets and for WHO prequalification.

The Scale of the Risk

1 in 10
Medical products in low- and middle-income countries are substandard or falsified — directly endangering patient safety
Source: World Health Organization (WHO)
₹3,000 Cr+
Estimated annual revenue loss to Indian pharmaceutical companies from counterfeit drugs and parallel imports
Source: ASSOCHAM / Industry Estimates
200K+
Deaths estimated annually from substandard and counterfeit antimalarials alone in Sub-Saharan Africa — the market where Indian pharma exports are highest
Source: WHO / INTERPOL

Acviss Origin vs. Legacy Track and Trace Platforms

TraceLink, PharmaSecure, and Antares Vision each solve part of the problem. Acviss covers the full stack — from the manufacturing line to the patient's hand.

Capability Acviss Origin TraceLink PharmaSecure
Unit-level blockchain traceability Blockchain + QR Network-based Basic serialisation
Consumer / patient verification (no app) WhatsApp verify Not offered SMS/USSD only
SAP + MS Dynamics 365 integration Native integration SAP certified Limited
Geofenced territory diversion alerts Real-time alerts Not offered Not offered
Holographic + physical label options Uniqolabel + Axion Software only Software only
Warranty / return fraud prevention Assist module Not offered Not offered
Online brand protection (marketplace) Truviss module Not offered Not offered
India + emerging market focus India HQ, India-first US/EU primary India + Africa

This comparison reflects publicly available information as of 2026. Capabilities may vary by deployment scope. Acviss recommends an independent evaluation before any procurement decision.

From Manufacturing to Patient

Every handoff point is a potential entry for a counterfeit. Acviss closes each one.

Manufacturing
Certify + Origin
Unit serialisation at the line. Blockchain record initiated
QA / Batch Release
Origin
QC scan records attached to batch. Audit trail begins
C&F Agent
Origin
Dispatch scan updates blockchain. Territory geofencing active
Distributor
Origin
Receipt scan confirms handoff. Diversion alerts if zone violated
Pharmacy
Uniqolabel
Visual holographic check at dispensing. No device required
Patient
Certify
WhatsApp verify. Instant authentic or suspect result in local language
Pharmaceuticals Nutraceuticals Agrochemicals FMCG Medical Devices Export Markets Consumer Goods Manufacturing Pharmaceuticals Nutraceuticals Agrochemicals FMCG Medical Devices Export Markets Consumer Goods Manufacturing

Built for Pharma Compliance Requirements

Blockchain Track and Trace

Origin gives you unit-level visibility from manufacturing to dispensing. Every handoff creates an immutable blockchain record, audit-ready for CDSCO, WHO, and export compliance documentation.

Origin
Non-Clonable Unit Serialisation

Patented 2D codes on every unit — mathematically impossible to clone. Patients verify via WhatsApp or web browser with no app download in any language. Fake scans trigger instant alerts.

Certify
Holographic Security Labels

Uniqolabel holographic labels give pharmacists and distributors a rapid visual authentication check — no device, no scan, no delay at point of dispensing in Tier 2 and Tier 3 markets.

Uniqolabel
Return and Warranty Fraud Prevention

Assist verifies product authenticity before any return is processed. Distributors cannot raise claims on counterfeit units because every claim requires a verified authentic product identity.

Assist

From Deployment to Full Compliance Coverage

1

Serialise at the Line

Non-clonable unique codes are applied to every unit on your packaging line. Acviss works with your packaging team to ensure zero line speed impact and compatibility with your current label substrate.

2

Track Through the Chain

Origin integrates with SAP or MS Dynamics 365. Every dispatch, handoff, and receipt creates a tamper-proof blockchain record. Your supply chain team gets a real-time dashboard with full batch and unit visibility.

3

Verify at the Point of Care

Pharmacists use Uniqolabel for instant visual checks. Patients scan via WhatsApp — no app, no account. Your compliance team exports audit records on demand for any regulatory review.

What Brands Say About Supply Chain Coverage

★★★★★

"We have seen this track and trace system implemented across companies and have experience partnering with a few, but none have been as successful as Acviss."

FMC Company Representative FMC — Global Agrochemical and Life Sciences Company
★★★★★

"Acviss is helping improve our business operations and future readiness. Their quick response to technical problems and service support stands out."

Lamina Suspension Chandrashekar Shetty Lamina Suspension Products Ltd
★★★★★

"The quality of the services rendered has exceeded our expectations, and we truly appreciate the efforts of the Acviss Technologies team in delivering results that align with our goals and requirements."

Biocon Electric Rajendra Verma Biocon Electric
ISO 27001 Certified
2 Granted Patents
GS1 Certified
Global Solution
Audit-Ready Records

Get a Free Track and Trace Consultation

Talk to an Acviss pharma supply chain specialist. Bring your specific compliance requirements — CDSCO, WHO, or export buyer standards — and we will show you exactly how Origin handles them.

What Pharma Compliance Teams Ask First

Does Origin meet CDSCO serialisation requirements?
Acviss Origin supports unit-level serialisation with blockchain-backed audit records that can be formatted for regulatory submissions. We work with your regulatory affairs team to ensure output aligns with the specific documentation requirements of your target market.
How does SAP integration work?
Origin integrates natively with SAP and Microsoft Dynamics 365. The integration does not require changes to your existing ERP configuration — it adds a track-and-trace data layer that syncs with your existing SAP modules. Acviss provides technical documentation and sandbox testing before any live deployment.
Will serialisation affect our packaging line speed?
Acviss works with your packaging engineering team to ensure line speed is maintained. Multiple label application methods are available depending on your substrate and line configuration. For lines where physical labels are not viable, Phantom Code embeds authentication directly into the packaging artwork at pre-press — zero line impact.
Can it support WHO prequalification requirements for export?
Origin generates blockchain-backed provenance records that document every step in your supply chain from manufacturing to end market. These records are structured for export compliance documentation. We recommend involving your regulatory team in the specification review before deployment for export-specific requirements.
What is the typical implementation timeline?
Typical pharma deployments run 8 to 16 weeks from contract to live production — covering packaging line integration, ERP connection, distributor onboarding, and system validation. A phased rollout starting with primary SKUs and key distributors is recommended for large portfolios.

Your Next Regulatory Audit Needs Unit-Level Records

Book a live demo of Acviss Origin. See how blockchain track and trace handles your specific supply chain — from manufacturing line to patient verification.

Schedule My Demo →