Build Rule 39AA-ready QR coding directly into your existing pharmaceutical packing lines with secure code generation, ERP data integration, inline printing, machine vision verification and consumer authentication.
Product, manufacturer, batch and expiry information.
High-speed printing with machine vision verification.
Mobile product verification without app installation.
Live batch and expiry data from enterprise systems.
Four connected capabilities make Rule 39AA coding work reliably in production: master data, controlled code generation, print verification and consumer response.
Select coding, vision, code management and enterprise integration technologies based on substrate, production speed and pharmaceutical packaging requirements.
Representative solution scenarios for pharmaceutical companies implementing QR coding across Indian packaging and distribution operations.
The measures a QA head, a packaging development head and a regulatory affairs lead want evidence for. Targets are design goals agreed in writing.
Coding is introduced line by line so production output remains protected while compliance and verification capabilities are implemented.
Review notified products, artwork files, available print areas and the location of prescribed data fields within your enterprise systems.
Conduct substrate trials, select the appropriate coder and camera, define code size and position and document integrations.
Run live coding against agreed quality, read-rate and throughput criteria using your actual cartons, foil and labels.
Commission remaining lines, prepare qualification documentation and move the system into ongoing support and maintenance.
Engineer Rule 39AA coding directly into your packaging operation rather than adding an isolated print module.
We map prescribed data requirements into the actual coding and verification workflow.
Test foil, board and label materials with candidate printers before hardware procurement.
Coding hardware, vision, code vaulting and consumer response can be integrated by one engineering team.
Audit trails, electronic signatures, access control and retention requirements can be included in the system design.
It is a machine-readable barcode or QR code required under Rule 39AA of the Drugs Rules for notified medicines. The prescribed information can include the unique product identification code, generic and brand name, manufacturer details, batch number and expiry dates.
Yes. The solution is designed around your existing packing lines, artwork constraints, print area, line speed and enterprise systems. The implementation starts with a requirement study before coder, camera and integration requirements are finalized.
The appropriate coding location depends on the product format, available print area, artwork and applicable requirements. Primary and secondary packaging options can be assessed SKU by SKU during the artwork and line assessment.
Yes. The solution can integrate with systems such as SAP, Oracle, Microsoft Dynamics, Navision and Tally so that batch, manufacturing and expiry information can be sourced directly rather than manually entered at the production line.
Thermal inkjet and laser coders, industrial vision cameras, lighting systems, sensors and automatic rejection mechanisms can be integrated based on the substrate, print area, required code quality and production line speed.
Yes. Code generation, vaulting and line-control functions can be deployed on-premise. A hybrid architecture can also be used where the consumer-facing scan response is hosted through a public endpoint.
A single-line pilot can typically be planned within approximately eight to twelve weeks after requirements are finalized, depending on hardware lead times, artwork revisions, integration complexity and the customer validation process.
Packaging artwork may need revision to reserve the required code area, quiet zone, contrast and fixed print position. These requirements are assessed during the artwork and packaging-line study.
Yes. A controlled code repository can maintain code lifecycle status, allocation and retirement records, helping prevent duplicate identifiers and enabling traceability of codes across batches.
Post-go-live support can include preventive maintenance, software updates, coder and camera support, consumables planning, incident response, regulatory data-format changes and an agreed annual maintenance arrangement.