BPCL QC Platform – Unified Digital Ecosystem for Lab Operations
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BPCL Unified Quality Control Digital Platform

Digitizing Laboratory Operations, Proficiency Testing & Reference Material Management

Executive Vision

"Build a unified digital ecosystem that integrates Laboratory Information Management (ILIMS), Proficiency Testing (PT), Reference Material Producer (RMP), Laboratory Quality Management (LQMS), and Executive Dashboards into a single Quality Intelligence Platform."

Move from fragmented applications to a connected quality ecosystem enabling real-time operational intelligence and enterprise-wide visibility.

Strategic Objective: Replace isolated legacy LIMS software, uncontrolled desktop spreadsheets, physical paper registers, and email-based circulars with one immutable, sovereign system of record.
Core Value Realization Pillars
  • One Unified Platform: Connecting Laboratory Operations, Proficiency Testing, and Reference Material Management under a single pane of glass.
  • Real-Time Quality Intelligence: Instant leadership visibility across national zones, regional administrative clusters, and refinery laboratories without manual deck assembly.
  • Standardized & Accelerated Processes: Reduced manual effort, elimination of transcription errors, and faster sample turnaround times (TAT).
  • Commercial & Compliance Expansion: Improved customer experience, self-service adoption, expanded revenue from commercial testing and CRMs, and continuous accreditation readiness.
Shared Cloud Core: Deployed in Microsoft Azure India (100% sovereign data residency) with unified SSO, MFA, maker-checker authorization, and immutable WORM audit logs.
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Unified Platform Architecture - Overview

Core Business Modules Funneling into a Single Unified Application

4 Core Business Modules (Source Engines)
PT
Proficiency Testing (PT)
Digitizes the complete proficiency testing lifecycle, including scheme management, participant onboarding, evaluation, publication, and certification. Includes an enterprise dashboard and analytics.
RMP
Resource Material Provider (RMP)
Manages the complete lifecycle of certified reference materials, from production planning to certification, distribution, inventory management, and commercialization. Includes an enterprise dashboard and analytics.
LIMS
Integrated Laboratory Information Management (ILIMS)
Digitizes complete laboratory operations from sample receipt through testing, validation, reporting, retention, and disposal. Includes an enterprise dashboard and analytics.
LQMS
Laboratory Quality Management System (LQMS)
Combines Document Management (DMS), Quality Management (QMS), audit, calibration, stock, learning, and Smart Lab monitoring in one governed QA portal. Includes an enterprise dashboard and analytics.
Unified Quality Control Digital Application

All four engines converge into one unified digital portal architecture with shared data structures and automated cross-module interlocks:

  • Active Safety Interlocks: If an instrument's calibration expires in LQMS, ILIMS automatically locks that instrument from sample testing.
  • Single Source of Truth: Every record is entered once at the source and shared across modules without manual re-keying.
  • Zero Data Divergence: Certificates of Analysis (CoAs) are generated directly from study and raw instrument records.
  • Direct Outbound Instrument Push: Outbound-only IoT collector gateways eliminate manual transcription from lab instruments.
Reviewer Structure Funnel: [PT + RMP + ILIMS + LQMS] ➔ Unified QC Digital Application ➔ Single Command & Control.
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Proficiency Testing (PT) Digital Platform

Provide a standardized, scalable, and compliant platform for managing proficiency testing programs.

End-to-End Operational Flow (9 Steps)
1
PT Scheme Design & Approval
Configure annual scheme parameters, test matrices (fuel, lubricants), and technical approvals.
2
Scheme Publication
Publish annual PT calendars, round dates, and round parameters to the public portal.
3
Participant Registration & Enrollment
External industry laboratories register online, select rounds, and configure points of contact.
4
Payment Confirmation
Payment gateway integration with automated GST invoicing and enrollment confirmation.
5
Sample Preparation, Dispatch & Receipt
Homogenized sample packaging, courier API tracking, and digital receipt confirmation.
6
Results Submission
Participant labs enter results directly into secure, time-locked online forms before deadlines.
7
Evaluation & Review (ISO 13528)
Automated calculation of robust statistics (z-scores, zeta-scores, En numbers) with zero calculation errors.
8
Publish PT Report
Automated generation of anonymized round summary reports and performance distribution histograms.
9
Certification & Archival
Instant issuance of accredited participation certificates and permanent WORM archival.
Key Capabilities
  • Scheme Management: Multi-round annual calendars, round matrices, parameter limits.
  • Participant Onboarding: Self-service portal for internal and external laboratories.
  • Payment Tracking: Automated reconciliation, payment gateway integration, GST invoices.
  • Logistics & Dispatch: Courier API integration with end-to-end shipment status.
  • Certificate Generation: Cryptographically signed, verifiable digital certificates.
  • Audit Evidence Management: Complete forensic logs of submissions and reviews.
Business Benefits
  • Increased Participation: Attracts external commercial and PSU laboratories across India.
  • Faster Evaluation Cycle: Cuts statistical report turnaround from weeks to hours.
  • Improved Customer Experience: Seamless digital enrollment and instant certificate downloads.
  • Accreditation Readiness: 100% compliant with ISO/IEC 17043 & NABL regulations.
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Resource Material Producer (RMP) Digital Platform

Digitize the production, certification, commercialization, and distribution of certified reference materials.

End-to-End Operational Flow (9 Steps)
1
Demand Planning
Market requirement forecasting, feedstock sourcing, and production scheduling.
2
Production Planning
Target property specification, blending formulas, container selection, and chemist allocation.
3
Batch Creation
Physical batch manufacturing, batch number & barcode generation, and unit packaging.
4
Homogeneity & Stability Studies
Within-bottle and between-bottle testing, short-term transport & long-term storage logging.
5
Value Assignment & Certification (ISO 17034)
Technical review assigning certified property values and expanded measurement uncertainty (k=2).
6
CoA Generation (Dataset Linked)
Certificate of Analysis generated directly from study records, guaranteeing zero data divergence.
7
Catalogue Publication & Commercial Listing
Certified batches published to online storefront with technical specifications and SDS.
8
Customer Ordering, Payment & Reservation
Online ordering, payment gateway confirmation, automated GST invoice, and stock reservation.
9
Logistics, Recertification & Recall Management
Dispatch tracking, periodic stability re-verification, and instant end-to-end recall capability.
Key Capabilities
  • CRM Manufacturing Management: Full batch history, study protocols, and raw data capture.
  • CRM Sales & Distribution: E-commerce portal, shopping cart checkout, and GST billing.
  • Inventory & Order Management: Multi-location inventory visibility and automated stock reserve.
  • Recertification Management: Automated alerts for expiring CRM validity and re-testing.
  • Recall Management: One-click trace from contaminated batch to all recipient customers.
  • Compliance Tracking: Rigorous ISO 17034 and metrological traceability governance.
Business Benefits
  • Increased Revenue Growth: Commercializes BPCL certified reference materials to external labs.
  • Inventory Visibility: Real-time tracking of CRM stock levels, expiry dates, and locations.
  • Improved Fulfillment: Eliminates manual paperwork between order placement and dispatch.
  • Improved Customer Experience: Instant online access to accredited CoAs and batch data.
  • Recall Readiness: Instant containment and automated customer notification.
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ILIMS Module

Provide digital management of laboratory activities while ensuring data integrity, traceability, compliance, and operational efficiency.

End-to-End Operational Flow (9 Steps)
1
Sample Receipt
Receive testing sample with testing requirements, source details, and supporting documentation.
2
Registration & QR/Barcode Assignment
Creation of Digital Sample master record; automated barcode/QR labeling.
3
Storage Allocation & Chain of Custody
Assign lab storage locations (rack/fridge) and track physical movements continuously.
4
Test Assignment
Intelligent allocation to bench analysts based on workload and active competency certifications.
5
Laboratory Testing
Bench analysts perform analysis strictly per approved SOPs displayed on digital workstations.
6
Instrument Integration (IoT Push)
Capture automated readings directly via outbound IoT collectors, eliminating manual typing.
7
Result Validation
Real-time check against product specifications; out-of-specification (OOS) deviations flagged instantly.
8
Review & Approval (Maker-Checker)
Dual-custody verification with cryptographic e-signatures; zero single-user result releases.
9
Report Generation & Archival
Generate tamper-proof Certificates of Analysis (CoA) and permanent storage in WORM storage.
Key Capabilities
  • Sample Lifecycle Management: Comprehensive end-to-end tracking from initial collection through final disposal.
  • Instrument Integration: Direct outbound push architecture.
  • Digital Observation Registers: Audited digital worksheets replacing paper registers.
  • Approval Workflows & eSignature: Cryptographic dual-authorization verification.
  • Audit Logs Management: Complete forensic trail for every result and calculation.
  • Customer Reporting: Automated branded CoA distribution via portal and secure email.
Business Benefits
  • Reduced Turnaround Time (TAT): Eliminates paperwork delays and manual transcription bottlenecks.
  • Improved Productivity: Analysts focus on testing rather than redundant logbook entry.
  • Full Sample Traceability: Instant forensic audit of who tested what, when, and on which instrument.
  • Elimination of Paper Registers: 100% paperless bench operations.
  • Improved Audit Readiness: Full NABL and ISO/IEC 17025 compliance on demand.
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LQMS / QA Portal – Quality, Audit & Smart Lab

A unified quality ecosystem spanning controlled documents, laboratory governance, learning, audits and environmental monitoring.

QA Portal Scope – Three Connected Pillars
Document Management System (DMS)

Controls the creation, approval, publication and acknowledgement of quality content.

Guidelines Quality Manuals QC Circulars Test Methods / Specifications
Quality Management System (QMS)

Orchestrates quality records, equipment readiness, inventory, audits and workforce competence.

Quality Records (QRS) Calibration Stock Audit Training Module Quality Learning Centre
Smart Lab

Adds live facility intelligence to quality operations and sustainability reporting.

Energy Monitoring Water Monitoring Indoor Air Quality Green Initiatives
Controlled Document Management Lifecycle (8 Steps)
1
Document Management & Metadata Assignment
Register and manage SOPs, test methods, circulars, manuals and specifications with structured classification and tagging.
2
Review & Approve Workflow
Multi-level digital review and approval workflow with cryptographic e-signatures.
3
Storage Allocation & Custody Tracking
Central document repository indexing with role-based and geographic access permissions.
4
Publish Documents
Immediate availability of approved revisions across the national laboratory network.
5
Controlled Distribution
Automated push notifications to relevant lab roles, ensuring full operational visibility.
6
Read & Acknowledge
Mandatory digital acknowledgement by analysts before performing associated test methods.
7
Version Control Management
Automated archiving and watermark deprecation ("SUPERSEDED") for older versions.
8
Archival, Retention & Audit Support
Permanent time-locked storage in compliance with NABL multi-year retention mandates.
Key Capabilities
  • Version Control: Strict cryptographic version stamping and change logs.
  • Electronic Workflow: Automated routing, reminder alerts, and escalations.
  • Approval Workflows & eSignature: Multi-tiered authorized sign-offs.
  • Audit Logs Management: Complete history of document reads, prints, and changes.
  • Compliance Reporting: Real-time dashboards of document currency across all labs.
Active Instrument Calibration Interlock (PDF Highlight): If an instrument's calibration lapses, the platform mechanically blocks sample allocation and testing on that device.
Business Benefits
  • Strong Governance: Eliminates unapproved local documentation and shadow spreadsheets.
  • Better Compliance: Continuous adherence to ISO 17025, 17034, and 17043.
  • Easy Document Management: Single central search repository across all national labs.
  • Version Control Capabilities: Guarantees testing is only performed against current standards.
AI Knowledge Assistant (PDF Highlight): In-country Azure OpenAI generative AI provides cited answers strictly from approved SOPs with zero hallucination.
QMS Records & Operational Control
  • Quality Record System (QRS): Structured evidence aligned to ISO/IEC 17025, ISO 17034, ISO/IEC 17043, ISO/IEC 17020 and ISO/IEC 17024.
  • Calibration Module: Plans calibration, maintains certificates and blocks expired instruments from testing.
  • Stock Module: Tracks laboratory stock, TRACE records, disposal of leftover samples and finance-linked controls.
Audit, Quality Learning & Training
  • Audit Module: Plans audits, assigns findings, records evidence and tracks corrective actions to closure.
  • LENS: Provides a focused view of observations, non-conformities and follow-up actions.
  • Quality Learning Centre (QLC): Manages TNI plans, evaluations, Training Effectiveness Index and CAP.
  • Training Module: Assigns role-based learning, conducts lab analyst assessments, records competency outcomes and validates training effectiveness before authorization or requalification.
Closed-loop assurance: Finding → training need → analyst assessment → effectiveness validation → competency approval.
Smart Lab Monitoring
  • Energy Monitoring: Tracks consumption, peaks and efficiency trends by lab or asset.
  • Water Monitoring: Monitors laboratory water usage and exception thresholds.
  • Indoor Air Quality: Captures environmental conditions that may affect people, samples and instruments.
  • Green Initiatives: Converts monitoring data into measurable sustainability actions and reports.
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Risk & Compliance Data Management

Three Pillars of Enterprise Governance, Traceability, and Accreditation Control

1. Regulatory Alignment
  • ISO/IEC 17025:2017: General requirements for the competence of testing and calibration laboratories.
  • ISO 17034:2016: General requirements for the competence of reference material producers.
  • ISO/IEC 17043:2023: Conformity assessment — General requirements for proficiency testing.
  • NABL Compliance: Continuous alignment with NABL 133 and relevant technical guidance documents.
  • India DPDP Act 2023: Complete compliance with India's Digital Personal Data Protection Act.
2. Governance Controls
Access Governance
  • Role-Based Access Control (RBAC)
  • Single Sign-On (SSO) & MFA via Entra ID
  • Segregation of Duties (Maker-Checker)
Process Governance
  • Standardized Digital Workflows
  • Multi-Level Approvals
  • Electronic Signatures (IT Act 2000)
  • Approval Audit Trails with reason codes
Data Governance
  • Single Source of Truth
  • Version Management for all records
  • Master Data Controls
  • Immutable Records (WORM storage)
3. Audit Controls
  • Immutable Audit Trails: Automatic forensic recording of Who, When, Where, What, and Why.
  • Complete Version History: Full chronological lineage for every result, document, and study.
  • Timestamped Activities: Cryptographically verifiable UTC & IST timestamps.
  • Historical Retrieval: Instant retrieval of historical records without affecting live transactional databases.
  • Read-Only Auditor Sandbox: Dedicated time-bound environment for NABL/ISO assessors.
Key Strategic Outcome:

"The Unified QC Platform embeds governance, traceability, and compliance into every transaction, reducing operational risk while improving audit readiness and leadership confidence."

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Phased Delivery Roadmap

Progressive value realization with common platform services established first

Phase Focus / Module Duration Scope Highlights Key Outcome
PHASE 1 PT (Proficiency Testing) 2 MONTHS Scheme management, participant management, sample distribution, ISO 13528 evaluation engine, automated certification. End-to-End PT Digitization
PHASE 2 RMP (Reference Material) 2 MONTHS CRM lifecycle, production tracking, homogeneity/stability study logs, certification, inventory, customer ordering, distribution. Digital CRM Business Platform
PHASE 3 LIMS (Laboratory Information Management) 6 MONTHS Sample lifecycle, testing workflows, digital observation registers, maker-checker approvals, reporting & CoA, instrument integration. Digital Laboratory Operations
PHASE 4 LQMS / QA Portal 4 MONTHS DMS, QRS, calibration, stock and sample-disposal controls, audit and LENS, Quality Learning Centre, lab analyst assessment and training-effectiveness validation, plus Smart Lab monitoring. Connected Quality Governance
PHASE 5 MIS Dashboard for Regional Head 2 MONTHS Leadership dashboards, operational KPIs (TAT), quality KPIs (OOS, CAPA), financial metrics, centralized command center. Quality Intelligence Platform
VALUE REALIZATION MILESTONE: Digital Foundation + ILIMS establishes the reusable core and delivers the first major operational value to refinery and marketing laboratories.
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Program Sizing & Delivery Roadmap

Estimated delivery effort and implementation approach for the Unified QC Digital Platform

PLANNING NOTE: High-level planning estimates; final baseline subject to solution design, requirements validation, integration discovery, and NFR assessment.
16,200
Hours
100% Dedicated Allocation
16
Months
Turnkey Implementation
Solution Sizing Overview (Modules & Efforts)
Modules / Features Efforts (Hours) Proposal Value
PT (Proficiency Testing) 2,200 Hrs ₹ 44,00,000
RMP (Reference Material) 2,200 Hrs ₹ 44,00,000
ILIMS (Laboratory Information) 5,800 Hrs ₹ 1,16,00,000
LQMS (Quality Management) 4,000 Hrs ₹ 80,00,000
Dashboard & Analytics (MIS) 2,000 Hrs ₹ 40,00,000
TOTAL ENTERPRISE PLATFORM 16,200 Hrs ₹ 3,24,00,000
*Shared services (SSO, RBAC, WORM audit, IoT collectors) are apportioned across module efforts.
Delivery Capacity: 12 Core Specialists
Role Team Size Key Responsibilities
Product Owner 1 Product vision, domain analysis, executive alignment, backlog prioritization.
Solution Architecture 1 Cloud architecture (Azure India), microservices, security.
UI/UX Designer 1 Design system, responsive screens, customer portals.
Frontend 3 Next.js / React web applications & dashboards.
Backend 4 NestJS microservices, PostgreSQL, IoT collectors.
QA/Test Engineer 1 Automation, statistical validation (ISO 13528).
TechLead + DevOps 1 CI/CD, Azure Arc edge, WAF, WORM compliance.
TOTAL CORE TEAM 12 Dedicated Turnkey Implementation Squad
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Future-Ready Technology Stack

Best-in-class architecture optimized for high scalability, security, and enterprise performance

Frontend & User Experience
  • Framework: React.js or Next.js for high-performance, dynamic interfaces.
  • State Management: Redux Toolkit / React Query for efficient data caching.
  • UI Library: Tailwind CSS & Headless UI for responsive, accessible, and fast design.
Backend & API Layer
  • Architecture: Microservices-based for independent scaling of modules (PT, ILIMS, etc.).
  • Core Tech: Python (FastAPI) for high-throughput API services.
  • API Gateway: Azure API Management for rate limiting and secure routing.
Data & Storage
  • Primary Database: Azure Database for PostgreSQL for relational integrity and transactional data.
  • Document Store: Azure Cosmos DB (MongoDB API) for flexible schemas.
  • Caching: Azure Cache for Redis to accelerate frequent queries and dashboard metrics.
DevOps, Security & Azure Infrastructure
  • Containerization: Azure Kubernetes Service (AKS) & Docker for automated orchestration.
  • CI/CD Pipelines: Azure DevOps for continuous integration, testing, and deployment.
  • Security: Microsoft Entra ID (Azure AD) for secure SSO, TLS 1.3, and Azure WAF.