Pharma & Life Sciences
Manufacturing logic
engineered for
absolute compliance.
Averiq architects pharmaceutical systems where quality control and batch traceability are built into the data layer, not added as an afterthought. We replace operational chaos with institutional governance.
The compliance reality
Fragmented systems in pharma do not just cause delays—they trigger regulatory action.
When formulations are managed in legacy databases, warehouse movement in standard accounting software, and quality checks on paper, the facility operates in a state of high risk.
Averiq consolidates the manufacturing lifecycle. We build an architecture where a failed QC test automatically locks the warehouse dispatch, and every formulation change requires authenticated approval.
Structural weaknesses we eliminate
Batch records maintained on paper, making recall tracing a multi-day crisis
Manual yield calculations leading to hidden material wastage and revenue leakage
Disconnect between QC labs and the warehouse, allowing unapproved stock to be dispatched
Compliance documentation scrambled right before an audit, risking regulatory action
Expiry management handled via spreadsheets, resulting in high write-offs of expired stock
Lack of visibility into vendor quality consistency and historical Certificate of Analysis (CoA) data
Core engineering
The infrastructure for traceable, audit-ready production.
Our systems are not generic ERPs. They are deeply configured for the pharmaceutical domain, enforcing strict operational sequences and immutable record-keeping by default.
Pharma Formulation and Recipe Management
Strict version control for Bill of Materials (BOM). The system locks approved recipes, preventing unauthorized parameter changes while dynamically calculating API potency and yield variances for production scaling.
Pharmaceutical Quality Control and Assurance Software
Mandatory quarantine logic. Raw materials and finished goods are digitally locked until lab test parameters are logged and cleared by authorized QA personnel. No unapproved batch can enter production or transit.
Batch Traceability and Genealogy Software
End-to-end genealogy tracking. Trace any finished product back to the exact raw material supplier, operator, and machine used. Recalls can be executed accurately in minutes, not weeks.
21 CFR Part 11 Compliance ERP
Continuous, immutable audit logging. Every data entry, status change, and approval is recorded with time-stamps and user IDs, ensuring absolute readiness for CDSCO, FDA, or internal compliance audits.
Pharma Warehouse Management System WMS
Warehouse logic engineered for pharmaceuticals. Automated First-Expire-First-Out (FEFO) routing prevents the dispatch of short-expiry stock and alerts management to impending material degradation.
CAPA Management Software
Corrective and Preventive Action (CAPA) tracking integrated directly into the production layer. Deviations trigger automated workflows, ensuring root-cause analysis is completed before subsequent batches are cleared.
Beyond the core
Custom integration for physical operations.
When software needs to bridge the gap into physical hardware and external supply networks, we deploy specialized modules connected directly to the primary ledger.
Track & Trace Serialization
High-speed data ingestion for packaging lines. Generates and tracks unique serial codes across primary, secondary, and tertiary packaging levels to secure the supply chain against counterfeiting.
IoT Environmental Sync
Direct integration with warehouse and production floor sensors. Automatically logs temperature and humidity data into the batch record, flagging any excursions that violate storage parameters in real-time.
Supplier & Vendor Portals
Governed extranets for raw material suppliers. Automates the submission of Certificates of Analysis (CoA) and tracks vendor quality ratings based on historical rejection rates.
Scale & Scope
Architected for the exact node you occupy.
The strict rules of the database remain constant, but the application is molded to fit the operational reality of your specific tier in the life sciences chain.
Primary & Secondary Manufacturers
Full-scale formulation governance, continuous quality monitoring, and machine-level batch tracking for API and finished dosage production.
Contract Manufacturing Organizations (CMOs)
Multi-client data segregation, flexible production line scheduling, and client-specific audit report generation.
C&F Agents and National Distributors
High-volume warehouse management, strict FEFO dispatch logic, and track-and-trace compliance across regional distribution nodes.
R&D and Analytical Testing Labs
Sample lifecycle management, analytical instrument data logging, and strict documentation version control for research phases.
Technical Validation
Critical protocol questions.
Initiate Assessment
Audit your operational logic.
We begin by mapping out your current formulation workflows and identifying compliance gaps in your existing data architecture.