About Us
PharmaIQ is an advanced, AI-powered Enterprise Resource Planning (ERP) system purpose-built for the pharmaceutical industry. Designed to streamline the complex operations of pharmaceutical R&D, manufacturing, quality control, regulatory compliance, and supply chain management, PharmaIQ integrates cuttingedge artificial intelligence to deliver intelligent automation, predictive insights, and compliance-driven workflows.
Core Modules
Production Planning
- Material Requirement Planning
- Master Production Scheduling
- Production Process Definition
- Demand Management
- Batch Manufacturing Practice
- Raw Material Formulation
- Packing Material Formulation
- Material Planning
Inventory Management
- Inventory Planning
- Warehouse Management
- Bin Management
- Material Inward / Outward
- Physical Stock Verification
- Physical Stock Verification
- Stock Costing and Valuation
Material Management
- Raw Material Indent
- Packing Material Indent
- Raw Material Issue
- Packing Material Issue
- Return Raw Material
- Return Packing Material
- Quality Assurance
Sales & Procurement
- Supplier/ Vendor Management
- Product Delivery & tracking
- Quote to Receipt Management
- Integration with Planning
- Customer Management
- Sales Management
- Reduce Forecasting Errors
Purchase Management
- Supplier Evaluation
- Request for Quote
- Quote Comparison
- Order Calling
- Purchase Budget and Approval
- Integrated with Planning Function
- Supplier Order Management
Quality Control
- Raw Material Testing
- Bulk/ Finish Goods Testing
- Release Order
- Transfer Slip
- Tag Printing
- Rejection Order
- Testing Req. Slip
Finance & Accounting
- General Ledger, Accounts Payable, Receivables
- Trial Balance, Cash Flow
- Debit Note/ Credit Note/ Cost
- Automatic TAX Calculation
- PDC & Outstanding
Quality & Compliance Management
- FDA Compliant
- Quality Analysis and Control
- Pre-process, Inprocess, Post-Process
- Inventory & Stock QC
- Lot movement as per GMP
- Labels, MBR, BMR, SOPs and COA generation
- Stability Testing, NC,CAPA and Adverse Event Reporting
Reporting
- Production Register
- Consolidate Register
- Yield Register
- Packing Not Issue
- Sample RegisterBulk/finish/Raw
- Control Sample Register
- Transfer register
Key Benefits
Regulatory Compliance Made Easy
- All core hospital dFDA 21 CFR Part 11
- GMP, GLP, GCP
- WHO, EMA, CDSCO compliant with unified, secure hospital system.
Complete Batch & Lot Traceability
- Recalls
- Regulatory audits
- Quality investigations
Integrated Quality Control & Assurance
- Automated inward, in-process, and final quality checks
- CAPA and deviation tracking
- SOP and CoA management Build a quality-first culture across your organization.
Powerful Manufacturing Management
- BMR/BPR automation
- Formulation control (BOMs)
- Yield analysis
- Equipment calibration tracking
- Batch validation and costing
Real-Time Inventory & Warehouse Control
- Live inventory updates
- Multi-location & cold-chain warehouse support
- Expiry & re-test alerts
- Barcode/RFID integration
Smarter Procurement & Vendor Management
- Approved vendor list (AVL) enforcement
- Supplier audit logs
- Purchase planning based on actual demand
- Quality-based supplier rating
Built for Pharma, Not Generic
- BMR/BPR automation
- Formulation control (BOMs)
- Yield analysis
- Equipment calibration tracking
- Batch validation and costing
Executive Dashboards & Custom Reports
- KPI dashboards (OTIF, yield %, rejection rate)
- Regulatory and financial reports
- Customizable analytics by role or department
Role-Based Security & Audit Logs
- User-level access control
- Encrypted logins
- System-wide audit trails for 21 CFR Part 11 compliance
Request a call back
Would you like to speak to one of our advisers over the phone? Just submit your details and we’ll be in touch shortly. You can also email us if you would prefer.
I would like to discuss:
Industries we covered
Biotechnology
Vaccines
Dietary
Veterinary
API
Nutraceuticals
AI-POWERED FEATURES
It refers to the integration of artificial intelligence technologies into the pharmaceutical industry to improve drug discovery, development, manufacturing, supply chain, and patient outcomes.
Predictive demand planning
Predictive demand planning in PharmaTech uses AI and data analytics to forecast product needs, optimize inventory, reduce waste, support compliance, and improve patient access to medications and technologies.
Anomaly detection in quality data
Anomaly detection in quality data identifies deviations from normal patterns in pharmaceutical manufacturing, helping detect defects, process issues, or data integrity problems early to ensure compliance and safety.
Smart reordering and inventory optimization
Smart reordering and inventory optimization use real-time data and AI to automate stock replenishment, reduce excess inventory, prevent stockouts, and improve efficiency across the pharmaceutical supply chain.
AI Chatbot for internal queries
An AI chatbot for internal queries streamlines employee support by instantly answering HR, IT, compliance, and operations questions, improving productivity, reducing response time, and ensuring consistent information across teams.
Intelligent alerts and compliance reminders
Intelligent alerts and compliance reminders use AI to notify staff of critical deadlines, regulatory updates, or process deviations, ensuring timely actions, reducing risks, and maintaining regulatory compliance in PharmaTech operations.
Real-time KPI dashboards
Real-time KPI dashboards provide live visibility into key performance indicators across production, quality, and supply chain, enabling faster decision-making, proactive issue resolution, and improved operational efficiency in PharmaTech.
Things You Get
Our Expertise
Working with our certified experts means you get tailored, high-quality solutions, delivered on time and within budget. We ensure seamless collaboration, leveraging industry-best practices to bring your vision to life with efficiency and reliability.