The GMP-Ready Workflow Platform for Pharma Manufacturing
From Active Pharmaceutical Ingredients (APIs) to finished formulations, FlowMaster provides end-to-end traceability and control over your entire manufacturing lifecycle. Unify your sales, quality control, production, and dispatch teams on a single, compliant platform.
Maintain an Audit-Ready, Single Source of Truth
Our centralized masters ensure consistency and control from start to finish.
Customer & End-Customer Master
Manage detailed profiles for all clients, including TPM partners and their end customers, complete with Drug License and GSTIN details.
Product & Raw Material Master
A unified repository for all finished goods, APIs, excipients, and packaging materials. Specify grades, suppliers, and shelf life.
Bill of Materials (BOM) Master
Digitally define and lock your master formula for every product, ensuring precise material dispensing for every batch.
Effortless Data Portability
Securely import and export master data using pre-formatted Excel templates, perfect for audits and system migrations.
Transform Enquiries into Production Orders
Our workflow captures every critical detail and maintains a complete digital paper trail.
Detailed Enquiry Capture
A pharma-specific form to document everything from formulation requirements and dosage forms to custom packaging and regulatory label compliance.
Seamless Deal Conversion
A robust approval process converts a finalized enquiry into a locked-down "Deal" or production order, automatically triggering pre-production checks.
Live Order Tracker
Gain real-time visibility into every order's progress through store checks, design approvals, quality control, and production scheduling.
Connect Every Department on a Single Platform
FlowMaster is designed to meet the rigorous demands of pharmaceutical manufacturing by uniting your entire workflow.
Leverage Your Data for Quality and Growth
Drive quality improvements and stay prepared for regulatory audits with powerful, built-in reporting.
Analyze the profitability of each product batch to understand your true costs and margins.
Track performance by sales executive, product, or region to identify key growth areas and opportunities.
Generate reports that trace a finished product all the way back to the raw materials used.
Built for a Regulated World
In the pharmaceutical industry, compliance isn't optional—it's the foundation of your business. FlowMaster is designed with a deep understanding of GMP principles and the need for robust data integrity.
Digital Batch Records
Move away from paper-based BMRs. Our system generates detailed, consistent, and error-resistant batch records for every production run.
Complete Audit Trail
Every significant action is logged with user and timestamp details, providing a clear and comprehensive audit trail.
Version Control
All changes to critical documents like BOMs and packaging designs are versioned, ensuring you always have access to historical records.
Role-Based Access Control
A granular permissions system ensures that team members can only access and modify information relevant to their roles.
21 CFR Part 11 Ready
Our platform provides foundational features, including electronic signatures and secure audit trails, to help you meet FDA requirements.
Empowering Pharmaceutical Excellence
At FlowMaster, our mission is to provide pharmaceutical manufacturers with the digital tools they need to thrive in a competitive and highly regulated environment. We were founded by industry veterans who grew tired of disconnected spreadsheets, paper-based records, and the constant struggle to maintain a single source of truth.
We believe that true operational excellence comes from a seamlessly integrated workflow where data flows as smoothly as your production line. FlowMaster is more than just a CRM; it's a commitment to quality, compliance, and efficiency.
Ready to Achieve Manufacturing Excellence?
Bring compliance, control, and clarity to your pharmaceutical manufacturing operations. Schedule a demo to see how FlowMaster can transform your workflow.