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Chetu's ERP software developers create custom programs for managing and standardizing enterprise-wide pharmaceutical development processes and promoting lean, continuous manufacturing operations. Our pharmaceutical ERP systems cover all process areas, including formulation, material acquisition, production, QA, and distribution. We integrate Laboratory Information Management Systems (LIMS) with dynamic process schedules, automation control centers, and secure formula management protocols.
We develop batch processing software and Material Requirements Planning (MRP) modules for managing all drug manufacturing processes, including temperature mapping, extraction, synthesis, fermentation, proportioning, milling, API and excipient blending, granulation, freeze-drying, hot melt extrusion, cleaning, and packaging. We program pharmaceutical inventory management software with serial and lot number tracking databases and network equipment management software to track real-time performance.
We program procurement and distribution management platforms that support supply chain visibility of materials by seamlessly networking with courier and client tracking systems. We integrate programs for inventory control, order procurement, warehouse management, shipping management, and reverse logistics. We facilitate more accurate, reliable distribution of products by programming sales platforms with Available-to-Promise (ATP) functions and inventory databases with multiple Units of Measure (UoM).
Our Quality Management Systems (QMS) optimize QA and expand traceability, and our collaborative Material Review Board (MRB) programs enable users inside and outside of the production company to track component discrepancies. We integrate modules for managing standard operating procedures (SOP), complaints, audits, and regulatory documentation. We also program automated nonconformance alerts, risk assessment tools, and Corrective and Preventative Action (CAPA) protocols.
We implement scalable Electronic Batch Records (EBR), often utilizing modern batch frameworks like Spring and Java Batch. Our EBR systems track processes, workflows, user interactions, and deviations in real time and upload all data to a central repository for further analysis. Our Bill of Materials (BOM) modules archive product materials and formulas, compliant with the FDA's 21 CFR Part 211. We program Engineering Change Order (ECO) modules with automated, multi-tiered approval requests and one-click confirmations
We integrate pharmaceutical CRM systems for managing relationships with clients and manufacturing partners and for handling marketing and lead acquisition. We integrate work order management and accounting systems in order to centralize financial operations, including Sales Expense Tracking and Management, in accordance with the Physician Payments Sunshine Act. We program pharma project management software that offers extensive budget tracking of R&D, marketing, and other development costs.
Chetu's software solutions compliant with Food and Drug Administration (FDA) requirements such as Current Good Manufacturing Practices (cGMP), Title 21 Code of Federal Regulations Part 11 (21 CFR Part 11), and National Drug Codes (NDC). Our software also meets regulations put forth by the National Council for Prescription Drug Programs (NCPDP), United States Pharmacopeia (USP), and the U.S. Department of Health and Human Services (HHS)
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1500 Concord Ter.
Suite 100,
Sunrise, FL 33323
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