Digitize your production, quality, and regulatory workflows in Dubai with a unified platform built for formulations, API, and sterile manufacturing. Built for trust.
Pharma manufacturing is the most regulated industry globally. Paper-based systems are no longer viable for modern facilities in Dubai facing rigorous FDA, WHO, and local GMP audits.
Manual logs are prone to data integrity issues. Zymofar's bank-grade electronic audit trails track every single entry, edit, and signature for 100% inspection-ready status.
Tracing a raw material lot to an individual patient packet manually takes days. Our system does it in seconds, enabling lightning-fast precision recalls.
Integrated LIMS (Laboratory Information Management) ensures no batch hits the market without passing 100% of validated quality checkpoints.
Validated metrics from FDA-approved manufacturing units.
Modular compliance architecture specifically engineered for the high-precision requirements of Life Sciences.
Manage electronic batch manufacturing records (EBMR), multi-stage formulations, and master formula control with integrated weighing scales and BMR logging.
Integrated CAPA, Deviations, Stability Studies, and LIMS for real-time certificate of analysis (CoA) generation. Built-in lab equipment integration.
Full batch genealogy tracking from raw API to finished pack. GS1-standard serialization support for global "Track & Trace" export compliance.
Unforgeable electronic audit trails. Tracks who, when, and where of every transaction with mandatory dual-level electronic signatures and versioning.
Instant batch recall and vendor qualification modules. Fully integrated with serialization for secure distribution and market surveillance.
Automated pharmaceutical regulatory reporting, GST/VAT compliance, and detailed batch-level costing with manufacturing overhead analytics.
Incoming API testing with automated quarantine-to-approved status and GRN-linked batch logging.
Precision dispensing with integrated weighing scales and mandatory BMR second-level verification.
Laboratory assay tests and final CoA generation before system-enforced market release.
Applying unique aggregate identity codes for global "Track & Trace" distribution security.
From neighborhoud API units to global sterile manufacturing chains, our architecture adapts to your compliance DNA in Dubai.
The only pharmaceutical ERP that guarantees "Inspection Readiness" with real-time audit trail encryption.
Schedule a compliance-focused walkthrough with our Life Science consultants today.