Tatmeen

Revolutionizing Pharmaceutical Security: UAE's Tatmeen Traceability System

UAE's Tatmeen Traceability System

The United Arab Emirates has positioned itself as a regional leader in pharmaceutical security through the implementation of one of the world's most advanced drug traceability systems. Spearheaded by the Ministry of Health and Prevention (MOHAP), the UAE's comprehensive regulatory framework centers around the Tatmeen platform—a sophisticated digital ecosystem designed to ensure complete transparency and security across the pharmaceutical supply chain. This cutting-edge approach not only safeguards patient welfare but also establishes the UAE as a benchmark for pharmaceutical regulatory excellence in the Middle East.

Key Pillars of UAE's Pharmaceutical Traceability Framework

Mandatory Product Serialization and Digital Identity

The UAE requires every pharmaceutical product to carry a unique serialized identifier encoded in a GS1 DataMatrix barcode on secondary packaging. This digital fingerprint includes critical data elements such as the Global Trade Item Number (GTIN), randomized serial number, expiry date, and batch information. This granular identification system enables precise tracking of individual units throughout their entire lifecycle, from manufacturing facilities to patient dispensing, creating an unbreakable chain of custody that effectively prevents counterfeit products from entering the legitimate supply chain.

Centralized Real-Time Monitoring Through Tatmeen

The Tatmeen platform serves as the nerve center of UAE's pharmaceutical oversight, functioning as a centralized repository that captures and verifies all product movement data in real-time. This sophisticated system empowers regulatory authorities to monitor product status continuously, facilitate rapid recalls when necessary, and prevent the distribution of expired or fraudulent medications. All supply chain participants—from manufacturers and distributors to pharmacies and hospitals—must integrate with Tatmeen, ensuring comprehensive visibility across every touchpoint in the pharmaceutical distribution network.

Comprehensive Packaging Hierarchy and Aggregation Management

UAE regulations mandate meticulous documentation of packaging hierarchies, requiring clear identification of relationships between individual units, bundles, cases, and pallets. Aggregated packaging must display serialized identifiers, typically using Serial Shipping Container Codes (SSCC), while maintaining traceability connections throughout the supply chain. This systematic approach ensures that even when products are repackaged or redistributed, their authenticity and chain of custody remain intact, providing regulators with complete visibility into product movements at every level of packaging.

Standardized Data Reporting and Compliance Framework

The regulatory system requires all operational and transactional movements to be recorded and reported to Tatmeen using standardized EPCIS message formats in chronological order. This includes manufacturing events, importation activities, aggregation processes, distribution movements, and final dispensing transactions. Supply chain stakeholders must register with GS1 UAE to obtain Global Location Numbers (GLN), ensuring standardized identification across the ecosystem. The framework includes specific compliance deadlines, with all products imported or produced after December 2021 required to meet serialization and reporting requirements.

Why Choose Our iTS Compliance Solution

Expert Guidance

Our team of compliance experts possesses in-depth knowledge of iTS and Turkish pharmaceutical regulations. From serialization strategies to data reporting, we guide your organization through the intricacies of compliance, ensuring a smooth and informed journey.

Cutting-Edge Technology

Leverage our state-of-the-art compliance solution, designed to integrate seamlessly with iTS requirements. Our technology ensures accuracy, efficiency, and real-time visibility, empowering your organization to meet and exceed compliance expectations.

Future-Ready Operations

Compliance is not just about meeting today's standards; it's about preparing for the future. Our solution is designed to evolve with regulatory changes, ensuring that your organization remains at the forefront of compliance in the dynamic Turkish pharmaceutical landscape.

Transparent Collaboration

We believe in transparent collaboration. Partner with us, and we'll work closely with your team to implement and maintain compliance measures. Our goal is to build a resilient, compliant, and future-ready pharmaceutical supply chain together.

Speak With a Compliance Expert

Empowering UAE Pharmaceutical Compliance with LSPedia Solutions

Navigating the UAE's sophisticated Tatmeen traceability requirements demands specialized expertise and robust technological capabilities. LSPedia offers comprehensive solutions specifically designed to help pharmaceutical organizations achieve seamless compliance with UAE regulations. Our platform provides end-to-end serialization management, automated Tatmeen integration, and real-time compliance monitoring, ensuring your operations align perfectly with MOHAP requirements. From initial product registration support to ongoing aggregation management and standardized EPCIS reporting, LSPedia's proven expertise transforms complex regulatory challenges into streamlined operational advantages, enabling pharmaceutical companies to focus on their core mission of delivering safe, authentic medications to UAE patients while maintaining full regulatory compliance.

Get In Touch

We invite you to learn more about how LSPedia can support your compliance and supply chain needs. For more information about our solutions, partnership opportunities, or to speak with one of our experts.

Contact Us

Stay connected with us on social media and subscribe to our newsletter to receive the latest updates, insights, and innovations from LSPedia.