Adents is a leading provider of premier serialization solutions for unique product identification and traceability. Adents helps pharmaceutical companies, Contract Manufacturing Organizations (CMOs) and their Supply Chain Partners adapt to market changes and comply with regulations on drug traceability.
With its two serialization solutions, Adents Seriza (for manufacturing sites), and Adents Prodigi (for marketing authorization holders), Adents is differentiating itself through several crucial factors:
•Permanent compliance: Adents offers the only fully configurable serialization solutions, ensuring compliance with current regulations as well as future regulatory requirements.
•End-to-End data management: Adents has deployed a global serialization solution from Level 2 through Level 5 for its customers. This gives Adents unique expertise on the serialization data lifespan, from initial generation and exchange with supply chain partners allthe way through reporting or sharing with local authorities and governments.
•Widest connectivity: Because of Adents Prodigi, a cloud-native solution co-developed with Microsoft, Adents became the first European provider to offer a certified Gateway to the EMVS (European Medicines Verification System). Having joined the pilot program, Adents is in the process of connecting Prodigi with the Russian Hub. Furthermore, the integration with Origin, a central data repository in the US operated by the Healthcare Distribution Alliance (HDA), is underway.
•Global network of serialization experts: Along with highly respected partners such as Microsoft and Siemens, Adents offers the only global network that keeps on growing. This network consists of more than 800 experts eager to ensure fast and seamless implementation of Adents solution.
Adents operates globally, with offices in the United States, Europe and Asia.

Cold Chain Technologies (CCT) is the trusted global leader of innovative thermal packaging solutions that protect the integrity of temperature-sensitive products. The company offers a complete line of cost-effective thermal packaging products and services, including off-the-shelf and custom KoolTemp® insulated containers and GTS pre-qualified shipping systems, Koolit® refrigerants and advanced phase change materials (PCMs) and temperature indicators and data loggers. For more than 45 years, Cold Chain Technologies has been ensuring product safety with the industry's smartest solutions.

Since it was founded in 1996, Elitech has been dedicated to R&D and manufacturing of cold chain products and management solutions for the freezing and refrigeration industry. With more than 170 R&D engineers and its own manufacturing facility, Elitech has the ability to provide customers a cutting-edge, cost-effective and competitive tailored solution to meet their cold chain needs. Elitech owns more than 80 authorized patents with 30 of them in cold chain software. A company-owned, cloud-based platform allows customers to access real-time data from anywhere, anytime with comprehensive alarm settings.

Origin is a high-powered database designed to be a master list of product Global Trade Item Numbers (GTIN). It eliminates the need for all pharmaceutical supply chain stakeholders to reference multiple sources of data, and the system assists with barcoding compliance and data exchange guidelines set forth by DSCSA. Origin participants have around-the-clock access to a cloud-based portal to exchange master data between manufacturers and their trading partners to ensure safe and efficient product movement through the supply chain.

In response to industry demands, Legisym is preparing the 2018 launch of License Verify^™ – a NEW comprehensive service for verifying pharma licensing across the nation. The same trusted partner who changed the paradigm of Controlled Substance Ordering System (CSOS) with the 100 percent web-based solution Express222™, continues to raise expectations of regulatory compliance partnerships. With affordable and effective services and solutions based on a client’s specific business needs and feedback, Express222^™ enables manufacturers, wholesalers, distributors, health systems and other suppliers to securely process electronic controlled substance orders with real-time DEA compliance. Without expensive hardware and software installation, Express222^™ is device and browser agnostic while automatically scaling to meet demands.

Soon through License Verify™, the same license information suppliers collect through manual, time-consuming searches of multiple state and federal data sources, will be instantly verified and available through a single, comprehensive database. After the initial pilot, Legisym anticipates expansion to include a number of other license types based on industry need.

MedPro Systems^® is the leading provider of healthcare license solutions to the life science industry. The MedProID^® suite of products assists pharmaceutical & device manufacturers, distributors and other healthcare organizations with practitioner and organization state license validation solutions to meet Aggregate Spend, DSCSA/DQSA and Prescription Drug Marketing Act (PDMA) compliance requirements. The foundation of MedProID^® is a comprehensive 21 million record database of practitioner and organization licensing information obtained directly from over 800 state licensing authorities, which is cross-referenced with additional industry data sources and identifiers. MedPro’s solutions are used by more than 450 customers, including 21 of the Top 25 pharmaceutical manufacturers.