Looking for a superior GxP solution for your pharmaceutical or R&D laboratory? TRANSCEND™ Digital Suite is transforming the industry by enabling real-time, paperless data management with full GMP compliance.
Our platform supports seamless, bi-directional data synchronisation with existing LIMS, MES, SAP, and QMS systems—eliminating manual data entry, ensuring data consistency, and safeguarding data integrity. Lab analysts can now generate and manage data in real time, streamlining workflows and boosting efficiency.
TRANSCEND™ Digital Suite is fully compliant with US, EU, and China regulations, including CFR 21 Part 11 standards. The system’s universal compatibility with 99% of lab and production equipment makes it ideal for both new and legacy environments, supporting digital transformation without costly upgrades.
Experience the power of automated data capture, integrated reporting, and robust compliance—all in one platform. Say goodbye to paper logbooks and manual processes. Say hello to the future of digital pharma.
Reach out to Oasis Biotechnologies & Service Pte Ltd (ksisoh@oasisbiotechs.com.sg) to learn more about TRANSCEND™ Digital Suite.
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