Global Leaders in Commissioning, Qualification & Validation
Helping biotech and pharmaceutical organisations build and validate compliant GMP facilities—on time, on budget, and inspection-ready from day one.

Who are Zyme Biotech?
Zyme Biotech is a global leader in Commissioning, Qualification & Validation (CQV), backed by a team of specialists and more than a decade of hands-on experience.
Our strength lies in translating strategy into execution, delivering inspection-ready facilities, optimizing validated processes, and ensuring seamless regulatory compliance.This approach enables our partners to achieve measurable performance, operational excellence, and sustained GMP readiness.
Specialized CQV Knowledge
Our team combines deep expertise across Commissioning, Qualification & Validation (CQV), GMP compliance, and biotech project delivery. From facility design through performance qualification, we provide the technical insight needed at every stage of your project lifecycle.
Global Delivery Experience
With on-the-ground experience across Europe, the GCC, and the US, our experts apply global GMP standards and local regulatory knowledge to every engagement, delivering inspection-ready outcomes for leading biotech and pharmaceutical companies.
Adaptive Project Integration
We scale our capabilities to match your project’s demands, seamlessly integrating additional expertise into our core CQV teams. This flexible, collaborative model ensures you always have access to the right specialists, exactly when and where you need them.
AI solution provider and integrator specialising in the biotech sector. Leveraging advanced AI technologies to enhance pharmaceutical manufacturing. Dedicated to innovation, AI-driven tools streamline complex processes, enhance decision-making, and automate knowledge work, ensuring operational excellence.
BioEra works in cooperation with global strategic partners in the fields of project management, engineering work for pharmaceutical factories, scientific and operational consulting for biopharmaceutical industries, business development, artificial intelligence applications, e-marketing and application design. in Riyadh, Kingdom of Saudi Arabia.
ServBlock specializes in applying blockchain technology to secure and streamline pharmaceutical supply chain processes, ensuring transparency and efficiency. ServBlock’s secure and transparent platform is designed to address the unique challenges faced by the pharmaceutical industry, enabling end-to-end traceability.
Setting the electronic validation standard for 20 years, ValGenesis Validation Lifecycle Management System (VLMS) provides unparalleled power, capability, and flexibility to enable 100% paperless, risk-based validation.
Connect design, qualification and production with the unified digital platform for life sciences.
Connect design, qualification and production with the unified digital platform for life sciences.





.png)

