The new GMP R&D and production center has high requirements for verification documents. Can your company provide complete verification materials?

Yes. We start with User Requirements Specification (URS) and provide a complete set of validation documents, including Design Qualification (DQ), Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), to ensure that the system successfully passes GMP certification. The Sano Biotechnology project has passed GMP validation in one go.