Oligonucleotide Manufacturing Process Development
Analytical Methods
& Stability Study
Manufacturing for Clinical Phases
Manufacturing for Commercial Phases
Preparation, aseptic filling or
Validation & Quality

Improve Validation Procedures

The consistency and repeatability of manufacturing are the key indexes for nucleic acid drug production. RiboBio has established a series of validation procedures to meet the internationally accepted GMP standards, which includes:

● Validation of Facility and Public Utilities
●  Equipment Validation
●  Validation of Analytical Method
●  Process Validation
●  Cleaning Validation
●  Validation of Computer and Automatic System
●  Technician Validation

Guangzhou RiboBio Co., Ltd.
Address:13-14/F, Innovation Building C3, 182 Kexue Avenue, Science Park
Guangzhou 510663, China
Service hotline:400-686-0075

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