Strict Adherence to Quality Assurance

Ryss Lab follows accepted industry standards and practices for general laboratory work. Records are faithfully generated and carefully stored, and our technicians conscientiously follow all established Standard Operating Procedures (SOP).

As well, Ryss Lab will follow the federal Food and Drug Administration (FDA) guideline of current Good Manufacturing Practices (cGMP) to produce active pharmaceutical ingredients (API) and products for clinical trials. Our Taiwan facility is fully aware of the new FDA IHC Q7A guideline for API manufacturing.

Separate Quality Assurance/Quality Control (QA/QC) personnel maintain an effective system of checks and balances.

Industry-Leading Quality Control

Prior to release, our independent QC Department will certify product purity to ensure that your exact specifications are met. Purity is usually checked using HPLC, NMR, MS, Melting Point, and other analytical procedures.
Example of Fmoc-Gla(di-butylester)-OH