Jordi Labs offers advanced regulatory testing services on a continuous or contract-based capacity, helping customers meet stringent quality control standards. Our expert team of Ph.D. chemists is experienced with a wide range of sector-specific test methods. This empowers us to provide reliable and repeatable results for businesses in highly-regulated industries such as the pharmaceutical market. We help researchers and developers (R&D) in pharma industries with tried-and-tested U.S. Pharmacopeia (USP) compendial testing services.
The USP is an authority in quality control and regulation of pharmaceuticals, and one of the longest standing pharmaceutical conventions worldwide. Adhering to USP specifications requires rigorous testing and product evaluations to guarantee the quality of pharma products for national and global markets.
At Jordi Labs, we specialize in USP compendial testing where the primary objectives focus on particulates, residual solvents or elemental impurities. Particulates and residue testing is one of our core competencies and we place tremendous importance on our ability to detect subvisible contaminants in purity-critical products. We also routinely carry out procedural elemental impurities testing and limit establishment according to USP 233 and USP 232 respectively.
Browse the table below to see a full list of the USP testing specifications that we are well-versed in or contact a member of the Jordi Labs team today if you have any questions about our regulatory testing services.
|USP 787||USP||Subvisible Particulate Matter in Therapeutic Protein Injections|
|USP 788||USP||Particulate Matter in Injections|
|USP 789||USP||Particulate Matter in Ophathalmic Solutions|
|USP 661||USP||Plastic Packaging Systems and Their Materials of Construction|
|USP 232||USP||Elemental Impurities -- Limits|
|USP 233||USP||Elemental Impurities -- Procedures|
|USP 467||USP||Residual Solvents|
|USP 661.2||USP||Plastic Packaging Systems for Pharmaceutical Use|
|USP 661.3||USP||Plastic Components and Systems Used in Pharmaceutical Manufacturing|
|USP 671||USP||Containers—Performance Testing|
|USP 40-NF 35||USP||Validation of Compendial Procedures|