4 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform ISO 11737-2 testing. From the accredited scope text: “ISO 11737-2; USP<71> Microbial Enumeration Testing for Specified Microorganisms USP <61>; USP <62>; USP <1111> EP/BP Testing Activities performed under the scope of the U.S FDA ASCA Pilot Program Spec” “ISO 11737-2, EN ISO 11737-2 P-0004, P-0006, P-0009” “ISO 11737-2/ USP <71> Q08-WI-002545 Sterility Test ANSI/AAMI/ISO 11737-2/ USP <71> Q08-WI-002550 Q08-WI-002551 Endotoxin: Gel Cot Method AAMI ST72/ USP <85>, <161> ISO 11737-3 Q08-WI-002543 Kinetics M” “ISO 11737-2, USP <71> Q08-WI-002722 Recovery Efficiency Test ANSI/AAMI/ISO 11737-1 Q08-WI-002719 Sterility Test ANSI/AAMI/ISO 11737-2, USP <71> Q08-WI-002709”
Hercules, CA, US
ISO 11737-2; USP<71> Microbial Enumeration Testing for Specified Microorganisms USP <61>; USP <62>; USP <1111> EP/BP Testing Activities performed under the scope of the U.S FDA ASCA Pilot Program Specifications: Biocompatibility Te
Acton, MA, US
ISO 11737-2, EN ISO 11737-2 P-0004, P-0006, P-0009
Brooklyn Park, MN, US
ISO 11737-2, USP <71> Q08-WI-002722 Recovery Efficiency Test ANSI/AAMI/ISO 11737-1 Q08-WI-002719 Sterility Test ANSI/AAMI/ISO 11737-2, USP <71> Q08-WI-002709
El Paso, TX, US
ISO 11737-2/ USP <71> Q08-WI-002545 Sterility Test ANSI/AAMI/ISO 11737-2/ USP <71> Q08-WI-002550 Q08-WI-002551 Endotoxin: Gel Cot Method AAMI ST72/ USP <85>, <161> ISO 11737-3 Q08-WI-002543 Kinetics Method AAMI ST72/ USP <85>,
This page is a fixed slice of the register: every ISO 11737-2 scope we hold for United States. Search narrows it further by city, accreditation body, or a term from the scope text itself.
Search labs in United StatesAmerican Association for Laboratory Accreditation (A2LA) is the primary accreditation body issuing ISO/IEC 17025 accreditation for testing laboratories in United States.
ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. Accreditation to this standard provides independent confirmation that a laboratory operates a quality management system and is technically competent to produce valid results within its declared scope.