(Logo: http://photos.prnewswire.com/prnh/20090824/FDALOGO)
(Logo: http://www.newscom.com/cgi-bin/prnh/20090824/FDALOGO)
The ISO/IEC 17025 is a standard developed by the International Standards Organization (ISO) and the International Electrotechnical Commission (IEC) to merge requirements for technical competence in testing and calibration laboratories with requirements for quality systems.
CBER received accreditation for six methods to test influenza vaccines, including those for sterility and potency, and seven methods for evaluating blood donor screening kits that detect the presence of HIV, HBV, HCV, HTLV-I/II, Trypanosoma cruzi, and West Nile virus. These laboratory activities have a direct impact on regulatory decisions. The Laboratory Quality System program supports the development and evaluation of national reference materials and standards, as well as evaluation of manufacturers' assays.
Accreditation of CBER's Laboratory Quality System provides additional transparency and acknowledgement of a program that has been recognized as an international leader in biological products regulation.
For more information:
About the International Standards Organization
http://www.iso.org/iso/about.htm
About the International Electrotechnical Commission
http://www.iec.ch/helpline/sitetree/about/
Visit the FDA on Facebook and Flickr
Media Inquiries: Shelly Burgess, 301-796-4651, shelly.burgess@fda.hhs.gov
Inquiries: 888-INFO-FDA
SOURCE U.S. Food and Drug Administration