At Interphex 2009 in New York,US Outsourcing-pharma spoke with industry expert Jennifer Riter of West Pharmaceutical Services about the scope of the CFR-21 parts 210 and 211 as they apply to microbiology, de-pyrogenation processing and batch closure regulations.
Riter also talked about how well the pharmaceutical industry has adapted to the new good manufacturing practice (GMP) standards and explained how West can help its customers understand and comply with the rules with its line of ready-to-steralise components.