{"title":"cGMP for the Quality Control Laboratory","description":"\u003cp class=\"header-block-grey\"\u003eCourse Description\u003c\/p\u003e\n\u003cp\u003eThis\nweb seminar will provide a general overview of the cGMP regulations that are\napplicable to a quality control (QC) laboratory following ICH guidelines and 21\nCFR 211. We will discuss the requirements for lab equipment, such as\ncalibration, maintenance, and validation, as well as review analytical method\nvalidation, reference standard qualification, and documentation practices. This\nweb seminar will also cover regulatory requirements for stability testing per\n21 CFR 211.166 and ICH Q1. The session will conclude with a discussion around\nthe requirements of proper Out of Specification (OOS) investigation. \u003c\/p\u003e\n\u003cp class=\"header-block-grey\"\u003eLearning Objectives\u003c\/p\u003e\n\u003cul type=\"disc\"\u003e\n\u003cli\u003eReview the requirements of laboratory equipment,\n     including calibration, preventative maintenance, and validation\u003c\/li\u003e\n\u003cli\u003eReview the requirements of\n     analytical method validation, reference standard qualification, and\n     general documentation practices\u003c\/li\u003e\n\u003cli\u003eDescribe the regulatory requirements\n     of stability testing\u003c\/li\u003e\n\u003cli\u003eDescribe the requirements of\n     investigating OOS test results\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp class=\"header-block-grey\"\u003eWho Should Attend\u003c\/p\u003e\n\u003cul type=\"disc\"\u003e\n\u003cli\u003eQuality Control Staff\u003c\/li\u003e\n\u003cli\u003eLab Management\u003c\/li\u003e\n\u003cli\u003eLab Analysts\u003c\/li\u003e\n\u003cli\u003eQuality Assurance Staff\u003c\/li\u003e\n\u003cli\u003eProduction Personnel\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp class=\"header-block-grey\"\u003eInstructor\u003c\/p\u003e\n\u003cp\u003eSusan\nM. Leister, M.B.A., Ph.D., CQA, CSSBB\u003c\/p\u003e\n\u003cp\u003e\u003cspan class=\"purple-link\"\u003e\u003cspan\u003e\u003ca href=\"https:\/\/stage.barnettinternational.com\/instructor-biographies\" title=\"Click here for complete trainer biographies\"\u003e\u003cspan\u003eClick here for complete trainer\nbiographies\u003c\/span\u003e\u003c\/a\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"header-block-grey\"\u003eRegistration Fees\u003c\/p\u003e\n\u003cp\u003e$835\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIncludes up to 20\nparticipants at one site. All participants (up to 20) are eligible for\n“Certificates of Attendance,” and accreditation, provided that accreditation\nrequirements are met. For groups larger than 20 or for additional sites, please\ncall +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"header-block-grey\"\u003eAccreditation Information\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eBarnett International is accredited by the\nAccreditation Council for Pharmacy Education as a provider of continuing\npharmacy education.  Participants will\nreceive 2 hours (0.2 CEUs) of continuing education credit for full\nparticipation, including the completion of a pre-test, post-test, and program\nevaluation.  Barnett International will\nissue a receipt of completion for earned CEUs within three weeks of program\ncompletion.  ACPE#: 0778-0000-17-080-L01-P.\nReleased: 3\/17. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp align=\"center\"\u003e\u003cspan class=\"bold\"\u003e\u003cspan\u003eHold\nthis course at your company! For more information, contact Naila Ganatra at +1\n215.413.2471. \u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp align=\"left\" class=\"Abstract\"\u003e \u003c\/p\u003e","products":[],"url":"https:\/\/www.barnettinternational.com\/collections\/cgmp-for-the-quality-control-laboratory.oembed","provider":"Barnett International ","version":"1.0","type":"link"}