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各位蒲友:
有纠正措施(CA)就必须或一定有预防措施嘛??在什么情况下只有纠正措施,而没有预防措施????
The acronym “CAPA” will not be used in this document because the concept of corrective action and preventive action has been incorrectly interpreted to assume that a preventive action is re-quired for every corrective action.
——————选自< Quality management system –Medical Devices – Guidance on corrective action and preventive action and related QMS processes>
"I remember the first time I read the GHTF document," recalls Valerie Welter, senior director of quality management for Teva Animal Health (St. Joseph, MO), a subsidiary of Teva USA, "and it was like a light at the end of a dark tunnel. For years, I, like many quality professionals, struggled with defining a preventive action as a requirement to close every CAPA. Procedures were based on defining a single definitive root cause, at least one corrective action and at least one preventive action. The GHTF document provides a logical escalation process associated with the evaluation, investigation, verification, implementation and effectiveness determinations associated with negative quality events as defined in the measurement, analysis, and improvement sections of the device QMS regulation."
补充内容 (2016-6-14 10:34):
偏差就必须调查或或者调查根本原因嘛????偏差就必须执行着CAPA嘛?????
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