A risk-based process validation approach and establishment of a validation program for medical device manufacturers with an emphasis on equipment qualification

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:ProQuest Dissertations and Theses (2014)
मुख्य लेखक: Bilgin, Pelin
प्रकाशित:
ProQuest Dissertations & Theses
विषय:
ऑनलाइन पहुंच:Citation/Abstract
Full Text - PDF
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100 1 |a Bilgin, Pelin 
245 1 |a A risk-based process validation approach and establishment of a validation program for medical device manufacturers with an emphasis on equipment qualification 
260 |b ProQuest Dissertations & Theses  |c 2014 
513 |a Dissertation/Thesis 
520 3 |a The Food and Drug Administration's 2011 Process Validation Guidance for the medical device and pharmaceutical industry emphasizes utilizing a risk-based, decision-making procedure during process validation activities. Those guidelines, however, do not provide specific examples or a structured methodology to manufacturers for establishing a risk-based validation program. The focus of this project has been developed as part of a continuous quality improvement effort by the ABC medical device manufacturing company. This project evaluates current process validation requirements and guidelines for medical device manufacturers and outlines a step-by-step approach for a risk-based process validation program with an emphasis on equipment qualifications. Supporting documents such as validation plans, equipment qualification templates, and risk matrices are included. The goal is to help other medical device manufacturers implement a compliant process validation program 
653 |a Engineering 
653 |a Pharmaceutical sciences 
773 0 |t ProQuest Dissertations and Theses  |g (2014) 
786 0 |d ProQuest  |t ProQuest Dissertations & Theses Global 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/1669485407/abstract/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch 
856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/1669485407/fulltextPDF/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch