{"product_id":"9781032917511-pharmaceutical-computer-systems-validat","title":"Pharmaceutical Computer Systems Validation","description":"\u003cmeta content=\"text\/html; charset=utf-8\" http-equiv=\"Content-Type\"\u003e\u003cp\u003e\u003cspan\u003eQuality Assurance, Risk Management and Regulatory Compliance\u003cbr\u003eThoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and verification principles and how to put them into practice. To provide the current best practice and guidance on identifying and implementing improvements for computer systems, the text extensively review\u003cbr\u003e\u003cp\u003eThoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and verification principles and how to put them into practice. To provide the current best practice and guidance on identifying and implementing improvements for computer systems, the text extensively reviews regulations of pharmaceuticals, healthcare products, blood processing, medical devices, clinical systems, and biotechnology. Ensuring that organizations transition smoothly to the new system, this guide explains how to implement the new GMP paradigm while maintaining continuity with current practices. In addition, all 24 case studies from the previous edition have been revised to reflect the new system.\u003c\/p\u003e\n\u003cp\u003eKey topics in Pharmaceutical Computer Systems Validation, Second Edition include:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eGAMP5, ASTM 2500, EU GMP (Annex 11), and US GMP revisions to regulatory requirements for electronic records and signatures that should be published in 2008\u003c\/li\u003e\n\u003cli\u003eICH Guidance Q8, Q9, and Q10 expectations\u003c\/li\u003e\n\u003cli\u003eFDA cGMPs for the 21st Century Initiative and associated guidance\u003c\/li\u003e\n\u003cli\u003ePIC\/S Guidance on Good Practice for Computerized Systems in GxP Environments\u003c\/li\u003e\n\u003cli\u003eWK9864 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment\u003c\/li\u003e\n\u003cli\u003ethe indirect developments from FDA\/EU\/Japan regulators and industry\u003c\/li\u003e\n\u003cli\u003ethe role of QA department, and internal and external suppliers\u003c\/li\u003e\n\u003cli\u003ethe integration of computer systems validation into single overall approach for wider system\u003c\/li\u003e\n\u003cli\u003epractical guidance on handling common high, medium, and low risk issues that can occur during the life cycle of a computer system\u003c\/li\u003e\n\u003cli\u003emanaging outsource partners and handling legacy systems\u003c\/li\u003e\n\u003cli\u003etopical issues uncovered by regulatory authorities including US FDA\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cbr\u003e\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e","brand":"Rarewaves","offers":[{"title":"Default Title","offer_id":55447225139574,"sku":"9781032917511","price":64.9,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0092\/7504\/8033\/files\/orig_36642171.jpg?v=1760671036","url":"https:\/\/www.rarewaves.com\/products\/9781032917511-pharmaceutical-computer-systems-validat","provider":"Rarewaves.com","version":"1.0","type":"link"}