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and corrective action system
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171	Responsible Office/Division Title: MDSAP QMS Control of Quality Records Procedure Document No.: MDSAP QMS P0007.001 Add to Reading List Source URL: www.fda.gov Language: English Information technology management Quality Management Content management systems Administration Quality management system Records management Document management system Corrective and preventive action Quality management Business Technology
172	Responsible Office/Division Title: MDSAP QMS Preventive Action (PA) Procedure Document No.: MDSAP QMS P0010.001 Add to Reading List Source URL: www.fda.gov Language: English Business Form Corrective and preventive action Pharmaceutical industry Preventive action Quality management system ISO Nonconformity Quality management Quality Management
173	Responsible Office/Division Title: MDSAP QMS Internal Assessment Procedure Document No.: MDSAP QMS P0008.002 Add to Reading List Source URL: www.fda.gov Language: English Management Technology Corrective and preventive action Pharmaceutical industry ISO Quality management system Quality management Quality Business
174	Microsoft Word - MDSAP QMS F0005 1 Management Review Report Form.doc Add to Reading List Source URL: www.fda.gov Language: English Management Evaluation Auditing Corrective and preventive action Pharmaceutical industry Quality management system Management review Preventive action Audit Quality management Quality Business
175	Implementation Procedures Guide for Air Operators and Approved Maintenance Organizations (TP[removed]Appendix B - Gap Analysis Form Safety Management System Requirements Response (Yes/No) If yes, state where the requireme Add to Reading List Source URL: www.tc.gc.ca Language: English - Date: 2010-05-21 12:20:20 Disaster preparedness Emergency management Humanitarian aid Occupational safety and health Corrective and preventive action Internal audit Audit Sustainable Development Strategy in Canada Safety Management Systems Business Ethics Safety
176	Microsoft Word - MDSAP QMS F0008[removed]Assessment Checklist (3).doc Add to Reading List Source URL: www.fda.gov Language: English Evaluation Management Quality management system Auditing Corrective and preventive action ISO Preventive action Audit Internal audit Quality management Quality Business
177	Materials Laboratory Environmental Health and Safety Manual M 46-04 Add to Reading List Source URL: www.wsdot.wa.gov Language: English - Date: 2011-04-25 19:14:56 Evaluation Auditing Corrective and preventive action Pharmaceutical industry Internal audit Preventive action Right to know Management system Sustainable Development Strategy in Canada Quality Business Management
178	Microsoft Word - RDIMS-#[removed]v2-SI_SUR-006_ISSUE_2_-_SMS_-_CIVIL_AVIATION_NON-COMPLIANCE_EVEN_REVIEW_PROCESS.DOC Add to Reading List Source URL: tc.gc.ca Language: English - Date: 2010-06-22 12:54:00 Technology Quality Administrative law Air safety Aviation law Safety Management Systems Corrective and preventive action Audit Management system Safety Transport Security
179	Instructions for Tier 2 GWR Failure to Comply with Corrective Action Plan or Schedule Template Template Attached A system’s failure to take corrective action within the required timeframe or failure to be in complianc Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-25 22:15:07 Chemistry Corrective and preventive action Management Pharmaceutical industry Drinking water Water Business Matter Quality
180	Microsoft Word - EMPGB[removed]Final.doc Add to Reading List Source URL: www.doi.gov Language: English - Date: 2012-01-19 19:29:36 United States Department of Homeland Security Business Quality Corrective and preventive action Pharmaceutical industry HSEEP Incident management Management system Disaster preparedness Management Emergency management

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