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Process validation
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#	Item
521	BREAKOUT GROUP #4 B (Flip Chart[removed]What feed safety programs are operating today (industry and government) and can they be made available for review by the FDA? [for example, state Egg Safety Programs, trade associa Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-12-08 14:30:55 Food safety Pharmaceutical sciences Pet foods Hazard analysis Hazard analysis and critical control points Process management Validation Association of American Feed Control Officials Quality assurance Food and drink Food and Drug Administration Health
522	Technical Support Document: [removed]Models and Computer Codes Add to Reading List Source URL: epa.gov Language: English - Date: 2006-03-29 14:14:49 Procedural programming languages Cluster computing OpenVMS Validation Software development process Requirement Compaq DEC Alpha Configuration management Computing Technical communication Instruction set architectures
523	Concept of Technical Areas and Related Competencies Add to Reading List Source URL: cdm.unfccc.int Language: English - Date: 2011-04-05 11:03:54 Clinical research Quality Validation Clean Development Mechanism Construction Science Systems engineering process Verification and validation Evaluation Pharmaceutical industry Validity Systems engineering
524	ventis November 3,2003 Via fax and UPS Dockets Management Branch (HFA-305) Food and Drug Administration 5630 Fishers Lane, Room 1061 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-12-08 14:23:29 Management Evaluation Validity Design for X Process analytical technology Validation Quality assurance Specification Software development process Quality Pharmaceutical industry Science
525	PDF Document Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-11-12 17:50:23 Pharmacology Validation Process analytical technology Purdue Pharma Title 21 CFR Part 11 Food and Drug Administration Quality assurance Pharmaceutical industry Pharmaceutical sciences Pharmaceutics
526	ASSESSMENT REPORT 11‐03 FEDERAL DIGITAL SYSTEM (FDSYS) INDEPENDENT VERIFICATION AND VALIDATION – Add to Reading List Source URL: gpo.gov Language: English - Date: 2010-12-20 05:46:17 Software development process Transition methodology Code of Federal Regulations Management Science Business Federal Digital System Project management office United States Government Printing Office
527	Guidance for Industry PAT — A Framework for Innovative Pharmaceutical Manufacturing and Quality Assurance DRAFT GUIDANCE Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-12-05 09:20:34 Quality Clinical research Design for X Process analytical technology Quality by Design Food and Drug Administration Quality management system Center for Drug Evaluation and Research Validation Pharmaceutical sciences Pharmaceutical industry Pharmacology
528	[removed]INT_summary.indd Add to Reading List Source URL: gpo.gov Language: English - Date: 2009-10-28 11:16:45 Quality Validation Validity Systems engineering process Acceptance testing Requirement Technology Business Science Systems engineering Clinical research Pharmaceutical industry
529	AIan Goldhammer, PhD ASSOCIATE VICE PRESIDENT US REQULATORY AFFAIRS Dockets Management Branch Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English - Date: 2002-08-08 09:45:20 Science Validity Software development Quality Formal methods Validation Verification and validation Title 21 CFR Part 11 Software development process Pharmaceutical industry Software testing Technology
530	UID Staff Process Quick Reference Guide Begin at Step 1 to perform the UID Staff process Complete ALL 8 steps before Add to Reading List Source URL: www.ncpublicschools.org Language: English - Date: 2013-07-05 17:15:53 Computer icon Pictograms Filename extension Batch file Data validation Computing Data Information

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