Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q359176> ?p ?o }
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- Q359176 subject Q13252734.
- Q359176 subject Q6933255.
- Q359176 subject Q7056690.
- Q359176 subject Q7273604.
- Q359176 subject Q8894882.
- Q359176 abstract "Validation is a process of establishing documentary evidence demonstrating that a procedure, process, or activity carried out in production or testing maintains the desired level of compliance at all stages. In Pharma Industry it is very important apart from final testing and compliance of product with standard that the process adapted to produce itself must assure that process will consistently produce the expected results. Here the desired results are established in terms of specifications for out come of the process. Qualification of systems and equipment is therefore a part of process of validation. It is a requirement of food and drug, pharmaceutical regulating agencies like FDA's good manufacturing practices guidelines. Since a wide variety of procedures, processes, and activities need to be validated, the field of validation is divided into a number of subsections including the following:Equipment validationFacilities validationHVAC system validationCleaning validationProcess ValidationAnalytical method validationComputer system validationPackaging validationCold chain validationSimilarly, the activity of qualifying systems and equipment is divided into a number of subsections including the following:Design qualification (DQ)Component qualification (CQ)Installation qualification (IQ)Operational qualification (OQ)Performance qualification (PQ)↑".
- Q359176 wikiPageExternalLink Instrumentation1_Swartz_rv.pdf.
- Q359176 wikiPageExternalLink about-21-cfr-part-11-electronic-records-electronic-signatures.
- Q359176 wikiPageExternalLink ucm124720.html.
- Q359176 wikiPageExternalLink index-eng.php.
- Q359176 wikiPageExternalLink www.pharmacistspharmajournal.org.
- Q359176 wikiPageExternalLink validation.htm.
- Q359176 wikiPageWikiLink Q12140.
- Q359176 wikiPageWikiLink Q1292017.
- Q359176 wikiPageWikiLink Q13252734.
- Q359176 wikiPageWikiLink Q1500490.
- Q359176 wikiPageWikiLink Q15708570.
- Q359176 wikiPageWikiLink Q1755993.
- Q359176 wikiPageWikiLink Q18344773.
- Q359176 wikiPageWikiLink Q188522.
- Q359176 wikiPageWikiLink Q1916302.
- Q359176 wikiPageWikiLink Q204711.
- Q359176 wikiPageWikiLink Q207822.
- Q359176 wikiPageWikiLink Q254125.
- Q359176 wikiPageWikiLink Q2919644.
- Q359176 wikiPageWikiLink Q5130576.
- Q359176 wikiPageWikiLink Q5271952.
- Q359176 wikiPageWikiLink Q573538.
- Q359176 wikiPageWikiLink Q592197.
- Q359176 wikiPageWikiLink Q621636.
- Q359176 wikiPageWikiLink Q621977.
- Q359176 wikiPageWikiLink Q6554101.
- Q359176 wikiPageWikiLink Q6933255.
- Q359176 wikiPageWikiLink Q7056690.
- Q359176 wikiPageWikiLink Q7180730.
- Q359176 wikiPageWikiLink Q7273604.
- Q359176 wikiPageWikiLink Q7418324.
- Q359176 wikiPageWikiLink Q7911675.
- Q359176 wikiPageWikiLink Q7921330.
- Q359176 wikiPageWikiLink Q8894882.
- Q359176 comment "Validation is a process of establishing documentary evidence demonstrating that a procedure, process, or activity carried out in production or testing maintains the desired level of compliance at all stages. In Pharma Industry it is very important apart from final testing and compliance of product with standard that the process adapted to produce itself must assure that process will consistently produce the expected results.".
- Q359176 label "Validation (drug manufacture)".