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Title:MODEL IMPLEMENTACIJE DIREKTIV ZA IT V ŽIVLJENJSKEM CIKLU PROGRAMSKE OPREME
Authors:ID Kovač, Sergej (Author)
ID Leskovar, Robert (Mentor) More about this mentor... New window
Files:.pdf MAG_Kovac_Sergej_2010.pdf (1,32 MB)
MD5: 5A38FB53A0637DF7D4CC17CFDCD9B39A
PID: 20.500.12556/dkum/8ab08944-e558-481b-9cf7-9c045d078665
 
Language:Slovenian
Work type:Master's thesis
Organization:FOV - Faculty of Organizational Sciences in Kranj
Abstract:Magistrsko delo obravnava vpliv direktiv za IT v življenjskem ciklu programske opreme. Kratko so predstavljeni modeli razvoja programske opreme. Podan je pregled direktiv regulatornih organov FDA in EMA, standarda ISO12207 in priporočil GAMP na področju farmacevtske industrije in njihov vpliv na življenjski cikel informacijskega sistema. Direktive FDA so najstrožje direktive, ki predpisujejo delovanje posameznih informacijskih sistemov v farmacevtskem okolju. EMA je evropski regulatorni organ, ki v večini povzema direktive FDA prilagojene evropskemu tržišču.Predstavljen je nabor konceptov in praks za razvoj in podporo IT operacij ITIL. Za konkretno podjetje je izdelana primerjava klasifikacij informacijskih sistemov po direktivah in klasifikacija po korporacijskih pravilih. Ta primerjava omogoča enostavnejše sledenje zahtevam regulatornih organov, ki so povezane z razvojem in vzdrževanjem informacijskih sistemov. Podani predlogi za izboljšave trenutno vpeljanega življenjskega cikla informacijskega sistema so neposredno povezani z izpolnjevanjem zahtev obravnavanih direktiv za IT v farmacevtski industriji.
Keywords:Življenjski cikel razvoja programske opreme, Regulatorni organ, FDA, EMA, Upravljanje kakovosti, Validacija IS
Place of publishing:Maribor
Year of publishing:2010
PID:20.500.12556/DKUM-15349 New window
COBISS.SI-ID:6754835 New window
NUK URN:URN:SI:UM:DK:CBQMQKCB
Publication date in DKUM:30.11.2010
Views:2827
Downloads:362
Metadata:XML DC-XML DC-RDF
Categories:FOV
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Secondary language

Language:English
Title:IT DIRECTIVES IMPLEMENTATION MODEL IN THE SOFTWARE LIFE-CYCLE
Abstract:My Master’s Thesis evaluates the influence of IT directives in software development life cycle. The software development models are presented in brief. Furthermore, an overview of the FDA and EMA regulatory bodies’ directives, ISO12207 standard and GAMP recommendations for the field of pharmaceutical industry and their influence on the information system life cycle is presented. FDA directives are the strictest directives which regulate the functioning of individual information systems in the pharmaceutical environment. EMA is a European regulatory body, which mainly undertakes FDA’s directives adapted to the European market. A range of concepts and practises for the development and support of IT operations ITIL is presented. A comparison of the information system classification according to directives and the classification according to corporate rules has been made for an actual company. This comparison enables an easier following of the regulatory body demands, which are related to the development and maintenance of information systems. The given suggestions for improving the currently established information system life cycle are directly linked to the fulfilment of demands of the analysed IT directives in the pharmaceutical industry.
Keywords:System development lifecycle (SDLC), Regulatory body, FDA, EMA, Quality management in IT, IS validation


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