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Zasnova informacijskega sistema po GMP standardih na področju farmacije
ID LEMUT, BLAŽ (Author), ID Zrnec, Aljaž (Mentor) More about this mentor... This link opens in a new window

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MD5: 1A9BC319D6CC2965D79783B3941A3A7D
PID: 20.500.12556/rul/ca016717-f196-4be1-93b0-f4fb5b575711

Abstract
Informacijska tehnologija ima iz dneva v dan vedno večji pomen v vseh vidikih našega življenja. V zadnjih dvajsetih letih smo priča silovitemu porastu uporabe informacijske tehnologije v farmaciji, kar je privedlo do potrebe po nadzoru njenega vpliva. Uradne agencije po svetu, ki so zadolžene za zdravje ljudi in živali, so določile, da za obratovanje v farmacevtski industriji morajo organizacije in podjetja slediti določenim standardom za zagotavljanje dobre proizvodne prakse. V okviru diplomskega dela se naprej osredotočimo na vpliv informacijske tehnologije v farmaciji, nato povzamemo GMP standarde ter predstavimo vpeljavo novega informacijskega sistema v farmacevtskem laboratoriju po priznanih navodil za zagotavljanje ustreznosti z GMP.

Language:Slovenian
Keywords:informacijski sistem, dobra proizvodna praksa, standardi, farmacija, smernice
Work type:Bachelor thesis/paper
Organization:FRI - Faculty of Computer and Information Science
Year:2017
PID:20.500.12556/RUL-91018 This link opens in a new window
Publication date in RUL:09.03.2017
Views:1919
Downloads:377
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Secondary language

Language:English
Title:Design of an information system following GMP standards in the pharmaceutical industry
Abstract:
Every day, the meaning of information technology increases in all aspects of our daily lives. Due to the fact that in the past twenty years we have witnessed a tremendous increase of information technology being used in the pharmaceutical industry, there is a need to regulate and control it. Agencies around the world which are responsible for protecting animal and public health established that organizations and companies need to follow good manufacturing practices in order to normally operate in the pharmaceutical industry. In the scope of the diploma thesis we first concentrate on the impact of information technology in the pharmaceutical industry, which we then follow up with a summary of the GMP practices and a detailed description of the implementation of a new information system in a pharmaceutical laboratory following generally accepted guidelines.

Keywords:information system, good manufacturing practices, standards, pharmaceutical industry, guidelines

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