497 KB0 KB200720252025Cerovšek, MitjaPeklaj, Kristianštevilka:1letnik:31str. 26-32ISSN:1318-7279COBISSID_HOST:228730115URN:URN:NBN:SI:doc-YOIMSOQ4enUniverza v Ljubljani, Fakulteta za strojništvoVentil (Ljubljana)compliancecomputerized systemsdata integrityGAMP 5pharmacyregulationsvalidationImplementing laboratory computerized systems in pharmaceutical industry| regulatory compliance|The implementation of computerized systems in pharmaceutical industry must meet the compliance with regulatory requirements, assure high level of data integrity (DI) and product quality. This study reviews European legislation, the European and U.S. pharmacopoeias, and global guidelines, such as GAMP 5 and ALCOA++, to identify the necessary standards and best practices. Key directives of European and U.S legalisation emphasize the importance of system validation, quality risk management and secure data handling. The study highlights validation processes categorized by system complexity according to GAMP 5. Additionally, guidelines like ALCOA++ provide a robust framework for achieving DI throughout the data lifecycle. By adhering to these requirements, pharmaceutical manufacturers can ensure regulatory compliance, maintain high-quality standards and safeguard patient safetyTEXTznanstveno časopisjejournalsSlovenian National E-content AggregatorNational and University Library of SloveniaUniverza v Ljubljani, Fakulteta za strojništvo