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Kolonić, Teo; Bencetić Marijanović, Martina; Tomić, Siniša
Kemija u industriji, 06/2021, Volume: 70, Issue: 7-8Journal Article, Paper
Dobra proizvođačka praksa (GMP) je skup različitih smjernica, pravila i normi koje jamče učinkovitost, kvalitetu, sigurnost i dosljednost u proizvodnji i kontroli lijekova. Nadzor nad dobrom proizvođačkom praksom u Hrvatskoj provodi Agencija za lijekove i medicinske proizvode (HALMED). U svrhu održavanja konzistentnih inspekcijskih standarda, HALMED ima razvijen Poslovnik kakvoće izrađen u skladu s europskim smjernicama. Inspektori Agencije imaju odgovarajuća znanja i iskustvo te se trajno usavršavaju. Po obavljenoj inspekciji, HALMED izdaje proizvodnu dozvolu i potvrdu o provođenje dobre proizvođačke prakse (GMP potvrdu) za proizvođače u Republici Hrvatskoj te GMP potvrdu za proizvođače iz trećih zemalja. S obzirom na nemogućnost izlaska inspektora na teren uslijed pandemijske situacije, sve se češće pribjegava ocjeni na daljinu. Good Manufacturing Practice (GMP) is a set of different guidelines, rules and standards that guarantee effectiveness, quality, safety and consistency in manufacturing and quality control of medicinal products. To maintain consistency in inspection standards, HALMED has in place a Quality Manual developed according to European guidelines. The Agency inspectors are trained and experienced accordingly, and are permanently educated. After an inspection has been completed, HALMED issues a manufacturing license and a GMP certificate for manufacturers located in the Republic of Croatia or a GMP certificate for manufacturers from third countries. Due to the pandemic situation that prevents inspectors to travel to manufacturing sites abroad, they proceed with the distant assessment of manufacturers.
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