Specific processes and requirements in the management of medical products storage
Specifični procesi i zahtevi upravljanja skladištem lekova
Abstract
The knowledge of raw materials, active and final drug forms are included in the requirements for processing and management of medical product storage. In this paper, the basic guidelines for the final draft of FIP-WHO Good Storage Practice are presented. The main requirements for quality assurance of medical products are storage conditions and unification of container labeling, regarding the stability test.
Specifični procesi i zahtevi upravljanja skladištem lekova podrazumevaju poznavanje osnovnih materijala za proizvodnju lekova i gotovih lekova, te pravilnog postupka skladištenja preporučenog u dokumentu FIP - WHO Good Storage Practice, čije su osnovne smernice iznesene u ovom radu. Uslovi skladištenja lekova i unifikacije označavanja kontejnera u vezi su sa testovima stabilnosti i od vitalnog su značaja za očuvanje kvaliteta leka.
Keywords:
medical product storage / activities and functions / conditions / management / skladištenje lekova / funkcije i aktivnosti / uslovi / upravljanjeSource:
Procesna tehnika, 2002, 18, 2, 33-38Publisher:
- Savez mašinskih i elektrotehničkih inženjera i tehničara Srbije (SMEITS), Beograd
Collections
Institution/Community
PharmacyTY - JOUR AU - Tasić, Ljiljana AU - Ćuprić, Nenad PY - 2002 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/370 AB - The knowledge of raw materials, active and final drug forms are included in the requirements for processing and management of medical product storage. In this paper, the basic guidelines for the final draft of FIP-WHO Good Storage Practice are presented. The main requirements for quality assurance of medical products are storage conditions and unification of container labeling, regarding the stability test. AB - Specifični procesi i zahtevi upravljanja skladištem lekova podrazumevaju poznavanje osnovnih materijala za proizvodnju lekova i gotovih lekova, te pravilnog postupka skladištenja preporučenog u dokumentu FIP - WHO Good Storage Practice, čije su osnovne smernice iznesene u ovom radu. Uslovi skladištenja lekova i unifikacije označavanja kontejnera u vezi su sa testovima stabilnosti i od vitalnog su značaja za očuvanje kvaliteta leka. PB - Savez mašinskih i elektrotehničkih inženjera i tehničara Srbije (SMEITS), Beograd T2 - Procesna tehnika T1 - Specific processes and requirements in the management of medical products storage T1 - Specifični procesi i zahtevi upravljanja skladištem lekova VL - 18 IS - 2 SP - 33 EP - 38 UR - https://hdl.handle.net/21.15107/rcub_farfar_370 ER -
@article{ author = "Tasić, Ljiljana and Ćuprić, Nenad", year = "2002", abstract = "The knowledge of raw materials, active and final drug forms are included in the requirements for processing and management of medical product storage. In this paper, the basic guidelines for the final draft of FIP-WHO Good Storage Practice are presented. The main requirements for quality assurance of medical products are storage conditions and unification of container labeling, regarding the stability test., Specifični procesi i zahtevi upravljanja skladištem lekova podrazumevaju poznavanje osnovnih materijala za proizvodnju lekova i gotovih lekova, te pravilnog postupka skladištenja preporučenog u dokumentu FIP - WHO Good Storage Practice, čije su osnovne smernice iznesene u ovom radu. Uslovi skladištenja lekova i unifikacije označavanja kontejnera u vezi su sa testovima stabilnosti i od vitalnog su značaja za očuvanje kvaliteta leka.", publisher = "Savez mašinskih i elektrotehničkih inženjera i tehničara Srbije (SMEITS), Beograd", journal = "Procesna tehnika", title = "Specific processes and requirements in the management of medical products storage, Specifični procesi i zahtevi upravljanja skladištem lekova", volume = "18", number = "2", pages = "33-38", url = "https://hdl.handle.net/21.15107/rcub_farfar_370" }
Tasić, L.,& Ćuprić, N.. (2002). Specific processes and requirements in the management of medical products storage. in Procesna tehnika Savez mašinskih i elektrotehničkih inženjera i tehničara Srbije (SMEITS), Beograd., 18(2), 33-38. https://hdl.handle.net/21.15107/rcub_farfar_370
Tasić L, Ćuprić N. Specific processes and requirements in the management of medical products storage. in Procesna tehnika. 2002;18(2):33-38. https://hdl.handle.net/21.15107/rcub_farfar_370 .
Tasić, Ljiljana, Ćuprić, Nenad, "Specific processes and requirements in the management of medical products storage" in Procesna tehnika, 18, no. 2 (2002):33-38, https://hdl.handle.net/21.15107/rcub_farfar_370 .