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.
Кључне речи:
medical product storage / activities and functions / conditions / management / skladištenje lekova / funkcije i aktivnosti / uslovi / upravljanje
Извор:
Procesna tehnika, 2002, 18, 2, 33-38
Издавач:
Savez mašinskih i elektrotehničkih inženjera i tehničara Srbije (SMEITS), Beograd
TY - 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 .
