Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Oleksandr Gryzodub"'
Publikováno v:
SSP Modern Law and Practice. 3:1-23
The multidisciplinary context of the State Pharmacopoeia of Ukraine in drug quality systems was justified through an interdisciplinary study of pharmaceutical business organization, quality control, standardization, drug technology, management, marke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba600dc41c686d4246b24f0db265a9b2
https://doi.org/10.53933/sspmlp.v3i1.81
https://doi.org/10.53933/sspmlp.v3i1.81
Autor:
Oleksandr Gryzodub
Publikováno v:
SSP Modern Law and Practice. 2:1-21
Provision to every citizen, patient, and person in the system of legal relationship "doctor-patient-pharmacist" the right to life, health, and safety during the circulation of vital medicinal products of all clinical and pharmacological, nomenclature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d32cbb8a1bd170ceb72e6f454a833893
https://doi.org/10.53933/sspmlp.v2i3.67
https://doi.org/10.53933/sspmlp.v2i3.67
Publikováno v:
ScienceRise: Pharmaceutical Science, Iss 6 (28), Pp 56-67 (2020)
Aim . The paper intends to frame and pilot the optimised science-based principles of the assay transfer. Materials and methods . The research was performed on desloratadine film-coated tablets, using an analytical balance Mettler Toledo XP 205DR and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::828ff980aeba10fd29abb405037ecf22
http://journals.uran.ua/sr_pharm/article/view/221721
http://journals.uran.ua/sr_pharm/article/view/221721
Publikováno v:
EUREKA: Health Sciences, Iss 6, Pp 74-87 (2020)
Aim. This work aimed to validate an assay procedure for desloratadine tablets by direct spectrophotometric method. Materials and methods. A pilot-scale batch of the pharmaceutical preparationAlerdez, film-coated tablets containing 5 mg of desloratadi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5037df82df937d83504d7300e2acf77b
https://doi.org/10.21303/2504-5679.2020.001527
https://doi.org/10.21303/2504-5679.2020.001527
Publikováno v:
ScienceRise: Pharmaceutical Science, Vol 0, Iss 3 (19), Pp 4-10 (2019)
Aim.The increase in the pharmaceutical market of Ukraine of the range of medicines leads to stricter requirements for their quality. According to the requirements of international standards ISO, ICH, GMP, current legislation of Ukraine and the State
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400dd61e124569b9e212e5032c670b5b
http://journals.uran.ua/sr_pharm/article/view/172046
http://journals.uran.ua/sr_pharm/article/view/172046