Zobrazeno 1 - 2
of 2
pro vyhledávání: '"bioequivalence of drug"'
Autor:
Škarijot, Jelena
Cilj istraživanja Cilj ovog specijalističkog rada je pregledno opisati regulatorne smjernice Europske agencije za lijekove (EMA) za ispitivanje bioraspoloživosti i provjere bioekvivalencije u postupku davanja odobrenja za stavljanje generičkog of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3671::6e6f456f14b8f2aab6231a7798bbe9d2
https://repozitorij.pharma.unizg.hr/islandora/object/pharma:1078
https://repozitorij.pharma.unizg.hr/islandora/object/pharma:1078
Publikováno v:
Expert review of pharmacoeconomicsoutcomes research. 14(2)
The Japanese pharmaceutical market, the world’s second largest, is traditionally renowned for the domination of patented drugs and the weakest generics share among major established economies. An in-depth observation of published evidence in Japane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0801f13aa797266e749b162f3dffdb0e
https://pubmed.ncbi.nlm.nih.gov/24450984
https://pubmed.ncbi.nlm.nih.gov/24450984
