<Record><identifier xmlns="http://purl.org/dc/elements/1.1/">URN:NBN:SI:doc-AQ6A9UT9</identifier><date>2022</date><creator>Vrbovšek, Lidija</creator><relation>documents/doc/A/URN_NBN_SI_doc-AQ6A9UT9_001.pdf</relation><relation>documents/doc/A/URN_NBN_SI_doc-AQ6A9UT9_001.txt</relation><format format_type="issue">4</format><format format_type="volume">73</format><format format_type="type">article</format><format format_type="extent">str. 313-320</format><identifier identifier_type="COBISSID_HOST">141356547</identifier><identifier identifier_type="ISSN">2536-4316</identifier><identifier identifier_type="URN">URN:NBN:SI:doc-AQ6A9UT9</identifier><language>slv</language><publisher publisher_location="Ljubljana">Slovensko farmacevtsko društvo</publisher><source>Farmacevtski vestnik</source><rights>InC</rights><subject language_type_id="eng">extemporaneously prepared medicines</subject><subject language_type_id="slv">magistralno zdravilo</subject><subject language_type_id="slv">obvladovanje tveganj</subject><subject language_type_id="slv">ocena tveganja</subject><subject language_type_id="slv">Resolucija CM/ResAP(2016)1</subject><subject language_type_id="eng">Resolution CM/ResAP(2016)1</subject><subject language_type_id="eng">risk assessment</subject><subject language_type_id="eng">risk management</subject><title>Ocena tveganja za magistralna zdravila</title><title>Risk assessment for extemporaneously prepared medicines</title></Record>