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13
November
2023
09:00
ONLINE seminari
13.11.2023. - Glavni spis o farmakovigilanciji (PSMF) - izrada i održavanje
14
November
2023
09:00
ONLINE seminari
14.11. - 15.11.2023. - Farmaceutska regulativa, uloge i odgovornosti odgovorne osobe za puštanje serije lijeka u promet
16
November
2023
09:00
ONLINE seminari
16.11. - 17.11.2023. - Upravljanje rizicima za medicinske proizvode prema normi ISO 14971:2019/A11:2021 i smjernici ISO/TR 24971:2020
20
November
2023
09:00
ONLINE seminari
20.11.2023. - Mikrobiologija u proizvodnji lijekova za nemikrobiologe
21
November
2023
09:00
ONLINE seminari
21.11.2023. - In vitro dijagnostika - zahtjevi Uredbe (EU) 2017/746 za distributere i uvoznike
22
November
2023
09:00
ONLINE seminari
22.11.2023. - Integritet podataka u GMP/GDP okruženju
28
November
2023
09:00
ONLINE seminari
28.11. - 30.11.2023. - Medicinski proizvodi - zahtjevi Uredbe (EU) 2017/745- dobra proizvođačka praksa, razvrstavanje, registracija i označavanje CE oznakom
30
November
2023
09:00
ONLINE seminari
30.11.2023. - Kvalifikacija vozila i verifikacija transportnih ruta za lijekove i medicinske proizvode
01
December
2023
09:00
ONLINE seminari
01.12.2023. - Kako napisati standardni operativni postupak (SOP) i radnu uputu - radionica
05
December
2023
09:00
ONLINE seminari
05.12.2023. - Istraga korijenskog uzroka nesukladnosti, korekcije i korektivne radnje za distributere lijekova - radionice
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