MediaVision Schulungen (Themen)
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Ana-lytik |
GMP 1 |
GMP 2 |
GMP
für Wirkstoffe |
GMP + |
GMP R |
GMP Z |
GDP 1 |
GDP 2 |
GDP 3 |
GLP |
Mikro-leben |
| Abweichungen |
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+ |
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+ |
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| Abzeichnen |
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+ |
+ |
+ |
+ |
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| Analyse |
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+ |
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| Änderungskontrolle |
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| angelieferte Produkte |
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++ |
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++ |
+++ |
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| An- und Abmelden |
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| Audit trail |
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+ * |
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| Ausliefern |
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+ |
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| Beschädigung |
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+ |
+ |
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+ |
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| Betriebskleidung |
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++ |
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| Bilanzierung |
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+ |
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| Desinfektion |
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+ |
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| Dokumentation |
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+ |
+ |
+ |
+ |
+ |
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| Etikettierung |
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+ |
+ |
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+ |
+ |
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| FIFO/FEFO |
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+ |
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+ Thema ++ Hauptthema +++ zentrale Thema des Kurses + * nur in der Pharma Version
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Ana-lytik |
GMP 1 |
GMP 2 |
GMP
für Wirkstoffe |
GMP + |
GMP R |
GMP Z |
GDP 1 |
GDP 2 |
GDP 3 |
GLP |
Mikro-leben |
gefährliche Stoffe |
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+ |
+ |
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+ |
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Hygiene |
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Identifizierung |
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+ |
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+ |
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Inspektion |
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+ |
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+ |
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| Kalibrierung |
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+ |
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| Kalte Kette |
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+ |
+++ |
+ |
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Kommissionieren |
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++ |
++ |
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Kontrollen |
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+ |
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+ |
+ |
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| konzentriert Arbeiten |
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+ |
+ |
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| Krankheit |
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+ |
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| (Kreuz)Kontamination |
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+ |
+ |
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| Laboratorium |
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++ |
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+++ |
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| Lager |
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++ |
++ |
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Lagerung |
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+ |
++ |
+ |
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| Line-clearance |
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+ |
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| Logbuch |
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+ |
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+ |
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| Melden |
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+ |
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+ |
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| Mikroorganismen |
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+ |
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Monitorierung |
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+ |
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+ |
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+ Thema ++ Hauptthema +++ zentrale Thema des Kurses + * nur in der Pharma Version
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| |
Ana-lytik |
GMP 1 |
GMP 2 |
GMP
für Wirkstoffe |
GMP + |
GMP R |
GMP Z |
GDP 1 |
GDP 2 |
GDP 3 |
GLP |
Mikro-leben |
| Ordnung & Sauberkeit |
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+ |
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+ |
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| Probenahmen |
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+ |
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+ |
+ |
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| Prozeduren |
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+ |
+ |
+ |
+ |
+ |
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| QK/QS (Qual. Abteilung) |
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+ |
+ |
+ |
+ |
+ |
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| Qualifizierung |
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Quarantäne |
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Registrierung |
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+ |
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| Reinigung |
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+ |
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| Reinraum |
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++ |
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| Rückgabe/-ruf |
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++ |
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+ |
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| Schulung |
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+ |
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+ |
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Spezifikationen |
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Sterilisation |
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+ |
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| Transport |
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++ |
++ |
+ |
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| Validierung |
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+ |
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+ |
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Verwaltung |
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| Verwechslung |
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+ |
+ |
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Wartung |
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+ |
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Zeitdruck |
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+ |
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+ |
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+ Thema ++ Hauptthema +++ zentrale Thema des Kurses + * nur in der Pharma Version
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