PDA Italy Chapter Webinar - Annex 1: How To Interpret the Draft for the Second Consultation
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English Translation:
Annex 1: How to interpret the draft for the second consultation
Since 1946, our mission has been to disseminate technical know-how in the pharmaceutical sector.
Take part in the next PDA Italy Chapter event and take part in the second webinar organized for Thursday 30 April from 10:00 am to 11:00 am
Topic - "Annex 1: How to interpret the draft for the second consultation"
In this introductory webinar to the planned series on the review topic of Annex 1, the key points to start will be taken into consideration to consider with reference to the most significant changes of the document GMP from 2008 to today:
- The structure of the document proposed for the second consultation, starting from the comment phases and the correction process by the Working Group (WG): PIC / s, EC, WHO.
- Points that are still open to comments from associations
- Which sessions will no longer be reviewed?
Also, for this second webinar the registration is free.
Select “Register now” to save your seat!
SAVE THE DATE!
To complete the webinar of 30 April, 3 further in-depth appointments will follow, divided into the following topics:
- 6 MAY 2020, from 10:00 am to 11:00 am
Topic: The overview and qualification requirements in the different types of production processes - 13 MAY 2020, from 10:00 am to 11:00 am
Topic: The requirements and challenges required by the new chapter on environmental monitoring the new quality levels established - 20 MAY 2020, from 10:00 am to 11:00 am
Topic: The characterization and changes related to the professional figure in pharmaceutical production
Follow us in the next appointments on Annex 1 and other important issues related to pharmaceutical production. We hope many of you will come!
See you soon,
Angela Molaschi
Dal 1946, la nostra missione è disseminare know how tecnico nel settore farmaceutico.
Prendi parte al prossimo appuntamento di PDA Italy Chapter e partecipa al secondo webinar organizzato per giovedì 30 Aprile dalle 10.00 alle 11.00:
“Annex 1: come interpretare il draft per la seconda consultazione”
In questo webinar introduttivo alla serie prevista sull’argomento revisione dell’ Annex 1, verranno presi in considerazione i punti chiave da cominciare a considerare in riferimento ai cambiamenti più significativi del documento GMP dal 2008 ad oggi:
- la struttura del documento proposto per la seconda consultazione, a partire dalle fasi di commenti e l’iter di correzione da parte del Working Group (WG): PIC/s, EC, WHO.
- I punti che sono ancora aperti ai commenti da parte delle associazioni
- Quali le sessioni che non saranno più oggetto di revisione?
Anche per questo secondo webinar l'iscrizione è gratuita. Registrati subito cliccando qui.
SAVE THE DATE!
A completamento del webinar del 30 Aprile, seguiranno 3 ulteriori appuntamenti di approfondimento, suddivisi nelle seguenti tematiche:
- 6 MAGGIO 2020, dalle 10.00 alle 11.00
La panoramica e requisiti di qualifica nelle diverse tipologie dei processi produttivi - 13 MAGGIO 2020, dalle 10.00 alle 11.00
I requisiti e le sfide richieste dal nuovo capitolo sul monitoraggio ambientale
I nuovi livelli qualitativi stabiliti - 20 MAGGIO 2020, dalle 10.00 alle 11.00
La caratterizzazione e i cambiamenti relativi alla figura professionale nelle produzioni farmaceutiche
Per maggiori informazioni sui contenuti e le modalità di iscrizione clicca qui
Seguiteci nei prossimi appuntamenti su Annex 1 e altre importanti tematiche legate alla produzione farmaceutica. Vi aspettiamo numerosi!
A presto,
Angela Molaschi
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Milano, IT
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