GMP Training Courses - APIs and Excipients

Name: Drug Master File Procedures in the EU, the US and Japan
Start: 2019-09-17
End: 2019-09-17
Location: Drug Master File Procedures in the EU, the US and Japan

Copenhagen, Denmark

17/18 September 2019

Drug Master File Procedures in the EU, the US and Japan

Webinar: EMA´s Q & A regarding PDE-values

Heidelberg, Germany

Thursday, 17 October 2019 14.00 - 15.30 h

Webinar: EMA´s Q & A regarding PDE-values

How to audit registered Starting Materials Manufacturers<br>Pre-conference session to the 22nd APIC/CEFIC European Conference

Prague, Czech Republic

22 October 2019

How to audit registered Starting Materials Manufacturers Pre-conference session to the 22nd APIC/CEFIC European Conference

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (GMP Part)

Prague, Czech Republic

23-24 October 2019

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (GMP Part)

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (RA Part)

Prague, Czech Republic

24-25 October 2019

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (RA Part)

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (All 3 Conference Days)

Prague, Czech Republic

23-25 October 2019

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (All 3 Conference Days)

GMP for Cannabis – what you need to know

Heidelberg, Germany

29/30 October 2019

GMP for Cannabis – what you need to know

ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis

Praha, Czech Republic

4-6 November 2019

ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis

ICH Q7 Compliance for APIs Manufactured by Cell Culture/Fermentation

Praha, Czech Republic

4-6 November 2019

ICH Q7 Compliance for APIs Manufactured by Cell Culture/Fermentation

Handling of Foreign Particles in APIs and Excipients

Praha, Czech Republic

5/6 November 2019

Handling of Foreign Particles in APIs and Excipients

Praha, Czech Republic

6-8 November 2019

ICH Q7 Auditor Training Course

Global registration and Life Cycle Management for APIs

Vienna, Austria

10-12 March 2020

Global registration and Life Cycle Management for APIs

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GMP Training Courses - APIs and Excipients

Drug Master File Procedures in the EU, the US and Japan

Webinar: EMA´s Q & A regarding PDE-values

How to audit registered Starting Materials Manufacturers Pre-conference session to the 22nd APIC/CEFIC European Conference

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (GMP Part)

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (RA Part)

22nd APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (All 3 Conference Days)

GMP for Cannabis – what you need to know

ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis

ICH Q7 Compliance for APIs Manufactured by Cell Culture/Fermentation

Handling of Foreign Particles in APIs and Excipients

ICH Q7 Auditor Training Course

Global registration and Life Cycle Management for APIs

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