GMP Training Courses - APIs and Excipients

Impurities Forum- Part I:  General Strategies

Copenhagen, Denmark

27 June 2017

Impurities Forum- Part I: General Strategies

Impurities Forum- Part II:  Elemental Impurities

Copenhagen, Denmark

28 June 2017

Impurities Forum- Part II: Elemental Impurities

Impurities Forum Post-Conference Workshop - The Elemental Impurities Database for excipients

Copenhagen, Denmark

29 June 2017

Impurities Forum Post-Conference Workshop - The Elemental Impurities Database for excipients

Impurities Forum- Part I and Part II

Copenhagen, Denmark

27-28 June 2017

Impurities Forum- Part I and Part II

Quality by Design in API Manufacturing

Heidelberg, Germany

11-12 October 2017

Quality by Design in API Manufacturing

QbD in Drug Product Devbelopment AND QbD in API Manufacturing

Heidelberg, Germany

10-12 October 2017

QbD in Drug Product Devbelopment AND QbD in API Manufacturing

Elemental Impurities and CEPs – Requirements for new
CEP applications, already existing CEPs and CEP revisions<br>Pre-conference session to the 20th APIC/CEFIC European Conference

Berlin, Germany

24 October 2017

Elemental Impurities and CEPs – Requirements for new CEP applications, already existing CEPs and CEP revisions Pre-conference session to the 20th APIC/CEFIC European Conference

20th APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (GMP Part)

Berlin, Germany

25-26 October 2017

20th APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (GMP Part)

20th APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (RA Part)

Berlin, Germany

26-27 October 2017

20th APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (RA Part)

20th APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (All 3 Conference Days)

Berlin, Germany

25-27 October 2017

20th APIC/CEFIC European Conference on Active Pharmaceutical Ingredients (All 3 Conference Days)

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

Barcelona, Spain

23-24 November 2017

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

ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis

Vienna, Austria

4-6 December 2017

ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis

GMP Conferences by Topics

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