GMP Training Courses - Vienna

Name: Computerised System Validation: Introduction to Risk Management + GAMP 5 Approach
Start: 2023-04-25
End: 2023-04-25
Location: Computerised System Validation: Introduction to Risk Management + GAMP 5 Approach

Vienna, Austria

25-28 April 2023

Computerised System Validation: Introduction to Risk Management + GAMP 5 Approach Learn How to Plan, Implement and Document Effectively Computer Validation Activities

Vienna, Austria

25 April 2023

Computerised System Validation: Introduction to Risk Management Book together with the course "Computerised System Validation - The GAMP® 5 Approach" and save up to € 590,-

Computerised System Validation: The GAMP 5 Approach

Vienna, Austria

26-28 April 2023

Computerised System Validation: The GAMP 5 Approach Book together with the course "Computerised System Validation - Introduction to Risk Management" and save up to € 590,-

The Responsible Person for Good Distribution Practice (GDP)

Vienna, Austria

3/4 May 2023

The Responsible Person for Good Distribution Practice (GDP)

Vienna, Austria

23-25 May 2023

Analytical Instrument Qualification Practical Approaches for USP General Chapter <1058> Compliance in the QC Laboratory

Vienna, Austria

6/7 June 2023

KPIs and Quality Metrics How to foster Continual Quality Improvement

GMP and Quality Requirements for Radiopharmaceuticals

Vienna, Austria

13/14 June 2023

GMP and Quality Requirements for Radiopharmaceuticals

Vienna, Austria

28/29 June 2023

Lean GMP Systems Compliance – Efficiency – Quality

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

Vienna, Austria

6/7 September 2023

Drug Master File Procedures in the EU, the US and Japan Taking into account the guidance on metal impurities (ICH Q3D) and genotoxic impurities (ICH M7)

Vienna, Austria

19-21 September 2023

Lab Data Integrity Master Class Case Studies, Best Practices, Practical Solutions for GMP Laboratories

FDA Compliance in Analytical Laboratories

Vienna, Austria

27-29 September 2023

FDA Compliance in Analytical Laboratories How to implement cGMP requirements in the everyday practice of quality control laboratories

Vienna, Austria

10/11 October 2023

Handling Changes and Variations

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GMP Training Courses - Vienna

Computerised System Validation: Introduction to Risk Management + GAMP 5 Approach Learn How to Plan, Implement and Document Effectively Computer Validation Activities

Computerised System Validation: Introduction to Risk Management Book together with the course "Computerised System Validation - The GAMP® 5 Approach" and save up to € 590,-

Computerised System Validation: The GAMP 5 Approach Book together with the course "Computerised System Validation - Introduction to Risk Management" and save up to € 590,-

The Responsible Person for Good Distribution Practice (GDP)

Analytical Instrument Qualification Practical Approaches for USP General Chapter <1058> Compliance in the QC Laboratory

KPIs and Quality Metrics How to foster Continual Quality Improvement

GMP and Quality Requirements for Radiopharmaceuticals

Lean GMP Systems Compliance – Efficiency – Quality

Drug Master File Procedures in the EU, the US and Japan Taking into account the guidance on metal impurities (ICH Q3D) and genotoxic impurities (ICH M7)

Lab Data Integrity Master Class Case Studies, Best Practices, Practical Solutions for GMP Laboratories

FDA Compliance in Analytical Laboratories How to implement cGMP requirements in the everyday practice of quality control laboratories

Handling Changes and Variations

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