GMP Training Courses - Berlin

Name: Process Validation in the light of the revised Annex 15 and FDA Requirement
Start: 2020-10-06
End: 2020-10-06
Location: Process Validation in the light of the revised Annex 15 and FDA Requirement

Berlin, Germany

6/7 October 2020

Process Validation in the light of the revised Annex 15 and FDA Requirement

Product Transfer - Organisation of a GMP-compliant Site Change

Berlin, Germany

20-22 October 2020

Product Transfer - Organisation of a GMP-compliant Site Change

Design Control for Drug - Device Combination Products

Berlin, Germany

21-23 October 2020

Design Control for Drug - Device Combination Products

Blood and Plasma – Audits and Inspections

Berlin, Germany

27/28 October 2020

Blood and Plasma – Audits and Inspections

Launch Conference <br>Final version: ECA's Integrated Qualification and Validation Guide <br>Im Auftrag der ECA Academy

Berlin

27./28. Oktober 2020

Launch Conference Final version: ECA's Integrated Qualification and Validation Guide Im Auftrag der ECA Academy

Berlin, Germany

3-5 November 2020

Lab Data Integrity Master Class

Berlin, Germany

10/11 November 2020

SAP: Validation and GMP Compliance

Validation of Analytical Test Procedures & Measurement Uncertainty

Berlin, Germany

23-25 November 2020

Validation of Analytical Test Procedures & Measurement Uncertainty

Data Integrity and Good Documentation Practice

Berlin, Germany

24-26 November 2020

Data Integrity and Good Documentation Practice

15th QP Forum Pre-Conference Sesssion: Specific Requirements for IMPs

Berlin, Germany

25 November 2020

15th QP Forum Pre-Conference Sesssion: Specific Requirements for IMPs

15th QP Forum Half Day Pre-Conference Session: Human Error

Berlin, Germany

25 November 2020

15th QP Forum Half Day Pre-Conference Session: Human Error

15th QP Forum Half Day Pre-Conference Session: Serialisation re-revisited

Berlin, Germany

25 November 2020

15th QP Forum Half Day Pre-Conference Session: Serialisation re-revisited

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GMP Training Courses - Berlin

Process Validation in the light of the revised Annex 15 and FDA Requirement

Product Transfer - Organisation of a GMP-compliant Site Change

Design Control for Drug - Device Combination Products

Blood and Plasma – Audits and Inspections

Launch Conference Final version: ECA's Integrated Qualification and Validation Guide Im Auftrag der ECA Academy

Lab Data Integrity Master Class

SAP: Validation and GMP Compliance

Validation of Analytical Test Procedures & Measurement Uncertainty

Data Integrity and Good Documentation Practice

15th QP Forum Pre-Conference Sesssion: Specific Requirements for IMPs

15th QP Forum Half Day Pre-Conference Session: Human Error

15th QP Forum Half Day Pre-Conference Session: Serialisation re-revisited

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