Public & Online Training

Process Scale-up, Validation and Technology Transfer for Biologics

20. September 2021

Using RWE to Accelerate Market Access in Rare Diseases

27. September 2021

Bioequivalence and IVIVC

4. October 2021

Process Scale-up, Validation & Technology Transfer

11. October 2021

Process Design, Scale-up and Technology Transfer for Medical Devices

18. October 2021

CMC Regulatory Compliance for Biological Drug Products

18. October 2021

Value Added Medicines / Scientific, Regulatory and IP Analysis

18. October 2021

Stability Testing for Biological Drug Products

20. October 2021

Process Scale-up & Tech Transfer for Injectables

25. October 2021

Aseptic Fill & Finish for Biologics

8. November 2021

Viral Safety for Biologics

8. November 2021

Process Scale-up, Validation and Technology Transfer for Biologics (US Edition)

22. November 2021

Orphan Drugs Clinical Trials

22. November 2021

Accelerating of Gene & Cell Therapy

22. November 2021

Advanced Industrial Process and Unit Operations Scale-up

24. November 2021

Paediatric Drug Development & Clinical Trials

Pharmaceutical Quality: QRM, CAPA & Root Cause Analysis

Project Management for Generics

GMP and Validation for Equipment Suppliers

Virtual Dissolution / Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers

Patient Centricity: PROs & Clinical Outcomes Assessments

Development of Generic Solid Immediate Release Dosage Forms / Formulation and Analytical Method Development

Process Scale-up, Validation and Technology Transfer for Biologics

20. September 2021

Using RWE to Accelerate Market Access in Rare Diseases

27. September 2021

Bioequivalence and IVIVC

4. October 2021

Process Scale-up, Validation & Technology Transfer

11. October 2021

CMC Regulatory Compliance for Biological Drug Products

18. October 2021

Value Added Medicines / Scientific, Regulatory and IP Analysis

18. October 2021

Stability Testing for Biological Drug Products

20. October 2021

Process Scale-up & Tech Transfer for Injectables

25. October 2021

Aseptic Fill & Finish for Biologics

8. November 2021

Viral Safety for Biologics

8. November 2021

Process Scale-up, Validation and Technology Transfer for Biologics (US Edition)

22. November 2021

Orphan Drugs Clinical Trials

22. November 2021

Accelerating of Gene & Cell Therapy

22. November 2021

Paediatric Drug Development & Clinical Trials

Pharmaceutical Quality: QRM, CAPA & Root Cause Analysis

Project Management for Generics

GMP and Validation for Equipment Suppliers

Virtual Dissolution / Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers

Patient Centricity: PROs & Clinical Outcomes Assessments

Development of Generic Solid Immediate Release Dosage Forms / Formulation and Analytical Method Development

Advanced Industrial Process and Unit Operations Scale-up

24. November 2021

Process Design, Scale-up and Technology Transfer for Medical Devices

18. October 2021

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