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 * Public & Online Training
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 * Contact

 * Public & Online Training
 * In-house Training
 * Our Clients
 * Our Trainers
 * Contact




PUBLIC & ONLINE TRAINING

 1. Symmetric
 2. Public & Online Training

 * All
 * Pharma & Biotech
 * Process Industry
 * Medical Devices

Paediatric Drug Development & Clinical Trials
9. September 2021
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
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
Paediatric Drug Development & Clinical Trials
9. September 2021
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
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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