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Consulting
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Training Courses
In-house Training
Consulting
Clients
Trainers
Blog
About us
Contact
Training Courses
In-house Training
Consulting
Clients
Trainers
Blog
About us
Contact
Events
Symmetric
Events
Public & Online Training
Pharma & Biotech
CMO Contracting, Oversight and Value Optimisation
Pharma & Biotech
1. October 2024
Contamination Control Strategy
ANNEX 1
Pharma & Biotech
2. October 2024
CMC Regulatory Compliance for Biological Drug Products
Pharma & Biotech
2. October 2024
Development and Validation of Bioassays
Pharma & Biotech
14. October 2024
Process Scale-up, Validation and Technology Transfer for Biologics
Pharma & Biotech
14. October 2024
Mastery in mRNA Manufacturing: Navigating International Regulations & Best Practices
Pharma & Biotech
15. October 2024
Project Management for Generics
Pharma & Biotech
21. October 2024
Extractables and Leachables Control Strategies
Pharma & Biotech
22. October 2024
Paediatric Drug Development & Clinical Trials
Pharma & Biotech
24. October 2024
Aseptic Processing in Manufacture of Sterile Products & ATMPs
Pharma & Biotech
28. October 2024
Lipid Based Formulations
Pharma & Biotech
28. October 2024
Process Scale-up, Validation & Technology Transfer
Pharma & Biotech
28. October 2024
CMC Statistics
Pharma & Biotech
4. November 2024
Aseptic Fill & Finish of Biologics
Pharma & Biotech
9. December 2024
Drug-Device Combination Products: Quality & Regulatory Requirements
Medical Devices
Pharma & Biotech
Public & Online Training
10. December 2024
Bioequivalence and IVIVC
Pharma & Biotech
11. December 2024
CMC and Regulatory Requirements for Inhalation Drug Products
Medical Devices
Pharma & Biotech
Public & Online Training
11. February 2025
Process Scale-up & Tech Transfer for Injectables
Pharma & Biotech
10. March 2025
Cleaning Validation in Pharma
CMC Regulatory Compliance for ATMPs
Annex 1 Compliance: Challenges, Solutions and International Impact (EU GMP & PIC/S)
GMP Lead Auditor
Technology Transfer for Pharma & Biotech
CMC/Regulatory Affairs for Nucleic Acids
Orphan Drugs Clinical Trials
Clinical Trial Design & Quality
Development of Solid Generic Formulations
Strategic Marketing for CDMO Industry
Quality Requirements for Solids
Analytical Method Development and Validation
Pharma & Biotech Stability Testing
Pricing and Market Access of ATMPs
Value Added Medicines / Scientific, Regulatory and IP Analysis
Statistical Methods Across the Product/ Process Lifecycle
Specifications for Small Molecule Drug Products
Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers
Pharmaceutical Quality: QRM, CAPA & Root Cause Analysis
Development of Generic Solid Immediate Release Dosage Forms / Formulation and Analytical Method Development
Advancing Real-World Evidence Generation for Causal Inference
Pharma & Biotech
2. October 2023
Real-World Evidence in Rare Diseases: Accelerating Market Access
Stability Testing of Biological Drug Products
Pharmaceutical Data Integrity
Change Management for Medical Affairs
Good Manufacturing Practices in API Production: How to Implement ICHQ7
Quality Requirements for Biologics
Mitigating Immunogenicity Risk
Signal Detection and Management in Pharmacovigilance
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