Biopharmaceuticals to Cell & Gene Therapies
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A Beginner's Guide to Biopharmaceutical Manufacturing
Bioprocess and Analytical Method Development
Bioprocess Characterisation, Qualification and Validation
Tech Transfer for Biopharmaceutical Manufacturing
A Practical Guide to Single Use Technologies
Upstream Process Development
Scale-Up and Validation
Biosimilar Development Strategies
Analysing Bioassays and Immunoassays
Continuous Manufacturing and Bioprocessing
Comparability for Biologics
Regulatory and Compliance Requirements for CMC Analytical Studies
Methods and Reference Standards for CMC Analytical Studies
Development and Regulatory Challenges for Cell & Gene Therapies
Applying Big Data Analytics in Bioprocessing
Good Laboratory Practice (GLP)
Good Manufacturing Practice (GMP)
Product Specifications, Stability, Comparability and Similarity for CMC Analytical Studies
Bioreactors in Biotech: Strategies for Selection and Optimization
Aseptic GMP for Cell & Gene Therapies
Design of Experiments
Quality by Design
Regulatory Affairs for Biopharmaceuticals
Global Regulatory and Quality Challenges: Making Changes in Biopharmaceutical Processes
Viral Safety and Clearance in Bioprocessing
Viral Vectors in Cell & Gene Therapy
CDMO Oversight in Biomanufacturing
Investment for Biotech
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