The CMC Biopharma MasterClass 3.0 covers topics such as:

  • Analytical and Formulation Development
  • Process Development Strategies
  • Process Analytical Technology
  • GMP Manufacture
  • Guidelines and Regulatory Pathways for New Biological Entities and Biosimilars

The CMC Biopharma MasterClass 3.0 brings together:

  • Stability program managers
  • QC release and stability analysts
  • Process analytical chemists and process development scientists
  • Product scientists and test method technical experts (R&D and QC)
  • GMP compliance auditors
  • Quality assurance specialists
  • Analytical and stability laboratory managers (R&D through GMP)
  • Regulatory affairs CMC authors or reviewers
  • Business managers with CMC responsibilities
  • Project managers with CMC responsibilities
  • Contract testing labs
  • Key staff from biotech academic incubators and small start-ups
  • Biopharmaceuticals, biosimilars
  • Chemistry, Manufacturing & Controls (CMC) regulatory
  • Executive and operational managers of pharmaceutical companies, packaging operations
  • Or other biologics
  • Quality
  • Engineering staff
  • Product Information Operations
  • Product Development Materials handling/management
  • Biotech companies HTAs
  • Licensing

Future Events

Past Events


Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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