Biosimilars and Follow-On Biologics Americas

Biosimilars and Follow-On Biologics Americas is a conference that covers topics such as:

  • Clinical and preclinical challenges in the development of biosimilars
  • Global regulations and guidelines for Biosimilars including variations and new developments
  • Conducting trials, assessing immunogenicity and pharmacovigilance
  • Challenges encountered with specific product manufacturing
  • Issues in developing biosimilars mAbs
  • CMC requirements in order to produce high quality similar biologic product
  • How the BRIC market is dealing with Biosimilars

Biosimilars and Follow-On Biologics Americas brings together Directors, VPs, Managers and Heads from:

  • Follow on Biologics/Follow on Proteins/Biosimilars
  • Biologics/Biotechnology/ Biogenerics
  • Biopharmaceuticals/ Biotherapeutics
  • Legal Affairs
  • Intellectual property
  • Pricing and Reimbursement
  • Clinical Immunology
  • Regulatory Compliance
  • R & D
  • Preclinical and Clinical Development
  • New Product Development
  • Quality Affairs/ Quality Control
  • Principal Scientist
  • Pharmacovigilance
  • Chief Scientific Officer
  • Drug Safety & Risk Management
  • Health Economics
  • Process Control and Analytical Technologies
  • Business Development
  • Commercial Affairs
  • Marketing & sales
  • Intellectual Property
  • Legislation and Policy Advice
  • Business Development
  • Licensing
  • Manufacturing
  • APIs
  • Bioequivalence
  • Drug and Safety Assessment
  • Market Strategy
  • Regulatory Affairs

Future Events

Biosimilars and Follow-On Biologics Americas 2020

Important

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

Prices are for evaluation only.

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