Development Regulatory Affairs for Oncology Medicinal Products 2015

  • 30 Jun 2015
  • Webinar

Description

Topics
  • Regulatory strategy in oncology
  • Covered in the Session:
  • Small patients populations
  • One pivotal study
  • Faster approval pathways
  • Scientific advice
Who should Attend
  • Project Managers
  • Senior management
  • CRAs and CRCs
  • Medical writers
  • Investigators
  • QA / Compliance personnel
  • QA / QC Auditors and Staff
  • Clinical Research Scientists
  • Consultants

Past Events

Important

Please, check "Development Regulatory Affairs for Oncology Medicinal Products" official website for possible changes, before making any traveling arrangements

Event Categories

Education: Training
Health & Medicine: Medical laboratories, Medical technology
Science: Environmental sciences, Health sciences

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