The Drug Development Path - From R&D to Commercialization - Webinar by GlobalCompliancePanel 2011

  • 04 Oct 2011
  • Webinar

Description

The Drug Development Process - From R&D to Commercialization is a webinar that covers topics such as:

  • The purpose of Pre-clinical studies
  • The transition from discovery to development
  • Milestones on The "Dual Path" to Drug Commercialization
  • The four major clinical phases (1-4) in the drug development process and the rationale for each with key deliverables
  • Overview of the key government regulations that impact the development process (Code of Federal Regulations and ICH)
  • Where do IND and NDA fit into the process
  • The criticality of effective project management for cross-functional teams during the development process with special focus on managing activities performed by contract manufactures, labs and suppliers
  • Designing the drug with the patient and regulations in mind

The Drug Development Process - From R&D to Commercialization brings together Clinical monitors and research associates, Research & development scientists, Statisticians & data management professionals, Medical and clinical investigators and study coordinators, Regulatory Affairs Professionals, CMC/pharmaceutical research professionals, Senior sales managers, Project Managers, Program Management and Analytical Development.

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Important

Please, check "The Drug Development Path - From R&D to Commercialization - Webinar by GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Health & Medicine: Medical device, Pharma

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