Monday, February 11, 2013

LARC2013 Join the collaboration for improved regulation

Latin American Regulatory Conference (LARC) 2013 | May 15-16, 2013 | Bogota, Colombia
Join the collaboration for improved regulation
Registration is now open for the Latin American Regulatory Conference (LARC) 2013.
Join global regulators, industry professionals and academia to discuss the current regulatory landscape and its impact on future research and drug development at the event in Bogota, Colombia from May 15-16.
The event will focus on “Pharma-Co-Vergence” – the act of achieving pharmaceutical regulatory convergence through stakeholders’ collaboration – highlighting the true collaborative spirit of this multidisciplinary global conference.

Attendees will learn how to define the various initiatives related to global regulatory environment and their impact on the access of medicines and future R&D in Latin America, and discuss the progress of the Pan American Network for Drug Regulatory Harmonization (PANDRH) convergence process and working groups.
2012 VIDEO HIGHLIGHTS
Watch videos from last year’s Latin American conferences and get a taste of what you can expect from these insightful events in 2013.
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Featured Topics
  • Regulatory Landscape and Convergence Initiatives
  • Strengthening the Regulatory Framework
  • Efforts Underway by Convergence Initiatives
  • Reviews and Inspections
  • Ethics Committee Research in the Regions
  • Post-market Research Studies and Better Medicines
    to Influence
  • Efficacy and Effectiveness
  • Perspectives and Regulations of Pediatric Studies
  • Drug Safety, Marketing Surveillance and Quality Control Monitoring
  • Regulatory Concerns: Health Systems and Security of the Supply Chain
  • Current Regulations of Biologics and Biosimilars
  • Emerging Topics
Who Should Attend
Professionals involved in:
  • Regulatory affairs
  • Clinical research and development
  • Clinical safety and pharmacovigilance
  • Clinical trial and project management
  • Drug development and discovery
  • Medical and scientific affairs
  • Preclinical development
  • Quality assurance
  • Research and development
  • Strategic sourcing/planning
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