Regulatory Rapporteur June 2012

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Front Cover
Volume 9 Issue 6

In This Issue

  • Focus - Benefit–risk
  • PLUS
  • Nonclinical aspects of biosimilar development – A regulatory perspective
  • Changes to EN 60601-1 and how to maintain MDD compliance
  • Nutraceuticals and functional food regulations in key emerging markets: Part 2 – Specifics

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Regulatory Rapporteur June 2012MembersFull Issue4MBPDF
Evaluating benefit-risk: An Agency PerspectivePublic2MBPDF
Evaluating benefit–risk during and beyond drug development: An Industry ViewPublic915KBPDF