Regulatory Rapporteur Sep 2012

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Front Cover
Volume 9 Issue 9

In This Issue

  • FOCUS - Chemistry, Manufacturing and Controls
  • PLUS
  • The evolution of QbD – from inception to maturity in 2012
  • A case for standardising regulatory excipient evaluation
  • Towards improved patient safety – issues and solutions in implementation of the new pharmacovigilance legislation

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TitleDownloadCategorySizeFile
Regulatory Rapporteur Sep 2012MembersFull Issue3MBPDF
The evolution of QbD – from inception to maturity in 2012Public934KBPDF
A case for standardising regulatory excipient evaluationMembers897KBPDF
Getting good medicines to patients and keeping them thereMembers778KBPDF
Key changes to requirements for post-market clinical follow-up studiesMembers811KBPDF
The Veterinary Medicines ExchangeMembers779KBPDF