Regulatory Rapporteur January 2013

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Front Cover
Volume 10 Issue 1

In This Issue

  • FOCUS - Biotechnology
  • PLUS
  • Healthcare 'apps' as medical devices?
  • The new pharmacovigilance master file format
  • Concerns on veterinary legislation revision

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Regulatory Rapporteur January 2013MembersFull Issue3MBPDF
Considerations in the clinical development of biotech medicinesPublic987KBPDF
8th Annual Regulation of Veterinary Medicines in Europe ConferenceMembers970KBPDF
Challenges in ensuring continuity of supply for globally registered biotech productsMembers1MBPDF
Global biosimilars - available guidance and associated challengesMembers1013KBPDF
Marketing authorisation holder strategy for the new pharmacovigilance legislationMembers976KBPDF
When does healthcare stand-alone software become a medical device?Members1MBPDF