Regulatory Rapporteur October 2010

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Front Cover
Volume 7 Issue 10

In This Issue

  • Forging new regulatory pathways
  • Biosimilar biologics
  • Adaptive trial designs

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Regulatory Rapporteur October 2010MembersFull Issue2MBPDF
An introduction to adaptive clinical trial designsPublic517KBPDF
A risk-based approach to medicinal products and medical devices – The common challenges for all stakeholdersMembers489KBPDF
Changes to the European guidance on clinical trialsMembers491KBPDF
EU regulatory updates: June–August 2010Members479KBPDF
Face the strange…ch-ch-changes: Potential FDA regulation of social mediaMembers496KBPDF
Inspiration, innovation and regulationMembers478KBPDF
Meet the regulators – Interview: Christer Backman: Lawyer, regulator, musician...Members485KBPDF
The current status of biosimilar biologics – Part 2: Practical considerations in international development through European lessons learnedMembers549KBPDF
The Medical Devices ExchangeMembers460KBPDF