Guidelines for the regulatory assessment of medicinal products for use in self-medication

http://whqlibdoc.who.int/hq/2000/WHO_EDM_QSM_00.1.pdf

It suggests criteria and methods which drug regulatory agencies can employ in determining the suitability of medicinal products for use in self-medication, and provides guidance on documentation for new active substances, never marketed as prescription medicines, to accompany applications for self-medication marketing authorization. Document in pdf format; Acrobat Reader required.

Originator(s): World Health Organization. Essential Drugs and Medicine Policy - WHO / EDM
Resource added in: 07/01/2002
Available languages: English
Pharmaceutical Preparations, Self Medication, Legislation, Drug
  • Share
  • Suggest tag
    [X]
    Suggestions
    Separated by comma
    [X]
    Thank you for your suggestion.
    Communication problem. Please try again later.
  • Report error
    [X]
    Reason
    New Link (Optional)
    [X]
    Thank you for your report.
    Communication problem. Please try again later.
comments powered by Disqus

More related