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Manual on the Effective Investigation and Documentation of Torture and Other Cruel, Inhuman or Degrading Treatment or Punishment
Third edition 2016
Document No. : FDA/SMC/SMD/GL-SMP/2015/05 | These guidelines are for information, guidance and strict compliance by Marketing Authorization Holders and Local Representatives of regulated products to help in the continuous safety monitoring of products granted marketing authorization in Ghana.
Interim policy guidance.
Manual for Early Implementation
Namibia guideline for submission of applications for registration of pharmaceuticals for human use in common technical document format.
6th edition