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Guidelines and Forms

ETHIOPIA

Laboratory Requisition Form

GMP inspection requirements for MAA 120608

API Reference Standards Comms 130125

GMP Guideline for pharmaceutical products 2014

Guideline for Registration of Medical devices 140901

Guideline for Registration of Medicines 140601

Post-Approval Variation Guidelines 1512xx

GDP, GSP and Recall Guideline 1509xx

Guidance on biowaiver of in vivo bioequivalence requirements 1512xx

Samples Submision Form 030.001

Service Fee Form xxxxxx

Last updated:Monday, September 25, 2017
Information presented here is subject to change. Should you have additional inputs / insights to contribute please contact info@ipasa.co.za.
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