This Guideline provides regulatory information on licensing of new pharmaceutical manufacturing plants and the steps involved to obtain the same. It also contains details on inspections in respect of good manufacturing practices which includes new inspections, risk based routine inspections, exemptions and fees. A list of reference guideline documents of the Word Health Organization (WHO) such as the WHO good manufacturing practices for pharmaceutical products: main principles, are included in the Guideline.
Zimbabwe · 2019-11-01