Regulations Governing Control of Importation and Exportation of Pharmaceutical Products and Medical Devices.
Country
Type of law
Regulation
Abstract
The purpose of these Regulations, which are composed by 5 Chapters, is described by Chapter 1. It is to provide a legal framework for the effective and efficient control of importation and exportation of pharmaceutical products and medical devices and provide a transparent, non-discriminatory process their importation and/or exportation.
Chapter 2 covers various aspects of importation and exportation of pharmaceutical products and medical devices, including authorizations, licences, requirements and eligibility to obtain those etc.
Chapter 3 regulates the refusal, validity, suspension and withdrawal of an import/export authorization while Chapter 4 regulates the renewal and variation of an authorization.
Miscellaneous provisions, at Chapter 5, terminate the document.
Chapter 2 covers various aspects of importation and exportation of pharmaceutical products and medical devices, including authorizations, licences, requirements and eligibility to obtain those etc.
Chapter 3 regulates the refusal, validity, suspension and withdrawal of an import/export authorization while Chapter 4 regulates the renewal and variation of an authorization.
Miscellaneous provisions, at Chapter 5, terminate the document.
Attached files
Long title of text
Regulations Governing Control of Importation and Exportation of Pharmaceutical Products and Medical Devices.(Rwanda FDA law N°. 003/2018 of 09/02/2019, Article 9).
Date of text
Repealed
No
Publication reference
Doc. Ref.No.: CBD/TRG/002 Rev _I
Source language
English
Legislation Amendment
No