Public Health Act, 2012 (Act 851)
Section 125: (1) A local representative for a regulated product shall be appointed by the relevant body.
(2) The local representative
(a) shall monitor the safety of the product granted marketing approval, and(b) shall report an adverse effect or event to the Authority during the period under which the product is registered.
(3)The Authority shall continually monitor the safety of the products regulated under this Act by analysis of the adverse effect or event reports and by any other means and take appropriate regulatory action when necessary.
Subject : Drugs, Herbal Medicinal products, Cosmetics, Medical Devices and Household Chemical Substances (food and drugs)
Procedure to Follow
Not Avaiable
Responsible Institution
Ministry of Trade, Agribusiness and Industry
Ministries
- Email: info@moti.gov.gh
- Website: www.moti.gov.gh
- GPS: GA-144-0150
- Telephone: 0500073887
Relevant Forms to Download
Not Available
Online System
Link Unavailable
Fees/ charges
Not Avaiable
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