Saturday, 22 February 2020
The Quality Office ensures that all activities in the organization are carried out in accordance with International Standards. It is responsible for:
1.The development and implementation of the following MCAZ Quality Management Systems:
1.1 ISO/IEC 17025:2005: the General Requirements for the Competence of Testing and Calibration Laboratories.
MCAZ is committed to providing a high quality, accurate and timeous service to all our stakeholders. We constantly seek ways to meet and improve the requirements of all our customers. Your complaints, comments, suggestions and feedback are always welcome. We assure you that we shall respond to them quickly and effectively.
Click Here to download the forms
Customer complaints and Customer feedback forms can be submitted in person at the MCAZ reception, as mail at Medicines Control Authority of Zimbabwe, 106 Baines Avenue, P O Box 10556, Harare, Zimbabwe or as email to This email address is being protected from spambots. You need JavaScript enabled to view it.
Sample Receipt forms have to be submitted in person with the samples to the MCAZ Samples Repository Office.
Inside this issue: E-Reporting Tools Safety Notifications for Fluoroquinolones and Quinolones Antibiotics Notification of a potential risk of non-melanoma skin cancer (basal cell carcinoma, squamous cell carcinoma) in patients treated...
In pursuit of promoting high ethical standards, the Authority has formulated a Code of Ethics for its employees and members of the Authority .The Authority believes that high ethical...
Southern African Development Community (SADC), as a region has harmonized medicines registration guidelines in the common technical document (CTD) format that were approved in January 2015. Nevertheless, the harmonization...
In line with the WHO guidelines on variations and other SRA guidelines, the EVR Division is updating the MCAZ Guidelines for submitting applications for Variations to Registered Medicines. The update...
Background The Medicines Control Authority of Zimbabwe (MCAZ) Regional Centre of Regulatory Excellence (ReCORE) in partnership with the European and Developing Countries Clinical Trials Partnership (EDCTP) is offering...
The Quality Policy of the Medicines Control Authority of Zimbabwe (MCAZ) is to ensure the provision of accurate and timeous services, continuously meet requirements of our customers and guarantee patient...
In this issue: MCAZ turns 20 years Basics of reporting Side Effects of medicines Electronic Adverse Drug Reaction Reporting For more information Please click here to download the Newsletter...
Increased Reporting from the Targeted Spontaneous Reporting (TSR) Programme Click here to download the 2018 Drug Information Bulletin
Download Complementary medicines applications extension - press statement
The aims of the PV policy handbook are to firstly provide a framework for a national pharmacovigilance system in Zimbabwe. Secondly, to define the pharmacovigilance activities undertaken by the Pharmacovigilance...
The Medicines Control Authority of Zimbabwe (MCAZ) as a responsible corporate citizen runs a Scholarship Fund as part of its corporate social responsibility programmes. Click here to download the...
The approved Guidelines for Advertising and Promotion of Medicines are now available. Download the Guidelines for Advertising and Promotion of Medicines