Follow via Facebook
Follow via Twitter
.
Thursday, 12 December 2019
Medicines Control Authority of Zimbabwe
Home
About Us
Who we are
The Board and Its Commitee
Careers @ MCAZ
Corporate Governance
How We Regulate
Evaluation/Registration
Licensing/Enforcement
Pharmacovigilance and Clinical Trials
Current Projects
Pharmacovigilance Centre
Publications
Clininal Trials
WHO Pharmacovigilance Toolkit
Laboratory Services
Medical Devices
Legal and Corporate Affairs
Quality Assurance
Safety News
Vaccine Safety
Downloads
Online Services
Online Registers
Import/Export for Registered Medicines
ADR E-Reporting
Consumer Reporting
Healthcare Professional Reporting
e-Clinical Trials
Publications
Annual Reports
Press Release
ReCore Training
ReCore Training Introduction
Evaluations and Registration
Clinical Trial Oversight
Quality Control
Contact Us
Contact Details
Locate Us on Map
.
Thursday, 12 December 2019
Frequently Asked Questions - Evaluations and Registration Division
FAQs - Evaluations and Registration Division
1. How do I access the list of registered veterinary medicines in Zimbabwe?
2. If we currently own a licence in Zimbabwe for a Veterinary Medicinal Product which is distributed by a Zimbabwean company, is it possible for another company to import this same product on permission from our company without being the registered distributor for this product?
3. What are Veterinary Section 75 applications?
4. What are the requirements for operating a Veterinary Medicines General Dealer (VMGD) outlet?
5. How do I get my medicine registered/approved?
6. How long will it take for my medicines to be registered?
7. What is the difference between applicant, principal and manufacturer?
8. Can a medicine which is not registered be found on the market in Zimbabwe?
9. Does MCAZ register medical devices such as BP machines, Glucometers and other diagnostic devices?
10. What is ZAZIBONA and how can we participate?
Copyright © 2016 Medicines Control Authority of Zimbabwe. All Rights Reserved. Terms of Use | Privacy Policy