Follow via Facebook
Follow via Twitter
.
Friday, 03 February 2023
Medicines Control Authority of Zimbabwe
Home
About Us
Who we are
The Board and Its Commitee
Careers @ MCAZ
Tenders
Corporate Governance
Privacy Policy
How We Regulate
Evaluation/Registration
Licensing and Enforcement
Overview
Licensing
Inspections
Import and Export
Product Defects and Recalls
Notifications
Statistics
Frequently Asked Questions
Enquiries
Pharmacovigilance and Clinical Trials
Current Projects
Pharmacovigilance Centre
Publications
Clinical Trials
WHO Pharmacovigilance Toolkit
Laboratory Services
Medical Devices
Legal and Corporate Affairs
Quality Assurance
Safety News
Vaccine Safety
Downloads
Online Services
Online Registers
Online Applications
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
.
Friday, 03 February 2023
Frequently Asked Questions - Medical Devices
FAQs - Medical Devices
11. Who is responsible for the cost of a GMP inspection of a manufacturer?
12. Can I distribute my gloves if the manufacturer has not been inspected?
13. If my products fail analysis what happens to the consignment?
14. Are there storage conditions that I have to adhere to when distributing my products?
15. What are the key labelling requirements for gloves/condoms?
16. Do I get a certificate of approval when I register my products?
17. How long is the product approval valid for?
18. Do I need to have a registered business for me to distribute gloves?
19. What are the consequences of distributing unapproved products?
20. What payment methods are available for services at MCAZ?
Copyright © 2016 Medicines Control Authority of Zimbabwe. All Rights Reserved. Terms of Use | Privacy Policy