Follow via Facebook
Follow via Twitter
.
Tuesday, 15 October 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
.
Tuesday, 15 October 2019
Frequently Asked Questions - Medical Devices
FAQs - Medical Devices
1. How do I register gloves/condoms?
2. Who can register gloves/condoms?
3. What is a type of glove/condom?
4. How many pieces of gloves/Condoms should I submit as a sample for routine testing?
5. How long does it take for my product to be registered?
6. What is the cost of registration?
7. What is a clearance letter?
8. How long does it take to have a clearance letter ready and how much does it cost?
9. Does MCAZ regulate other medical devices other than condoms and gloves?
10. Can I import and distribute a product registered by another distributor?
Copyright © 2016 Medicines Control Authority of Zimbabwe. All Rights Reserved. Terms of Use | Privacy Policy
