Follow via Facebook
Follow via Twitter
.
Saturday, 15 August 2020
Medicines Control Authority of Zimbabwe
Home
About Us
Who we are
The Board and Its Commitee
Careers @ MCAZ
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
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
.
Saturday, 15 August 2020
Frequently Asked Questions - Licencing and Enforcement
FAQs - Licencing and Enforcement
31. What are the guidelines for setting up a manufacturing plant in Zimbabwe?
32. What are the requirements for setting up a plant for manufacturing Pharmacopeia preparations?
33. Where do I get information for GMP inspection fees?
34. How long is the validity of the GMP approval?
35. Does MCAZ inspect my facility if the site is approved by WHO or other SRAs?
Copyright © 2016 Medicines Control Authority of Zimbabwe. All Rights Reserved. Terms of Use | Privacy Policy
