Guideline Complementary Medicines – Approved by Registration Committee
Guideline Complementary Medicines – Approved by Registration Committee
Size: 942 KB
Published: July 11, 2025
MCAZ-EVR-GL-13 Guildelines on Submission of Documentation for Registration of Veterinary Vaccines
MCAZ-EVR-GL-13 Guildelines on Submission of Documentation for Registration of Veterinary Vaccines
Size: 275 KB
Published: October 30, 2025
MCAZ-EVR-GL-12 Guidelines for Conducting Trials for Cattle Acaricides in Zimbabwe
MCAZ-EVR-GL-12 Guidelines for Conducting Trials for Cattle Acaricides in Zimbabwe
Size: 450 KB
Published: October 30, 2025
MCAZ-EVR-GL09 Rev 0_July 2024 Guidelines on Veterinary Good Clinical Practice
MCAZ-EVR-GL09 Rev 0_July 2024 Guidelines on Veterinary Good Clinical Practice
Size: 248 KB
Published: July 12, 2025
MCAZ-EVR-GL-08 Rev 0_Feb 2024 Guidelines on Pharmacovigilance of Veterinary Medicinal Products
MCAZ-EVR-GL-08 Rev 0_Feb 2024 Guidelines on Pharmacovigilance of Veterinary Medicinal Products
Size: 475 KB
Published: July 12, 2025
MCAZ-EVR-GL-07 Rev 0_February 2024 Guidelines on Variations for Veterinary Medicinal Products
MCAZ-EVR-GL-07 Rev 0_February 2024 Guidelines on Variations for Veterinary Medicinal Products
Size: 668 KB
Published: July 12, 2025

Human Medicines Guidelines

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EVRF 10 Rev 6_July 2026 Meeting Request Form
EVRF 10 Rev 6_July 2026 Meeting Request Form
Size: 178KB
EVRF 30 Rev 03_May 2024_APPLICANTS_SCREENING CHECKLIST FOR REGISTRATION OF HUMAN MEDICINES
EVRF 30 Rev 03_May 2024_APPLICANTS_SCREENING CHECKLIST FOR REGISTRATION OF HUMAN MEDICINES
Size: 360KB
EVRF 10 Rev 5_July 2024 Meeting Request Form
EVRF 10 Rev 5_July 2024 Meeting Request Form
Size: 323KB
EVRF 05 Rev 07_November 2025 – BIOPHARMACEUTICS CLASSIFICATION SYSTEM (BCS) BASED BIOWAIVER INFORMATION FORM
EVRF 05 Rev 07_November 2025 – BIOPHARMACEUTICS CLASSIFICATION SYSTEM (BCS) BASED BIOWAIVER INFORMATION FORM
Size: 405KB
EVRF 07 Rev 06_November 2025 – ADDITIONAL STRENGTH BIOWAIVER INFORMATION FORM
EVRF 07 Rev 06_November 2025 – ADDITIONAL STRENGTH BIOWAIVER INFORMATION FORM
Size: 348KB
EVRF 30 Rev 03_May 2024_APPLICANTS_SCREENING CHECKLIST FOR REGISTRATION OF HUMAN MEDICINES
EVRF 30 Rev 03_May 2024_APPLICANTS_SCREENING CHECKLIST FOR REGISTRATION OF HUMAN MEDICINES
Size: 70KB
Published: March 2, 2026
EVRF86_Rev 0 Feb 2026_ APPLICANT’S SCREENING CHECKLIST FOR APPROVAL OF COMPLEMENTARY MEDICINES
EVRF86_Rev 0 Feb 2026_ APPLICANT’S SCREENING CHECKLIST FOR APPROVAL OF COMPLEMENTARY MEDICINES
Size: 105KB
Published: March 2, 2026
EVRF 85 Rev 0_September 2025 APPLICANTS SCREENING CHECK-LIST FOR SUBMISSION OF A DOSSIER FOR REGISTRATION OF A VETERINARY VACCINE
EVRF 85 Rev 0_September 2025 APPLICANTS SCREENING CHECK-LIST FOR SUBMISSION OF A DOSSIER FOR REGISTRATION OF A VETERINARY VACCINE
Size: 125KB
EVRF 79 Rev 0_July 2024-QUALITY OVERALL SUMMARY
EVRF 79 Rev 0_July 2024-QUALITY OVERALL SUMMARY
Size: 585kb
EVRF 56 Rev 1_February 2024 Application form for major minor variations and immediate notifications
Size: 265kb
EVRF 55 Rev 1_February 2024 Application form for annual notifications
Size: 288kb
EVRF 34_Rev 04 May_2024_APPLICANT’S SCREENING CHECKLIST FOR REGISTRATION OF HUMAN BIOLOGICAL MEDICINES
Size: 334kb
EVRF 03 Rev 05_November 2025 – BIOEQUIVALENCE TRIAL INFORMATION FORM
Size: 315KB
EVRF 03 Rev 05_November 2025 – BIOEQUIVALENCE TRIAL INFORMATION FORM
Size: 388KB
EVRF 03 Rev 05_November 2025 – BIOEQUIVALENCE TRIAL INFORMATION FORM
Size: 391KB
EVRF56/Rev 1 February 2024/Application form for major, minor variations and intermediate notifications
EVRF56/Rev 1 February 2024/Application form for major, minor variations and intermediate notifications
Size: 128 KB
Published: July 25, 2025
EVRF55/Rev 1 February 2025/Application for Annual notifications
EVRF55/Rev 1 February 2025/Application for Annual notifications
Size: 127 KB
Published: July 25, 2025
EVRF44/Rev 4 April 2025/Status update request form
EVRF44/Rev 4 April 2025/Status update request form
Size: 101 KB
Published: July 25, 2025
EVRF34/Rev 4 May 2024/Applicants screening checklist for Biologics
EVRF34/Rev 4 May 2024/Applicants screening checklist for Biologics
Size: 120 KB
Published: July 25, 2025
REGISTRATION CERTIFICATE_MC16_FORM
REGISTRATION CERTIFICATE_MC16_FORM
Size: 38KB
EVRF 79 Rev 0_July 2024 – QUALITY OVERALL SUMMARY
EVRF 79 Rev 0_July 2024 – QUALITY OVERALL SUMMARY
Size: 110KB
EVRF 73 Rev 1_May 2025-MCAZ QUALITY INFORMATION SUMMARY
EVRF 73 Rev 1_May 2025-MCAZ QUALITY INFORMATION SUMMARY
Size: 103KB
MC8 – Application for registration of medicine 2016
MC8 – Application for registration of medicine 2016
Size: 319KB
Complementary medicines form CM1
Complementary medicines form CM1
Size: 152KB
EVR 34_ SOP for Issuing a letter for no objection , searching and retreiving of documents and post -Dossier Submission meeting requests for scientific advise
EVR 34_ SOP for Issuing a letter for no objection , searching and retreiving of documents and post -Dossier Submission meeting requests for scientific advise
Size: 517KB
Published: February 26, 2026
EVR 33_SOP for issuing a marketing authorisation certificate of a medicinal product (Human Complementarty medicines)
EVR 33_SOP for issuing a marketing authorisation certificate of a medicinal product (Human Complementarty medicines)
Size: 1.2MB
Published: February 24, 2026
EVR 28 _May 2024 SOP for Evaluation for an Application for Re-registration to a Registered Medicine
EVR 28 _May 2024 SOP for Evaluation for an Application for Re-registration to a Registered Medicine
Size: 397KB
Published: February 24, 2026
EVR 32_ SOP for Issuing a marketing authorisation certificate of a medicinal product (Veterinary Medicines)
EVR 32_ SOP for Issuing a marketing authorisation certificate of a medicinal product (Veterinary Medicines)
Size: 5KB
Published: February 24, 2026
EVR 21_SOP FOR HANDLING A RETURNED REGISTRATION OR APPROVAL CERTIFICATE OF A PRODUCT
EVR 21_SOP FOR HANDLING A RETURNED REGISTRATION OR APPROVAL CERTIFICATE OF A PRODUCT
Size: 3.4MB
Published: February 24, 2026
EVR 25_Rev 3 September 2025_SOP for publishing a Summary of Product characteristics (SmPC)
EVR 25_Rev 3 September 2025_SOP for publishing a Summary of Product characteristics (SmPC)
Size: 653KB
Published: February 24, 2026
EVR 20__ SOP for Issuing a WHO-Type certificate of Pharmaceutical Product
EVR 20__ SOP for Issuing a WHO-Type certificate of Pharmaceutical Product
Size: 547KB
Published: February 24, 2026
EVR 16_ SOP for Correspondence with clients
EVR 16_ SOP for Correspondence with clients
Size: 482KB
Published: February 24, 2026
EVR 15_ SOP for Evaluation of Application for emergency use authorisation of medical products
EVR 15_ SOP for Evaluation of Application for emergency use authorisation of medical products
Size: 461KB
Published: February 24, 2026
EVR 10_ SOP for preparation of information for issuing of a gazette notice
EVR 10_ SOP for preparation of information for issuing of a gazette notice
Size: 490KB
Published: February 24, 2026
EVR 07_SOP for submission of samples to the laboratory
EVR 07_SOP for submission of samples to the laboratory
Size: 570KB
Published: February 24, 2026
EVR 03_ SOP for issuing a registration certificate of a medicinal product (Human Allopathic Medicines)
EVR 03_ SOP for issuing a registration certificate of a medicinal product (Human Allopathic Medicines)
Size: 5.9MB
Published: February 24, 2026
EVR-RF-01 Rev 1_March 2026 Reliance Framework for Medicines Approved by NRAs Under MoU with MCAZ
EVR-RF-01 Rev 1_March 2026 Reliance Framework for Medicines Approved by NRAs Under MoU with MCAZ
Size: 326 KB
Published: April 3, 2026
EVR-RF-03 Rev 0_March 2026 Recognition Framework For Medicines
EVR-RF-03 Rev 0_March 2026 Recognition Framework For Medicines
Size: 311KB
Published: April 3, 2026
EVR PERFORMANCE REVIEW
EVR PERFORMANCE REVIEW
EVR-3rd-stakeholders-29.11.2024_Circular-21-of-2024
EVR-3rd-stakeholders-29.11.2024_Circular-21-of-2024
Size: 330KB
EVR-3rd-stakeholders-29.11.2024_Processing-application-in-2025_GRM
EVR-3rd-stakeholders-29.11.2024_Processing-application-in-2025_GRM
Size: 392KB
EVR-2nd-stakeholders-meeting_Implementation-of-Re-registration-MA-Renewals-2025-to-2027_NMs
EVR-2nd-stakeholders-meeting_Implementation-of-Re-registration-MA-Renewals-2025-to-2027_NMs
Size: 538KB
EVR-2nd-Stakeholders-meeting_Circular-26-of-2023_-GRM
EVR-2nd-Stakeholders-meeting_Circular-26-of-2023_-GRM
Size: 741KB
WHO formal benchmarking of Medicines Control Authority of Zimbabwe
WHO formal benchmarking of Medicines Control Authority of Zimbabwe
Size: 1MB
Regulatory Perfomance Indicators Based on Circular 26 of 2023
Regulatory Perfomance Indicators Based on Circular 26 of 2023
Size: 2MB
MCAZ Feedback on the new system of processing applications for registration
MCAZ Feedback on the new system of processing applications for registration
Size: 2MB
Implementation plan for grouped variations and variations notifications
Implementation plan for grouped variations and variations notifications
Size: 360KB
Hybrid Complementary Medicine Stakeholders engagement_Statistics
Hybrid Complementary Medicine Stakeholders engagement_Statistics
Size: 2MB
MCAZ Comps Stakeholder Meeting_Common Deficiencies
MCAZ Comps Stakeholder Meeting_Common Deficiencies
Size: 1MB
Presentation on dipping trial guidelines
Presentation on dipping trial guidelines
Size: 833KB
Vaccine guidelines training
Vaccine guidelines training
Size: 254KB
Hybrid Complementary Medicine Stakeholders_Process updates
Hybrid Complementary Medicine Stakeholders_Process updates
Size: 4MB
EVR-1st Stakeholders Meeting 25.04.2024 Deficiencies noted in registration applications NMs
EVR-1st Stakeholders Meeting 25.04.2024 Deficiencies noted in registration applications NMs
Size: 13KB
Published: November 12, 2025
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