The process of submitting an application for registration of a medicine is described below in detail. All guidelines used in the division are available under downloads
Applications for registration of conventional medicines involve the submission of a completed application form together with a dossier of supporting documents in the Common Technical Document (CTD) format. The process has been summarised in the steps below.
Step One: Application Requirements
The process of registering a conventional medicine requires the completion of the statutory application form MC-8. Dossiers should be completed in accordance with the MCAZ CTD Guidelines which provide guidance on supporting information required and presentation format of the application dossiers. This guidance document is essential for first time and seasoned applicants to ensure good quality applications are submitted. Applications for generic solid dosage forms (tablets, capsules, suspension etc) medicines may require the submission of a bioequivalence study, and additional guidelines are available for use by the applicant.
Step Two: Payment Procedure
The application fees for conventional medicines are stipulated in the statutory fee schedule. There are three main types of medicine applications that attract different application fees. These are:
The applicant completes the EVR Quotation Confirmation Form and submits to the Evaluations & Registration Division using the following email This email address is being protected from spambots. You need JavaScript enabled to view it.. The division staff will complete the form and send it back to the client with appropriate fees for the service required. This is to ensure that the appropriate payment for the application is quoted and paid to the Authority. When payment has been received successfully by the Medicines Control Authority of Zimbabwe (MCAZ) i.e evidence of payment presented, an MCAZ receipt is issued. A specific job invoice will then be generated by the MCAZ Finance division using a completed and signed EVR Quotation Confirmation Form and only then can an application for registration of a medicine be submitted.
Step Three: Submission Process
New applications can be submitted from 8.00 am to 4:30 pm Monday to Friday. The receiving officer will only accept a submission if payment for the application has been made. The applicant is required to provide the following when submitting an application for registration:
The application will then be screened for completeness using the appropriate screening checklist depending on whether the product is a small molecule or biological and a response of the outcome of the screening will be sent to the client within 90 days of receipt.
Passed Screening
Applications that pass screening will progress to the evaluation stage. Communication to this effect will be sent within the stipulated 90 day period.
Failed Screening
In the event that an application is incomplete and fails the screening stage, the applicant can re-submit a complete application at a later date. This re-submission will incur a $600 excl. VAT resubmission fee. The quotation form will be sent together with the communication that the product has failed screening.
Registration Timeline
Complete applications that contain all the required technical and administration information ordinarily get registered after 1 or 2 review cycles. Incomplete applications with deficient information are the ones that usually need 2 or more review cycles including time for representations thus the total time to registration is longer for such applications.
Status Update
For a status update on the submitted applications, the applicant is required to fill in the status update form and send it to This email address is being protected from spambots. You need JavaScript enabled to view it..
Click the here to download the forms
Applications for registration of veterinary medicines involve the submission of a completed application form, together with a dossier of supporting documents in the CTD format. The process has been summarised in the steps below.
Step One: Application Requirements
The process of registering a veterinary medicine requires the completion of the statutory application form MC-8. Dossiers should be completed in accordance with the veterinary medicines guidelines which provide guidance on supporting information required and presentation format of the application dossiers. This guidance document is essential for first time and seasoned applicants to ensure good quality applications are submitted. Veterinary vaccine guidelines must be consulted when preparing applications for registration of veterinary medicines.
Step Two: Payment Procedure
The application fees for veterinary medicines are stipulated in the statutory fee schedule. There are three main types of medicine applications that attract different application fees. These are:
The applicant completes an EVR Quotation Confirmation Form and submits to the Evaluations & Registration Division using the following email This email address is being protected from spambots. You need JavaScript enabled to view it.. The division staff will complete the form and send it back to the client with the appropriate fees for the service required. This is to ensure that the appropriate payment for the application is quoted and paid to the Authority. When payment has successfully been received by the Medicines Control Authority of Zimbabwe (MCAZ), an MCAZ receipt is issued. A specific job invoice will then be generated using the EVR Quotation Confirmation Form and only then can an application be submitted.
Step Three: Submission Process
Application submission is open Monday to Friday from 8am to 4:30 pm. The receiving officer will only accept a submission if payment for the application has been submitted. The applicant is required to provide the following when submitting an application for registration:
The application will then be screened for completeness using the screening checklist and a response of the outcome of the screening will be sent to the client within 90 days of receipt.
Passed Screening
Applications that pass screening will progress to the evaluation stage. Communication to this effect will be sent within the stipulated 90 day period.
Failed Pre-Screening
In the event that an application is incomplete and fails the screening stage, the applicant can re-submit a complete application at a later date. This re-submission will incur a $600 excl. VAT resubmission fee.
Registration Timeline
Complete applications that contain all the required technical and administration information ordinarily get registered after 1 or 2 review cycles. Incomplete applications with deficient information are the ones that usually need 2 or more review cycles including time for representations thus the total time to registration is longer for such products.
In September 2015 a statutory instrument S.I. 97 of 2015 was enacted mandating the approval of complementary medicines. Complementary medicines are usually used in conjunction with conventional therapy in humans with the aim of improving the disease condition or general wellbeing of the person or animal. Applications for approval of complementary medicines involve the submission of a completed application form together with a dossier of supporting documents in an acceptable format. The process has been summarised in the steps below.
Step One: Application Requirements
The process for approval of a complementary medicine requires the completion of the statutory application form CM-1. Dossiers should be completed in accordance with the Complementary Medicines Guidelines which provides guidance on supporting information required and the presentation format of application dossiers. This guidance document is essential for first time and seasoned applicants to ensure good quality applications are submitted.
Step Two: Payment Procedure
The application fees for complementary medicines are stipulated in the statutory fee schedule. The cost per complementary medicine application is $600 excl. VAT.
The applicant completes an EVR Quotation Confirmation Form and submits to the Evaluations & Registration Division using the following email This email address is being protected from spambots. You need JavaScript enabled to view it.. The division staff will complete the form and send it back to the client with the appropriate fees for the service required. This is to ensure that the appropriate payment for the application is quoted and paid to the Authority. When payment has successfully been received by the Medicines Control Authority of Zimbabwe (MCAZ), an MCAZ receipt is issued. A specific job invoice will then be generated using the EVR Quotation Confirmation Form and only then can an application be submitted.
Step Three: Submission Process
Application submission is open Monday to Friday from 8am to 4:30 pm. The receiving officer will only accept a submission if payment for the application has been submitted. The applicant is required to provide:
Approval Timeline
Complete applications that contain all the required technical and administration information ordinarily get registered after 1 or 2 review cycles. Incomplete applications with deficient information are the ones that usually need 2 or more review cycles including time for representations thus the total time to registration is longer for such products.
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