Product Evaluation and Registration
Processes
1. Registration Process
Summary of the Registration Process:
Submission of Dossier:
The applicant submits a comprehensive dossier containing all required information, including data on the product's safety, efficacy, and quality.
Scientific Assessment:
The dossier undergoes a rigorous scientific assessment to evaluate the product’s safety, efficacy, and quality against established criteria.
Granting of Marketing Authorization (MA):
Products that meet the regulatory requirements are granted Marketing Authorization (MA) or Registration, allowing them to be marketed.
National Register:
Once approved, the product is added to the national register, ensuring transparency and accessibility of information on authorized products.
Validity and Renewal:
The marketing authorization is valid for a specified period (e.g., 5 years) and must be renewed for continued market access.

Process Automation

2. Exemption Process
Exemption from registration – a process in place to facilitate access to good quality medicines/ medical devices which are not registered and/or where registered alternatives are not available in Botswana
Exemption
- 1. Application form
- 2. Proof of payment
- 3. Recent Certificate of Analysis
- 4. Current Good Manufacturing Practice Certificates
Review
- 1. Check the completeness of the application (supporting documents according to type) and if there is a registered alternative
- 2. Make necessary recommendations.
- 3. approval