science
BR Consultation Gaborone, Botswana

question_answer Frequently asked questions

chevron_right What regulatory areas does BR Consultation cover?
We provide structured support across Good Manufacturing Practice (GMP) compliance, cosmetics regulatory alignment, complementary medicines registration, chemicals classification and labelling under the Globally Harmonized System (GHS), and science project management. Our Consultancy is fully based on Botswana and SADC requirements.
chevron_right Do you assist with product registration in Botswana?
Yes, we provide full support for product registration in Botswana, including technical dossier compilation, safety assessments, regulatory documentation review, and liaise with Botswana Medicines Regulatory Authority (BoMRA) and local bodies for cosmetics and complementary medicines.
chevron_right What does “manufacturer details” mean in your form?
If you already have a contract manufacturer, share their name, location, and certifications. If not, we can recommend vetted GMP-compliant partners in southern Africa.
chevron_right Are you limited to companies in Botswana?
Primarily we serve Botswana-based companies, but we also consult for international businesses seeking compliance in Botswana and SADC. Gaborone is our home.