Frequently Asked Questions

FAQs

We’ve compiled answers to some of the most common questions about our services, processes and regulatory consulting expertise. Whether you are new to the industry or seeking clarity on specific requirements, this section is designed to help you find quick, reliable information.

Still have questions? Feel free to reach out — we are here to help.
How does costing work?

Our consulting services are offered based on an hourly rate; however, as each product and company is unique, each project is quoted individually based on the scope thereof.

What are the project timelines?

Timelines are subject to the quality of information received and the level of difficulty involved and will be unique to each project. We strive to always deliver prompt, effective and high-quality services.

Where are you located?

We currently have three offices, located in Potchefstroom (North West Province), Centurion (Gauteng) and Cape Town (Western Cape). We also maintain a virtual presence and are available to meet with you at your convenience.

In which markets do you work?

South Africa, SADC and Sub-Saharan English-speaking countries and we collaborate with various global partners around the world.

Do you register medicines?

We are the consultants facilitating the process of your product registration and can assist you with the registration process and requirements for the respective regulatory authorities.