We enjoy a clear understanding of the regulatory environment in South Africa, its history, trends, current requirements and policies. We are associate members of many of the industry associations and in our professional capacities affiliated to the professional associations. These associations, together with networks we have nurtured, provide us with current information related to the health products industry and medical devices.

Our aim is to provide exemplary quality regulatory support, thereby reducing unnecessary delays in the registration process.

We use the most up to date solutions to enable us to compile and publish eCTDs i.e. Freyr eCTD systems. We are able to life cycle manage documentation, thus maintaining registration documents in a fully validated electronic document management system.
We aim to empower our customers with the knowledge and understanding of the regulatory environment and processes. This is vital to our clients to understand the regulatory environment related to the industry and enables them to make informed decisions regarding their products.

Our services range from regulatory assistance with medical devices, orthodox medicines to complementary medicines, from veterinary medicines to licensing of facilities. We can answer all your questions and fulfil all your regulatory requirements!