At Evohealth, we manufacture according to GMP as per standards set out by SAHPRA/MCC and other regulatory authorities such as WHO (World Health Organization – Geneva) or USFDA (United States Food and Drug Association) and PIC’s.
More than 40 years of experience
We are passionate about people and strive to educate communities on creating a healthy life and improved well-being. This drives us to offer affordable, alternative formulae with enhanced health benefits for our customers.
Evohealth specialises in licensing, manufacturing, registering, marketing and distributing affordable pharmaceutical medication and medical devices, which includes developing and providing turnkey, end-to-end solutions to meet the specific requirements of our clients.
To provide healthcare products and services of the highest quality, safety, efficacy and affordability.
To be the most progressive South African pharmaceutical company by 2023.
Our Ethos & Processes
To provide high quality medication and medical devices, we ensure that all our suppliers adhere to GMP (Good Manufacturing Practice).
In an effort to lower the cost of quality medication, medical devices and healthcare services for both public and private sectors, we adapt to the dynamic, progressive pharmaceutical industry trends and developments. Our medical devices carry international accreditations, which include CE Marking and ISO13485. Our aim is to change the healthcare landscape by making available new innovative products that improve the quality of life for all patients and the community at large.
Our Quality Control
We are ISO9001:2015 certified. Our Quality Management System takes into account all vital aspects as to how the company is managed and how people understand their role in the organisation. Our efficient and cost-effective structure contributes to quality products and services, which effectively results in an improved patient well-being.
Our Quality Standards sets the benchmark for a harmonised model in our pharmaceutical quality system throughout the lifecycle of a product and is intended to be used together with regional GMP requirements.