From engineers to designers, researchers to strategists, our diverse team is united by a shared commitment to improving healthcare and making a positive impact on the lives of patients. Get to know the faces and stories behind our groundbreaking work as we strive to reshape the future of medical devices and deliver impact at scale.
Empowering lives though accessible healthcare innovations and medical technologies.
We are driven by the belief that everyone deserves access to quality healthcare, and we are committed to finding innovative solutions that address this pressing need.
Striving to improve the lives of millions of people around the world by pushing technological boundaries.
We develop high-quality, affordable MedTech products and healthcare solutions that impact human suffering on an individual and global scale.
Committed to empowering at least 250 million people with life-saving medical innovations.
Impulse Biomedical aspires to become the largest and most trusted African medical devices company, with a leading global reputation and footprint
We exist to make people’s’ lives better by easing access to healthcare. The needs of the people is what excites us and drives our actions.
The stakes are high and so are our engineering standards which output novel, carefully-designed medical devices.
We proudly utilise our natural resources sustainably, to solve local problems with a cost-effective approach.
Obtaining License and Regulatory Approval: Ensuring Compliance for ZiBiPen.
Impulse Biomedical has obtained a manufacturing licence from the South African Health Products Regulatory Authority (SAHPRA). As a licence holder Impulse is authorised to perform manufacturing activities (Manufacturing, Distributing, Importing and Exporting) for our listed medical devices that comply with the Medicines and Related Substances Act and all relevant SAHPRA guidelines.
Impulse Biomedical is undergoing ISO 13485 certification ensuring that all our medical devices consistently meet customer and applicable regulatory requirements . Integral to our quality management system (QMS) is a risk management process, in line with applicable medical device standards, to identify, estimate, evaluate and control risks associated with our medical devices.
