Following the industry meeting between SAHPRA (Medicines Regulatory Board of South Africa) and the Industry CEOs which MnandiPharma was present at, we can summarise the motion as a positive and supportive towards the newly founded companies in the industry as well as accommodative for the current businesses. Continue reading “Medical Device Industry meeting – SAHPRA & Industry CEOs”
We are very pleased to introduce our Medical Device Classification module guide to welcome new parties into the industry and help them understand how devices are classified. MnandiPharma prides itself in pushing boundaries of previously unanswered norms of the industry, just as the regulation itself breaks away from the Medicines regulations.
Please feel free to try it out as many times as you please, however, we do disclaim that it is purely for educational purposes and does not claim to stand any authority whatsoever. The module is based purely on the guidelines.