Market Authorisation

Market authorization is an official process whereby a government or regulatory body approves a new product, such as a medicine or medical device, for sale and use within their jurisdiction. It involves a thorough evaluation of the product’s safety, effectiveness, and quality based on scientific evidence. Once granted, it allows the manufacturer to legally distribute the product to consumers. This process helps ensure that products meet standards to protect public health, and it is vital for bringing innovative treatments and technologies safely to market.