The Decree that regulates the requirements for authorization to introduce health products, herbal and homeopathic medicines for human use on the market was recently published, with the aim of guiding those responsible for research, manufacture, import, distribution and export and sale to retailers and other interested parties on the conditions to be met in order to obtain a Marketing Authorization (“AIM”) in line with the provisions of Law No. 12/2017, of September 8 and with the WHO and the guidelines of SADC countries, with a view to ensuring that products marketed in the country do not cause public health problems.