Almadany Pharma

Regulatory Affairs Department:

latory Affairs

The Registration Department prepares the information and files necessary for the registration process in coordination with the sales departments and supplier companies, prepares files and the necessary information on new items, conducts the registration process for them with the competent authorities, communicates with the supplier companies to obtain all the necessary information for this, and follows up the registration process with the Supreme Authority For medicines and the Ministry of Health until its completion.


The department follows up on the quality of pharmaceutical products after marketing, by capturing and evaluating side effects and developing solutions that lead to their prevention, receiving reports related to any side effects of medicines or problems related to the use of medicine, following up on news received from international bodies and organizations and taking the necessary action in a timely manner in coordination with the related authorities and partners.