Regulatory
affairs
Regulatory surroundings are compelling and complex nowadays that licensing applications for products in the Saudi food and drug government agency sometimes fail to receive approval from the first time and takes a lot of time.
Companies are required to have essential knowledge and requirements of all Saudi FDA regulations before proceeding for their business expansion in Saudi Arabia.
The probability cost of these failures is in millions. This is why we’re here to help and guide you over the difficulty and complex process of registering a product in the Saudi FDA.
SuLinda has its own Regulatory Affairs department to offer regulatory support for Pharmaceutical and healthcare company’s field. We offer regulatory submission services related to Food, Cosmetics, herbal, medical Devices and drug Products in Pharmaceutical Companies.