Registration of pharmaceutical products and factories
We register pharmaceutical products and factories as quickly as possible.
Depending on Sfda requirements and GMP standards This process requires providing accurate information about drugs and medical products to health authorities in the country.
This process includes submitting details about the composition of the products, manufacturing methods, clinical trials, and potential side effects.
The goal is to ensure the safety and efficacy of the products before they enter the market, in addition to regulating the factories that produce them to ensure compliance with health standards.