Home 5

We adhere to the practical application of all the procedures required to register pharmaceutical products as well as comparing locally registered pharmaceutical products to the imported ones. We also carry out studies of stability, bio-availability, dissolution … etc. in certified entities known for their efficiency on the local and international levels.

We adhere to the highest international standards of manufacture starting from the import of raw materials from reputable reference countries and factories that hold Good Manufacturing Practice (GMP) certificate, proceeding to manufacturing and packaging in accordance with regulations of the Food and Drug Administration (FDA), provided that the name of our company or the pharmaceutical product is written on each tablet as well as on the strip in a manner that cannot be imitated.

We only distribute our pharmaceutical products through authorized distributors who adhere to all the regulations established by ministries of health in their countries; where pharmaceutical products are stored in well-aired places, appropriate areas, freezing chambers and equipped vehicles for distribution of medicine as well as an automatic system that allows the printing of patch number, expiry date …etc.

We are committed to prepare our promotional materials on scientific basis and in compliance with the medical fields under which the pharmaceutical product was registered, either in the reputable reference countries or the countries where we work accurately, also we provide our medical representatives with the required training to enable them to perform their jobs effectively.