Quality in MUP is clearly established at all phases of the product life cycle. Quality supervision begins at the examination facilities with careful documentation and general conduct of non-clinical safety studies. This ensures compliance with current Good Laboratory Practice (GLP) and consequently, the integrity of the data produced. Once a product gains regulatory approval and enters routine manufacturing, quality is guaranteed throughout the process, for both drug substances and drug products.

The Quality Control Department supervises and monitors the adequacy of conditions under which raw materials, semi-finished products and finished products are stored. Hence, the manufactured products released for sale are of the highest standard.