Production Platforms

MUP manufactures 130 products. MUP manufacturing line encompasses;
  • Semisolid form: ointments cream and gel.
  • Liquid fills: syrups, suspension and solution.
  • Sterile product: ampoules and vials.
  • Solid form: tablets, capsules, suppository and powder.


We are building sustainable assets for our business by opening our new factories (Penicillin and Cephalosporin by June 2013) and starting from this date we will be considered as one of the top pharmaceutical manufacturing companies in the MENA regions
Persistent dedication to these objectives MUP acquires the latest version of ISO 9001 and working on obtaining ISO 14001


Our MUP warehouse management system coordinates material flow using a database driven computer program after passing the fully equipped sample room where materials are accurately examined.


MUP acquired ISO 9001:2008 certified and is upgrading the plants to be certified to (ISO, 14001, 18001 & 17025) by the end of year 2015 .planning to get accreditations of ISO 14001:2004 and ISO 18000:2007 Quality in MUP is clearly established at all phases of the product lifecycle. Quality supervision begins at the examination facilities with careful documentation. 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. During production:

• Manufacturing processes are validated and equipment is tested and certified. 

• Test methods are confirmed to ensure that each product is of reproducible quality. 

• Continuous improvement practices are employed so that processes and procedures are continually updated.


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