Since all pharmaceutical products aim at health recovery, three factors must be highlighted as crucial watch points during the manufacturing process: safety, bioavailability and stability.
To secure international standards in a pharmaceutical product, it is inevitable that the formulation, mixing, batch preparation , filling and packaging of all products be done automatically with no dependence on manual handling. Adopting the cGMP guidelines and watching the often-made managerial quote “BOX IN A BOX”, each Farabi manufacturing process has its own special space and corresponding production line. In this way, products are protected against any contamination which might occur as the result of a shared interior manufacturing space. Different sections thus defined and specified are equipped with their own air-filtering systems. Advanced machinery facilitates the automatic handling of raw materials through the subsequent processes of formulation, mixing, batch preparation, filling and packaging. Another highlight of Farabi’s technological competence is its capability to convert fine powder to compact powder. As we know, it is an advantage for providing the medical powder with good distribution of particle size, good flow and higher chemical and physical stability.
This method is very useful and profitable for those compounds that are not stable in humidity or those compounds that are susceptible to hydrolysis.
Finally, Farabi Pharmaceutical Complex has been designed for the 21st century.

The first duty for any pharmaceutical manufacturing company is to be sure of maximum safety of its patients and its drugs effectiveness. To reach this guaranteed quality for Farabi products, different on-site laboratories work together such that quality control is found to be stringent at every stage of manufacturing in Farabi Complex. These laboratories are staffed with highly trained personnel who enjoy the academic as well as the experimental expertise required for performing the often-complex evaluation analysis. Quality control is maintained at FarabiComplex by observing unanimously approved international standards as well as the latest guidelines set by FDA. These checks cover all manufacturing steps, starting from the very act of purchasing the raw materials down to the culminating phase of packaging, storage and distribution. All in all, Farabi’s research panel including pharmacists, chemists, microbiologists, engineers and technicians have one aim: QUALITY.
Meanwhile, the results of bioequivalency and bioavailability studies have proved that Farabi quality control team’s efforts have not gone to void, as Farabi Pharmaceutical Complex has been honored the business initiative directions Gold Star Award for Quality in 1997.

There is always the need to emphasize that all pharmaceutical manufacturing centers strive to Prolong human life and this by necessity obliges them not to pollute nature or threaten organic life. Farabi Pharmaceutical Complex cares about soil, air and water as the essences of life.
Hence, it is expectable that Farabi would design and develop its own water recycling system to treat all human and industrial waste water by implementing chemical and biological methods.
The result is of course favorable and prevents the polluted water from contaminating soil, air and underground water resources exterior to the production site. Consequently, the recycled water is used for watering the green area.
As for the air-filtering systems, Farabi observes the guidelines of cGMP regarding Roll-O-Maticand Electro Static filters to absorb particles in the air and to prevent the scattering of the antibiotic powder through the let-out air.
Farabi’s congeniality with nature and the environment has not only brought about product quality promotion but also attracted the favorable attention of Iranian Organization for the Preservation of Environment which named and nominated Farabi Pharmaceutical Complex as the winner of the prestigious titular certificate The Green Industry” of the year, in 1999.