Ointments and Liquid Orals - SUYOG PHARMACEUTICALS PVT. LTD.

Commitment to Quality

The Quality Control Department contains all the facilities necessary to analyse both, the raw materials and the finished products. Currently, the plant operates under the standard operating procedures for good manufacturing practices, good laboratory practices, good storage practices, system validation, water system validation, documentation and record maintenance, commensurate with National and
International regulatory requirements.

There are two water purification systems installed at the factory – purification by a deionisation system with a capacity of 66 litres/hour; and purification by distillation, with a storage capacity of 225 litres. The plant has all the requisite facilities for conducting analytical tests at different production stages, to ensure the safety, identity and efficacy of the product line. There is also a modern microbiology
division that is responsible for the detection of microbes in every product manufactured at the plant.

The factory strictly adheres to the IPQC (In Process Quality Control) methodology. Without IPQC supervision, no weighing, manufacturing, filling or packing operation is permitted, and line clearance for all these operations is mandatory. The factory is completely fumigated every evening, and during the day, antiseptic sprays are used during the break intervals, in order to minimise contamination levels.

Suyog Pharmaceuticals has obtained all the necessary licenses of drugs falling under Schedule C & C1, and other licenses pertaining to the Central Excise Factory and Pollution Acts. Assistance from approved Public Testing Laboratories for testing of raw materials and finished products that sometimes require specific sophisticated tests like G.C. and I.R. is obtained, to further ensure quality control at the plant.