We observe strict quality control at each and every phase of production, from selecting the raw material to the stage of packing, storage and forwarding. Every activity is closely monitored by efficient and responsible staff. The company has valid GMP certification & ISO 9001:2008 that authenticates the quality compliance of the products.

SAS strictly follows the GMP norms. The basic premise on which its R&D facility functions, are as follow: Authenticity and quality of raw materials, Manufacturing standards as per GMP norms, Quality Control of the manufactured drug, Lot of emphasis on hygiene, state-of-the-art equipments and documentation etc.

As per the Global GMP norms, SAS is continuously improving its facilities and working, specially at the level of: Raw Materials, Excipients, Packing Material, Intermediate Product, Finished Products, its Stability and Micro-biological Testing.

The in-house R&D is equipped with all the major instruments and analytical equipments required to undertake the following testing and analysis at different stages of production.

Raw Materials: Raw material analysis, Identification of foreign material, Extractive value of water and extractive Alcohol Soluble ingredients, Ash Values, Acid insoluble Ash content, Estimation of Volatile Oil and PH value, Moisture Content, Micro-biological Testing.

Finished Products: Uniformity of the weight of the Capsule, Total Ash content, Acid insoluble Ash, Alcohol and water extractive value, Disintegration time of the Capsule, Micro-biological, Toxicology & Safety Data testing is also done for finished products.

Our R&D is fully equipped with the latest equipment like Incubator, Autoclave, TLC Kit, Oven, Bulk density, Muffle Furnace, Moisture Balance, PH meter and B.O.D. to name of few.