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Medisynth Blog



This is a process through which a business seeks to ensure that product quality is maintained or improved and manufacturing errors are reduced or eliminated. At Medisynth, we have separate IPQA and IPQC departments to control quality. They are responsible for testing of herbs and other raw materials for their pharmacopoeial, that is, drug-making requirements. We carry out tests like Thin Layer chromatography and UV Spectrophotometer to determine the purity of the herb. Medisynth’ s consistency and reliability in operations are at par with global standards in the industry.



Medisynth follows stringent standards of current Good Manufacturing Practice (cGMP) in homoeopathy and has a cGMP certified manufacturing facility. Our systems are well documented and implemented by a team of trained and efficient staff. Manufacturing takes place under the supervision of expert technical personnel. A separate building premise is dedicated for the preparation of Mother Tinctures & Dilutions. The area is fitted with explosion resistant and flameproof fittings to avoid any accidents. We follow European (EU) standards for fumigation of pharmaceutical areas to maintain the highest quality of hygiene. There is a dedicated AHU (Air Handling Unit) in every manufacturing section to avoid cross-contamination and also to maintain ideal humidity, temperature levels and air purification. Every product we manufacture and distribute meets with and conforms to internationally accepted standards of quality, purity, efficacy and safety.