Quality assurance is a major challenge, particularly in light of growing regulatory stringency and the international dimensions of trade, rightly so, since manufacturing of substandard medicines result in prolonged treatment for patients, drug resistance and increased incidence of adverse effects.

We at Gag follow the self-implied stringent quality standards to ensure that all the products being manufactured are consistently safe, effective and of good quality.

While the general principles of GMP apply for all types of pharmaceutical products.

At Gag, we take pride in stringent following of specially developed protocols for hygiene, sanitation and processing that are specific to herbal products. Some of these are:

• Storage facilities with quarantining of incoming herbal matter to prevent the spread of microorganisms.

• Maintenance of segregated areas for different materials and of appropriate environmental conditions.

• Production areas controlled for dust, fumes and vapors generated by the processing of these substances.

• Cleanliness of equipment to avoid microbiological contamination as per US FDA GMP norms.

At Gag, we ensure that each major stage of the manufacturing process is validated to ascertain that the finished products
comply with all quality and design protocols, and consistently meet their specifications. In other words, we ensure that quality; safety and efficacy are designed and built into our products.