A dedicated team to ensure that the drugs manufactured are in strong compliance to the GMP as per WHO guideline standards has been crafted. Review of documents, revision of validation procedures, upgrading analytical procedures, monitoring protocols, sampling surveillance, product wise review on monthly basis and master formula maintenance is carried out by the team headed under the guidance of eminent professionals both from within the highly qualified staff at the unit and other organizations comprising of consultancy firms and quality management systems providers. Involvement of educational institutions and researchers has also proven to be beneficial in the quality process of the company.

The environment of the firm is absolutely free from all type of contamination. No toxic or hazardous substances are processed or evolved during the process. SOP drives all the activities carried at the unit and are strictly adhered to under constant intendance of highly qualified personnel.

Quality wing of the factory has been provided with control systems to ensure zero contamination. To certify the product is of highest standards Rhydburg Pharmaceuticals has analogous parallel operation with laboratories recognized from the Government of India.

Specifications and Standard Testing Procedures are prepared by Quality Control and finally reviewed and issued by Quality Assurance department. In case of regulatory specifications and testing protocols, Department of Regulatory Affairs is consulted. Quality Control & Quality Assurance are both supervised by approved and experienced staff directly reporting to the management but independent of the other departments. Apart from the quality control and quality assurance team a specialized and independently functioning team of quality management is operational headed by the technical director in close consultation with the Managing Director which constantly gazes the entire processes and activities carried out in the premises. Audit and approval of vendors and contract manufacturers, evaluating and analyzing market complaints and batch recalls are investigated by the quality team and nullified to negligible in the past years.

The total Quality Management System is designed for ‘Zero Defect Product’ for which the Quality Assurance Executive is responsible. The unit has its own fully equipped laboratory with almost all the In-House testing facilities of the products being manufactured.