To Train, Develop and Motivate all the staff members to follow the pre-determined written procedures and maintain records of compliance of GMP & GLP as enshrined in the constitution of the Corporate Quality Manual.

To observe GMP by adhering to, well defined manufacturing processes, with proper in-process control and necessary requirements such as personnel, premises, plant and validated procedures.

To observe GMP by adhering to, well defined manufacturing processes, with proper in-process control and necessary requirements such as personnel, premises, plant and validated procedures.

To observe good housekeeping and to maintain the building and precincts in hygienic conditions by adhering to the written cleaning and waste disposal procedures.

To retain a well equipped maintenance team, with laid down procedures for preventive and break down maintenance.

To strictly adhere to the written specifications, of all raw materials and packaging materials, laid down by a committee comprising of quality assurance manager, production manager, purchase manager, marketing manager, finance manager and approved by the management subject to periodic reviews. Special storage conditions to be laid down where required.

To exercise and maintain efficient control over all the processing activities in accordance with the written instructions (process SOPs) and maintain a systems mechanism of production records, to facilitate an easy and complete tracing of each discreet lot of products back to the identity of the starting materials / intermediates. Any abnormality or deviation from the desired critical parameters are recorded and are the subject of an investigation. To observe validated cleaning procedures to ensure thorough cleaning of equipment between processes.