Quality is customer driven and not merely a departmental obligation. It is significant to everything and everyone in the organization. To ensure Total Quality Management, the Quality Assurance (QA) department in our factory is autonomous in its functioning. In-house quality checks, which are detailed in our Standard Operating Procedures (SOP), have been drawn up in addition to the recommendations specified in the US, British & Indian Pharmacopoeias for each of our operations commencing from the raw material audit to in-process checks through finished product inspection.

Raw materials are accepted for manufacturing only after it is found to be of respective pharmacoepial grade by our in-house and independent laboratories. Finally we reiterate our commitment to quality and strive to produce a zero defect product.

Quality is customer driven and not merely a departmental obligation. It is significant to everything and everyone in the organization. To ensure Total Quality Management, the Quality Assurance (QA) department in our factory is autonomous in its functioning. In-house quality checks, which are detailed in our Standard Operating Procedures (SOP), have been drawn up in addition to the recommendations specified in the US, British & Indian Pharmacopoeias for each of our operations commencing from the raw material audit to in-process checks through finished product inspection.

Raw materials are accepted for manufacturing only after it is found to be of respective pharmacoepial grade by our in-house and independent laboratories. Finally we reiterate our commitment to quality and strive to produce a zero defect product.

Quality is customer driven and not merely a departmental obligation. It is significant to everything and everyone in the organization. To ensure Total Quality Management, the Quality Assurance (QA) department in our factory is autonomous in its functioning. In-house quality checks, which are detailed in our Standard Operating Procedures (SOP), have been drawn up in addition to the recommendations specified in the US, British & Indian Pharmacopoeias for each of our operations commencing from the raw material audit to in-process checks through finished product inspection.

Raw materials are accepted for manufacturing only after it is found to be of respective pharmacoepial grade by our in-house and independent laboratories. Finally we reiterate our commitment to quality and strive to produce a zero defect product.