The quality control department at SPB Pharma is involved in testing of each and every raw material and packaging material entering the premises. On receipt of goods receipt from stores, the sampling testing is done as per written specifications.

Microbiological testing is done of raw materials, water, air, contact parts of machine, and finished goods as appropriate.

The Q.C. department is responsible for in-process Quality control activities, finished product analysis and analysis of validation samples.

Batch documents are prepared, and issued by a technically competent person from the Q.C. dept. for each planned batch. On completion of the batch, all the filled documents (BMR) are sent to Q.C; along with all relevant records.

The Q.C. department also plays an active role in preparation and finalization of MFR's training, audits, validation, etc.

Thus, the Q.C. dept. exercises its control from the start of any manufacturing process till the end of it.

All these augment our position as a leading generic drugs manufacturer in India.

Our Labs

SPB Pharma is a generic drugs manufacturer that has stringent quality control norms. By and large, we have a full-fledged analytical laboratory, which caters to most of our needs.

For certain tests requiring highly sophisticated instrumentation, we employ the services of reputed and duly approved analytical testing laboratory, with due intimation to FDA, Simla. Making us one of the most respected drug manufacturer and pharmaceutical exporter in India.