Our Procedure

As soon as any batch has been finally packed, the in-process Q.A. personnel draw random samples of the finished goods. These random samples are tested against approved specifications by the Q.C. department. These specifications are normally more stringent than the pharmacopoeia requirements. If the random samples meet the specifications, the Quality Control department certifies that the goods meet the laid down specifications.
The batch production record is then reviewed by the Quality Assurance Manager. He checks for the completeness of the documents and for the compliance with c-GMPs at various steps. The Q A Manager releases the batch for distribution by signing the BPR.
We have established well equipped Quality Control Lab. QC Lab has been divided into three wings :
Chemical Laboratory. Instrumental Laboratory & Microbiological Laboratory. Beside QC, we have IPQC lab for Beta Lactum as well.