All Pharmaceutical Industry aims to make products with good quality products so this can be done by allowing In-Process Quality Control (IPQC) Approaches. The importance of IPQC to carry out complete testing before, after and during the manufacturing process is completed for the Products or to Monitor and improve effectively the whole applied process at the every stage of the finished pharmaceutical products by according to Standard Operating Procedures (SOPs). This article proposes to establish clearly written in-process methods for critical points at all stages of the product their documentation and review.