Published Paper Details:

A company's force as well as its character largely depends on whether there are complaints about the company's marketable products. Any disfigurement in the injectables can beget serious diminishment to the manufacturing company which has a good character up to now. Once the injectables placed in the request, post-marketing surveillance is an important factor in controlling its adverse goods on the population. The source of the claim can be anything, i.e., shipping, manufacturing and packaging, labeling, breakage of vials, etc. Any error in any of this way can lead to serious problems. thus, dealing with request complaints should be a major task. This critical step requires a single, unified and secure platform for managing product complaints from launch to finish. Request complaints are thus prioritized according to easily defined procedures. In the event of a serious complaint, a root cause analysis should be conducted to resolve the issue and similar injectable products should be removed from the request. The recall system must be so effective that the product can be removed from the request within a specified period of time. The study outlines the typical process for resolving request complaints and product recalls from FDA authorized officer.[1]