Pharmacovigilance is regulated by a set of international standards that define common rules for all market participants. Key documents include ICH E2 guidelines, the European GVP (Good Pharmacovigilance Practices), and the requirements of...
In a pharmaceutical laboratory, there are no secondary tasks. Every analysis influences product safety, quality stability, and the predictability of supply. This is why training new employees is not a formality but...
Quality consistency is the laboratory’s ability to produce the same results when testing every new batch of a substance. For example, if purity remains steadily at 98%+, without fluctuations like 97–96–99–95%, this...