In the past, discrepancies between manufacturing and sales approvals and actual manufacturing practices at manufacturing sites have been identified in the pharmaceutical industry.
As a result, there is an even greater need to strengthen compliance in quality assurance operations within the manufacturing and sales industry, with the Ministry of Health, Labour and Welfare issuing an order in April of this year to "conduct inspections to ensure consistency between manufacturing and sales approval certificates for generic drugs and the actual manufacturing and testing methods."
In addition, the domestic labor market is experiencing a shortage of supply, making it difficult to secure sufficient time and manpower for quality assurance work.
To solve these problems, we have released a manufacturing and sales approval checker service that uses AI to streamline document matching and inspection work.
In this seminar, we will introduce the environmental changes occurring in the pharmaceutical industry, the challenges they pose, and solutions to these challenges, with demonstrations.