What Is The Regulatory Framework For Drug Quality Audits In Japan?

In Japan, drug quality audits are governed by the Pharmaceuticals and Medical Devices Act (PMD Act). The Ministry of Health, Labour and Welfare (MHLW) and the Pharmaceuticals and Medical Devices Agency (PMDA) oversee compliance, ensuring Good Manufacturing Practice (GMP) standards are met to ensure safety, efficacy, and quality of pharmaceuticals.

Leave a Reply

You must be logged in to post a comment.