WHO GMP Guidelines (Good Manufacturing Practices) define the minimum requirements pharmaceutical manufacturers must meet to ensure products are consistently high in quality. These guidelines cover critical aspects like hygiene, controlled environments, validated processes, and staff training. In 2025, compliance with WHO GMP Guidelines is essential for manufacturers aiming for international recognition and regulatory approval. These standards not only enhance product safety but also streamline production efficiency and global market access.
The pharmaceutical industry plays a critical role in global health, and the World Health Organization (WHO) ensures that this role is governed by international standards that prioritize safety, efficacy, and quality. In 2025, adherence to WHO guidelines in the pharmaceutical…
