Harmonizing pharmaceutical legislation

Description

Harmonizing pharmaceutical legislation involves aligning national laws, regulations, and standards governing medicines to ensure consistent quality, safety, and efficacy across borders. This strategy addresses problems such as regulatory fragmentation, barriers to trade, and unequal access to essential medicines. By streamlining approval processes, facilitating mutual recognition, and promoting international cooperation, harmonization reduces duplication, accelerates access to new treatments, and strengthens public health protections globally.