What is the meaning of "regulatory convergence"?

The term "regulatory convergence" refers to the process in which regulatory authorities move towards standardizing their practices, particularly in the context of international trade. This is crucial for ensuring that products, including medical devices, can be traded across borders with minimal barriers, while still maintaining safety and efficacy standards. By harmonizing regulations, countries can enhance mutual recognition of each other's regulatory frameworks, facilitate smoother market entry for manufacturers, and ultimately promote public health without compromising safety.

This process helps to reduce differences in regulatory requirements that can create obstacles for companies wishing to market their products in multiple countries. As a result, regulatory convergence contributes to global trade efficiency and ensures that innovations are quickly and safely brought to markets worldwide.