Snapshot

The Simplified Registration Procedure pathway has been developed by the Medicines and Medical Devices Agency (MMDA) of Moldova.

This pathway accelerates the regulatory review process.

It is an abridged review (a reliance pathway).

Regional regulatory initiatives can help optimize the efficient use of an agency’s resources. The following countries participate in this initiative/pathway: Brunei Darussalam Cambodia Indonesia Lao People's Democratic Republic Malaysia Myanmar Philippines Singapore Thailand Vietnam

Review of applications will start only after all participating NRAs have received the application(s) and related documentation and have considered it accepted for assessment.