Snapshot

The Marketing Authorization of Non In-Vitro Diagnostic Medical Devices for Human Use pathway has been developed by the of Zambia.

This pathway can be used where Non In-Vitro Diagnostic Medical Devices.

This pathway accelerates the regulatory review process.

It is an abridged review (a reliance pathway).

Target time assessment is An application shall be evaluated on a first come first serve basis unless expedited evaluation has been authorized by the Authority. .