Cap. 458 чл. 105Recognition of equivalent standards.

For the purposes of this Act, the Minister may, on the advice of the Licensing Authority, by regulations prescribe that a provision or provisions in relation to the marketing authorisation of a medicinal product shall be deemed to be satisfied, if the standards of manufacture, medicinal product quality, safety or efficacy, or the provisions in relation to the granting of a marketing authorisation of a country designated in such regulations, are satisfied.