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Regulation 135 Amendment of regulation 168 (use of non-prescription medicines in the course of a business)

Original text. Later amendments are not shown.

In regulation 168, in paragraph (8)—

(a)

in sub-paragraph (a), for “EEA State” substitute “approved country for import”; and

(b)

for sub-paragraph (b) substitute—

“(b)

imported from an approved country for import—

(i)

it is manufactured or assembled in that country by a person who is the holder of an authorisation in that country in relation to its manufacture or assembly, and

(ii)

it is imported by the holder of a wholesale dealer’s licence under Part 3 that includes the import of a medicinal product from such a country.”.