As enacted

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National Medicines Regulatory Authority Act 2015 · As enacted · Part IV · General

113. Licensing of premises for manufacturing &c., of medicine &c

Official English translation. Where it differs from the Sinhala or Tamil text, the Act itself says which text prevails.

(1)

No person shall manufacture, prepare, store or sell any medicine, medical device or borderline product in any premises unless such premises has been licensed in that regard by the Authority.

(2)

(a)

No person shall store or sell any medicine, medical device or borderline product, in any premises unless such premises has been licensed by the Authority.

(b)

The provisions of paragraph (a) shall not apply to—

(i)

any patient who keeps any medicine, medical device or borderline product registered under this Act, for his personal use;

(ii)

any medicine, medical device or borderline product prescribed by regulations as safe for general use.

(3)

The Authority shall maintain a register of registered manufacturers and importers and the criteria for registering shall be as prescribed.

Read on from s 114

Part V