Section 15
Licences
(1)
The Authority may, subject to the provisions of this Act, issue any of the following licences and the application therefor shall be made in such form and manner, and shall contain, or be accompanied by, such documents, items, samples, particulars and other information, as the Authority may require. The following licences shall only be issued after an inspection, except a clinical trial import licence —
(a)
an import licence, authorising the licensee to import, store and sell by wholesale or supply the registered products from the premises specified in licence;
(b)
a manufacturer’s licence, authorising the licensee to manufacture the registered products in the premises specified in the licence and to sell by wholesale or supply the products;
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(c)
a wholesaler’s licence, authorising the licensee to sell by wholesale or supply the registered products from the business premises specified in the licence;
(d)
a clinical trial import licence, authorising the licensee to import one product for the purpose of clinical trials, notwithstanding that the product is not a registered product.
(2)
If medicines products are not included together in one licence, any number of registered products may be included in any licence other than a clinical trial import licence.
(3)
Subject to subsection (2), the Authority may, on application by the licensee, add to the registered products included in any licence, other than a clinical trial import licence, and make such addition or amendment to the conditions of the licence as are rendered necessary by the addition of such added products.
(4)
Subject to section 20, a licence issued under this Act, other than a clinical trial import licence, shall be valid for one year.
(5)
Subject to section 20, a clinical trial import licence shall be valid for such period, not exceeding 3 years from the date of issue of the licence, as may be specified in the licence.
(6)
Every licence is not transferable to any other person.