Cap. 458 Art. 37Manufacturer’s licence.

Without prejudice to any exemption that may be granted under this Act, no person shall import from countries which are outside the European Union or European Economic Area, manufacture, assemble or in any way modify any medicinal product except in accordance with a manufacturer’s licence issued in accordance with the provisions of this Act or any regulations or rules made thereunder: Provided that such a licence shall not be required for the preparation, division, changes in packaging or presentation where these processes are carried out for the purpose of dispensing or administering as provided under this Act.