S.L. 417.3 Art. 2Interpretation. Cap. 417.

In these regulations, unless the context otherwise requires -"Act" means the Patents and Designs Act;

"certificate" means a supplementary protection certificate issued by the Comptroller for the purposes of these regulations; "Comptroller" means the Comptroller of Industrial Property;

"medicinal product" means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals; "patent" rneans a patent as defined in the Act, in relation to a product; "product" means the active ingredient or combination of active ingredients of a medicinal product and includes the process to obtain such product or an application of such product.