Schedule 5

FIFTH SCHEDULERegulations 40KA(a) and 40KC(1)Part 1PRESCRIBED INDUSTRIES AND PRESCRIBED WATER EFFICIENCY REQUIREMENTS FOR SECTION 40 OF ACTFirst column Second columnPrescribed industry Prescribed water efficiency requirement

1. Biomedical and Pharmaceutical (1)Manufacture of cell, tissue or gene therapy products Recycle all specified waste streams(2)Manufacture of contact lenses Recycle all specified waste streams(3)Manufacture of cosmetic products Recycle all specified waste streams(4)Manufacture of medical devices Recycle all specified waste streams(5)Manufacture of medicated oil or balm Recycle all specified waste streams(6)Manufacture of oral dental gum Recycle all specified waste streams(7)Manufacture of quasi-medicinal products Recycle all specified waste streams(8)Manufacture of therapeutic products Recycle all specified waste streams

2. Electronics (1)Manufacture of electronic products or components, such as batteries, capacitators, display screens, hard disks, printed circuit boards and sensors Recycle all specified waste streams(2)Manufacture of semiconductor products, such as diodes, radio frequency filters and photomasks Recycle all specified waste streams(3)Manufacture of semiconductor wafers from ingots Recycle all specified waste streams(4)Testing and assembly of semiconductor chips Recycle all specified waste streams

3. Wafer fabrication (1)Front-end fabrication of semiconductor circuits from blank wafers, that is, from the start of fabrication to before individual semiconductor circuits are separated from the blank wafers Achieve a minimum recycling rate of 50%(2)Front-end fabrication of semiconductor wafers from blank wafers, that is, from the start of fabrication to before individual semiconductor wafers are separated from the blank wafers Achieve a minimum recycling rate of 50%Part 2DEFINITIONSIn this Schedule —“cell, tissue or gene therapy product” has the meaning given by the First Schedule to the Health Products Act 2007;“cosmetic product” has the meaning given by the First Schedule to the Health Products Act 2007;“medical device” has the meaning given by the First Schedule to the Health Products Act 2007;“medicated oil or balm” has the meaning given by the First Schedule to the Health Products Act 2007;“oral dental gum” has the meaning given by the First Schedule to the Health Products Act 2007;“quasi-medicinal product” has the meaning given by the First Schedule to the Health Products Act 2007;“recycling rate” means the rate of recycling determined in accordance with the method set out in the PUB S&R Standard for Water Efficiency;“specified waste stream” means a reject stream of water generated from any of the following processes: