A supplier does not supply a prohibited carcinogen (Schedule 10 table 10.1) unless the recipient provides evidence that it is for genuine research or analysis and the regulator has authorised it under r 384 or granted an exemption, and does not supply a restricted carcinogen (table 10.2) for a listed use without evidence of such authorisation or exemption; it records the recipient and the name and quantity supplied and keeps the record for 5 years after the last supply.
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.