Regulation 3

The fees specified in the First Schedule are payable to the Authority for the manufacture, import, supply and registration of CTGT products under the CTGTP Regulations.

The fees specified in the Second Schedule are payable to the Authority for the manufacture, import and supply of clinical research material under the CRM Regulations.

The fees specified in the Third Schedule are payable to the Authority for the submission of a notification under regulation 4 of the CP‑ACD Regulations.

The fees specified in the Fourth Schedule are payable to the Authority for an application for a certificate under regulation 3 of the GMPC‑CP Regulations.

The fees specified in the Fifth Schedule are payable to the Authority in relation to retail pharmacies and the supply of certain health products under the LRP Regulations.

The fees specified in the Sixth Schedule are payable to the Authority for the manufacture, import, supply and registration of medical devices under the MD Regulations.

The fees specified in the Seventh Schedule are payable to the Authority for the manufacture, import, supply, registration and advertisement of oral dental gums under the ODG Regulations.

The fees specified in the Eighth Schedule are payable to the Authority for the manufacture, import, supply and registration of therapeutic products under the TP Regulations.

The fees specified in the Ninth Schedule are payable to the Authority for the manufacture, import and supply of active ingredients under the AI Regulations.