1. A copy of the actual Special Import Licence granted by the Department in respect of Gamaret 2. A copy of the application for a Special Import Licence XXX for Gamaret. 3. Details of the shortage of supply of frontline intra-mammary formulations prevailing at the time (particularly when not only was Terexine available, but there was also available a product, Synulox, manufactured by XXXX). 4. Details of the problem in production and market supply as advised to the Department from a key number of multi-nationals specifying the product and the manufacturer/multi-national concerned. 5. All documentation/working papers passing between XXX and the Department. 6. All documentation passing between the Department and XXX/XXX 7. All particulars of the application process of XXX or such party as holds the Special Import Licenses XXX for Gamaret. 8. Particulars of why XXX was not invited to participate in the application process. 9. On what grounds opinion was expressed that Terexine was not an appropriate available animal remedy, authorised within the State. 10. All updates received in respect of Tetra delta and its availability. 11. Details concerning communications between the Minister and the XXX about the proposed importation of Gamaret.