Country: Ástralía
Tungumál: enska
Heimild: APVMA (Australian Pesticides and Veterinary Medicines Authority)
Pasteurella multocida
APVMA PERMIT
Pasteurella multocida
ANIMAL CONSULT. ENT.
vaccine
To control disease caused by Pasteurella multocida in pigs and poultry (Permit restricted to use by approved person/s).Permit restricted to use by approved person/s.
Registered and available
2016-01-20
PER12580 Permit Version 3 Page 1 of 7 PERMIT TO ALLOW SUPPLY AND MINOR USE OF AN AGVET CHEMICAL PRODUCT PERMIT NUMBER - PER12580 This permit is issued to the Permit Holder in response to an application granted by the APVMA under section 112 of the Agvet Codes of the jurisdictions set out below. This permit allows a Supplier (as indicated) to possess The Product for the purposes of supply and to supply The Product to a person who can use The Product under permit. If this permit were not issued, supply of The Product as specified below would constitute an offence under section 78 of the Agvet Code. This permit also allows a person, as stipulated below, to use The Product in the manner specified in this permit in the designated jurisdictions. This permit also allows the Permit Holder, the Supplier (if not one and the same) and any person stipulated below to claim that The Product can be used in the manner specified in this permit. THIS PERMIT IS IN FORCE FROM 20 JANUARY 2011 TO 31 MARCH 2020. PERMIT HOLDER: ANIMAL CONSULTING ENTERPRISES P/L 12 Gildea lane BENDIGO EAST VIC 3550 SUPPLIER: ANIMAL CONSULTING ENTERPRISES P/L 12 Gildea lane BENDIGO EAST VIC 3550 PERSONS WHO CAN USE THE PRODUCT UNDER THIS PERMIT: Registered veterinarians and people under their direction. PRODUCT TO BE USED: CUSTOM INACTIVATED PASTEURELLA MULTOCIDA VACCINE FOR PIGS AND POULTRY Containing _Pasteurella multocida _as the only active constituent. DIRECTIONS FOR USE: ANIMAL PURPOSE DOSE Pigs and Poultry To control disease caused by As per the attached label _Pasteurella multocida_ PER12580 Permit Version 3 Page 2 of 7 CONDITIONS SUPPLY 1. Animal Consulting Enterprises may supply the Product to registered veterinarians if: a. The preparation of the Product is restricted to cultures of microorganisms which have been inactivated and are non-toxic. b. The Product must be prepared in a GMP category 1 (immunobiologicals) licensed facility. c. Where imported biological materials are used, evidence of current Department of Agriculture and Water Resource Lestu allt skjalið