Χώρα: Αυστραλία
Γλώσσα: Αγγλικά
Πηγή: APVMA (Australian Pesticides and Veterinary Medicines Authority)
Vaccine - greasy pig
APVMA PERMIT
Vaccine - greasy pig
PIG HEALTH & RESEARC
vaccine
Vaccination against greasy pig disease caused by Staphylococcus hyicus with an unregistered product.
Registered and available
2016-03-10
PER12551 Permit Version 4 Page 1 of 4 PERMIT TO ALLOW MINOR USE AND SUPPLY OF AN AGVET CHEMICAL PRODUCT PERMIT NUMBER -PER12551 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. 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 12 JANUARY 2011 TO 28 FEBRUARY 2018. PERMIT HOLDER: PIG SERVICES CENTRE Cnr Taylor Street and Midland Highway EPSOM VIC 3551 SUPPLIER: PIG SERVICES CENTRE Cnr Taylor Street and Midland Highway EPSOM VIC 3551 PERSONS WHO CAN USE THE PRODUCT UNDER THIS PERMIT: Registered veterinary surgeons and persons acting under their direction. PRODUCT TO BE USED (THE PRODUCT): Autogenous _Staphylococcus hyicus_ vaccine Containing 1 x 10 9 cfu/mL of inactivated_ Staphylococcus hyicus, _as the only active constituent. PER12551 Permit Version 4 Page 2 of 4 DIRECTIONS FOR USE: ANIMAL PURPOSE DOSAGE AND ADMINISTRATION Pigs Vaccination against greasy pig disease caused by _Staphylococcus hyicus_ 2 Doses; 2mL IM , 3 weeks apart JURISDICTION: All States SUPPLY 1. The Holder 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 Resources biological import permit must be provided on request. d. In-proces Διαβάστε το πλήρες έγγραφο