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Standard Registration Requirements
___ Completed application package per T-3-20 (Application for Feed Registration and
Ingredient Approval)
Proposed Label
___ Brand name (optional)
___ Product name reflecting purpose of the product and the intended
species
___ Product claim statement
___ Guaranteed analysis (active ingredients)
___ Complete list of ingredients by generic name as listed in Schedule IV or V
of Feed Regulations including registration numbers for Part II ingredients or
mixed feeds, as required
___ Directions for use to permit safe and effective use of the feed
___ Caution and/or warning statements (if applicable)
___ Name and address of registrant
___ Net amount (metric measure)
___ Registration number (to be added)
Product Composition
___ Formulation / percentage composition listing amount of each ingredient by
generic name as listed in Schedule IV or V of Feed Regulations including
registration numbers for Part II ingredients or mixed feeds
___ Formulation / Ingredients - verify level of ingredients does not exceed
maximums per Schedules IV and V.
Scientific Studies
___ Scientific studies are required to support the intended purpose of these
products and must be provided for our review
___ Studies carried out by qualified personnel
___ Suitable methods used in studies
___ Studies designed to facilitate statistical analysis. The research design
must include at least 3 replicates of each treatment involved, including the
control.
___ Data analysed by appropriate statistical methods
___ Studies conducted under conditions similar to those that may be expected
to occur in Canada
___ Scientific investigations show that the product, when used as directed,
significantly (P<0.05) improves pellet durability in a
specific feed for a specific class of livestock.
___ When the pellet binder is intended for use in a variety of feeds and/or
for various classes of livestock, scientific investigations must show
significant differences (P<0.05) between the control and
treated groups, for each of the specific feeds and/or livestock groups where
the product is intended for use
___ Where the directions for use indicate a range of inclusion rates, the
testing protocol must evaluate the lowest inclusion rate.
___ Where results of these studies have not been published in a refereed
journal, copies of the raw data and printouts of statistical analysis are
required for our review.
Sample
___ Provided (if necessary to validate lab methodology)
Promotional Claims (including Internet and Advertising)
___ Consistent with stated purpose of product
NOTE: Further information may be required after a review of the
submission.
For more information, please contact:
Feed Section
Animal Health & Production Division
Canadian Food Inspection Agency
59 Camelot Drive
Nepean, Ontario, Canada K1A 0Y9
Telephone: (613) 225-2342
Facsimile: (613) 228-6614
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