Page 187 - Small Animal Clinical Nutrition 5th Edition
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Commercial Pet Foods        189



                  trol points can be established around unit operations and qual-  nonconforming product is identified and removed. This fre-
        VetBooks.ir  ity systems set up to monitor and ensure conformance. The  quency depends on batch sizes, length of storage and normal
                                                                      ingredient variation history. Sampling every 30 minutes for
                  manufacturing process of pet foods primarily involves proper
                                                                      moisture, protein, fat, calcium, phosphorus, sodium, potassium
                  compounding of raw ingredients and then working this mixture
                  for moist or dry extruded products.Therefore, quality programs  and magnesium to determine variation in the process is a good
                  must include: 1) calibration procedures for conveying the indi-  starting point. Samples can be analyzed either separately or as
                  vidual ingredients, 2) proper time and temperature measuring  a composite sample collected over time if the manufacturing
                  and 3) calibration procedures for the cooking process. For moist  process is well controlled.
                  products, the sterilization program must be documented and  For dry pet foods, sampling should include: 1) each lot of raw
                  recorded. Detailed records should be kept for each lot of prod-  ingredients received, 2) the mix of raw ingredients once com-
                  uct manufactured, clearly detailing the processing conditions.  pounded (weighed and mixed), 3) the product leaving the
                  Routine, clearly documented calibration and correlation pro-  extruder, 4) the product leaving the dryer, 5) after any topical
                  grams must be established for each process variable (i.e., weigh-  enrobing and 6) finished product in the package. For moist pet
                  ing or scaling, temperatures, flow rates, etc.). Analytical and  foods, samples should be taken from: 1) raw materials, 2) prod-
                  physical testing of finished product is another essential element  uct in the cooker/mixer and 3) sterilized product.
                  of a good quality program.
                                                                      Statistical Process Control
                  Vendors                                             To ensure the most consistent quality of the finished product,
                  Pet foods contain numerous raw materials from many suppli-  modern factories use statistical process control in the manufac-
                  ers. A vendor quality control program is critical to ensuring  turing process. Statistical process control determines normal
                  receipt of high-quality raw ingredients.            variation through chemical analysis of the product at various
                    A good quality vendor control program begins with: 1) test-  points in the process compared with nutrient specifications of
                  ing methods for nutrient levels, 2) microbiologic evaluation and  the finished product. It also establishes control limits based on
                  3) toxicity testing. Defining these test methods ensures that  this variation.
                  multiple vendors of raw ingredients deliver against the same  Variables analyzed can be moisture, protein, fat or any other
                  purchasing specification. A routine calibration and correlation  nutrient of concern for a particular product where consistency
                  program should be established to minimize method and oper-  is required. Usually, two to three standard deviations from the
                  ator variations. A vendor quality program should establish the  mean represent the control limits. Adjustments to the manu-
                  frequency of analytical testing; however, each lot of an ingredi-  facturing process are made only when finished product attrib-
                  ent must be tested initially for moisture, protein and fat, at a  utes are outside these control limits.
                  minimum, to see if it adheres to ingredient specifications and
                  for accurate compounding. Ingredients should also be routine-  Analytical Tests
                  ly analyzed for other nutrients of concern (e.g., calcium, phos-  Finished products are analyzed to ensure conformity to formu-
                  phorus, magnesium and sodium).                      lated nutrient content and freedom from toxins and microbio-
                    Beyond the testing required in a purchasing specification,  logic concerns. At a minimum, a good quality program should
                  further quality assurance can be attained through programs the  include routine testing to determine percentages of moisture,
                  food industry calls vendor self-certification. The objective of  protein, fat, ash, calcium, phosphorus, sodium, magnesium,
                  these programs is to shift the focus from final ingredient ship-  potassium and crude fiber. Additionally, incoming raw ingredi-
                  ment testing to building of quality control procedures upstream  ents and finished products should be tested for Salmonella and
                  in the vendors’ process. For example, purchasing specifications  Clostridium species, aflatoxin and vomitoxin.
                  for cereal grains would include a target value for percent mois-  Each manufacturing facility should have an in-house labora-
                  ture of the grain. Most certification programs require vendors  tory that can run the above analyses as the product is produced.
                  to keep detailed records on the lots of material they purchase.  The results help operators adjust the process controls to ensure
                  The intent is to encourage vendors to define, understand and  the finished product meets specifications. Faster analytical
                  control their raw materials and processes so that they manufac-  methods (e.g., near infrared) that can analyze several nutrients
                  ture and supply ingredients that will fall within the pet food  simultaneously with speed and accuracy help operators control
                  manufacturer’s specifications.                      the process. In addition to chemical analysis, the physical size,
                                                                      density and color should be part of the finished product speci-
                  Product Quality                                     fications. In the case of canned pet foods, can seal, product tex-
                  The quality of the finished pet food product is quantified by  ture and vacuum should be recorded in addition to chemical
                  how well the product meets the formulated nutrient content  analysis results.
                  as well as other critical parameters, such as: 1) consistent
                  appearance, 2) physical integrity, 3) package integrity, 4) ade-  Shelf Life
                  quacy of sterilization and 5) freedom from toxins and micro-  Shelf life is the amount of time a product maintains nutrition-
                  biologic concerns.                                  al, microbial, physical and organoleptic (sensory) integrity. The
                    Sampling frequency should be established to ensure that any  main cause of diminished shelf life in dry products is oxidation.
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