fediaf guide to good practice
DESCRIPTION
FEDIAF Guide to Good practice. for the Manufacture of Safe Pet Food TRAINING PACKAGE Module VIII Production. 8. PRODUCTION TOPICS. 8.1 General requirements 8.2Presence of genetically modified organism 8.3 Feed materials of animal origin 8.4 Weighing 8.5 Mixing - PowerPoint PPT PresentationTRANSCRIPT
![Page 1: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/1.jpg)
FEDIAF Guide to Good practice
for the Manufacture of Safe Pet FoodTRAINING PACKAGE
Module VIIIProduction
![Page 2: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/2.jpg)
8. PRODUCTION TOPICS
8.1 General requirements8.2 Presence of genetically modified organism8.3 Feed materials of animal origin8.4 Weighing8.5 Mixing8.6 Quality control and product analysis8.7 Temperature/time control8.8 Foreign body detection8.9 Product release8.10 Control of non-conforming goods8.11 Quantity control8.12 Equipment and process validation8.13 Calibration8.14 Specific handling requirements8.15 Product packaging
![Page 3: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/3.jpg)
8.1 General requirements8.2 Presence of genetically modified organism (GMO)
8.1 Clear responsibilities and production procedures Employee responsible for production quality Production stages documented Measures to ensure hygiene and safety
8.2 Procedures in place to control GMO (adventitious or unavoidable: 0.9% threshold)
In case of contamination cleaning obligatory GMO-free declaration of supplier necessary
![Page 4: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/4.jpg)
8.3 Feed materials of animal origin8.4 Weighing
8.3 Feed material of animal origin must comply with legislation
Category 3 material packed preventing leakage Must be labelled: “Pet food only”
8.4 Accurate weighing equipment Appropriate devices and regular calibration Regular maintenance programme
![Page 5: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/5.jpg)
8.5 Mixing
8.5 Homogeneous mixture is essential Homogeneity must be verified. Clean, appropriate and maintained
mixers Mixers operate for a pre-set time Mixing efficiency regularly checked Prevent unacceptable carry over of
undesirable substances
![Page 6: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/6.jpg)
8.6 Quality control/analysis
8.6 Quality Control Plan (QCP) in place Identify CCPs and OPRPs Modifications must be managed Analytical testing for shelf life, chemical factors etc. External laboratories to be accredited
Critical Control Point
![Page 7: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/7.jpg)
8.7 Temperature/time control
8.7 Temperature controlled• recorded when critical to product safety Use alarm systems for monitoring Ensure hygienic conditions after heat treatment
SterilisationPseudo D Value Plot at 121.1 C
for Cl. botulinum
0
1
2
3
4
5
6
7
0 0.25 0.5 0.75 1 1.25 1.5 1.75 2
Time in Minutes
Cou
nt o
f Org
anis
m
Fc
![Page 8: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/8.jpg)
8.8 Foreign body detection8.9 Product release
8.8 Identify, eliminate, minimise foreign body contamination Determine CCPs & OPRPs Where necessary, install detectors Corrective actions after detection
8.9 Pet food released by authorised personnel Release procedures for each batch
Foreign body detector
![Page 9: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/9.jpg)
8.10 Control non-conforming goods8.11 Quantity control8.12 Equipment/process validation
8.10 Out-of-specification products must be identified, labelled, quarantined Corrective actions8.11 Quantity checks to verify conformity with EU law Equipment regularly calibrated legally accepted8.12 Processing methods and validate product data in case of
changes or failures
Control panel
![Page 10: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/10.jpg)
8.13 Calibration8.14 Handling requirements
8.13 Equipments: calibrated, records documented
8.14 Specific procedures to ensure safety • Potentially risky packaging (glass) • Reprocessing and reworking
Records documented
![Page 11: FEDIAF Guide to Good practice](https://reader036.vdocuments.mx/reader036/viewer/2022062301/5681633f550346895dd3cfdd/html5/thumbnails/11.jpg)
8.15 Product packaging
8.15 Use proper packaging materials Packaging: conform with specifications Protect packaging surplus before store it again Packaging material stored apart from raw materials
Finished product being transported