Uht Processing and Aseptic Filling of Dairy Foods
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Module 3 Online Quiz
IAHCSMM CCSVP Vendor Education Program Module Three Assembly and Packaging Introduction: • Once items have been decontaminated and made safe to handle, they are assembled and packaged. While this may sound simple, it is a multi-step process that requires several technical skills. • This module is designed to provide you with an overview of the inspection, assembly and packaging processes. Objectives: • Upon completion of this module, you will be able to: – List the steps in instrument inspection and assembly – Explain the impact that positioning and placement of instruments has on sterilization processes – Identify common packaging methods – List factors that can impact assembly and packaging outcomes Instructions • Read Chapters 10, 11 and 12, in the IAHCSMM Central Service Technical Manual, Eighth Edition, 2016. • Review this module. • Complete the online quiz for Module Three . Central Service Technicians… …are responsible for the quality of instruments. Instrument Manufacturing • Forging • Note: Instruments are • Grinding and Milling inspected throughout • Assembly their manufacturing process. • Heat Tempering • Polishing • Passivation • Final Inspection • Etching Passivation A chemical process applied during instrument manufacture that provides a corrosion-resistant finish by forming a thin transparent oxide film. Reminder: • Be sure to watch the Instrument Manufacturing Process Video from “How It’s Made” that accompanies this unit. Post-operative Care of Surgical Instruments • Keep instruments moist. Do not allow blood to dry on -
Guidelines for the Design and Construction Of
Guidelines for the Design and Construction of Stormwater Management Systems Developed by the New York City Department of Environmental Protection in consultation with the New York City Department of Buildings July 2012 Michael R. Bloomberg, Mayor Carter H. Strickland, Jr., Commissioner Cover: An extensive green roof system installed atop the NYC Department of Parks and Recreation’s (DPR) Five Borough Building on Randall’s Island. This modular system is one of six variations installed on the roof and covers 800 square feet, con- sisting of two-foot by two-foot trays with six inches of mineral soil and over 1,500 sedum plugs. DPR has installed 25 green roof systems covering over 29,000 square feet on the Five Borough Building rooftop to feature different types and depths of growing medium and plant selection. Dear Friends; The NYC Green Infrastructure Plan, released in September 2010, proposed an innovative ap- proach for cost-effective and sustainable stormwater management. A major part of this plan is our commitment to manage the equivalent of an inch of rainfall on ten percent of the impervious areas in combined sewer watersheds by 2030. To that end, DEP is prepared to spend $1.5 bil- lion to construct green infrastructure projects across the city. Yet public investment alone will not achieve our water quality goals, or our desired recreation and development opportunities. Some of the most cost-effective opportunities are represented by new construction and devel- opment, when stormwater source controls can be easily included in designs and built at a frac- tion of the cost of retrofitting existing buildings. -
Food Packaging (FS 522 / FS 495) Aseptic Processing and Packaging
Food Packaging (FS 522 / FS 495) Aseptic Processing and Packaging Components of an aseptic processing system Aseptic processing is a thermal process in which the product and container are sterilized separately and brought together in a sterile environment. It involves pumping, deaeration, and sterilization of a food product, followed by holding it for a specified period of time (in a holding tube -- required to have a 1/4" rise per foot length of tube), cooling it, and finally packaging it in a sterile container. The use of high temperature for a short period of time (in comparison with conventional canning) in aseptic processing yields a high quality product. Care should be taken to ensure that all process calculations are performed after the deaeration stage and not based on the initial raw product. Deaeration is accomplished in a vessel maintained at a certain degree of vacuum by means of a vacuum pump. The product is fed into the vessel at 55 - 70 /C through a nozzle at the center of the vessel. Vacuum is controlled to obtain a product flash of about 5 /C. An internal spiral condenser condenses vapors and other condensable gases. The deaerated product is discharged through the bottom and pumped to the heating section. Another important part of an aseptic processing system is the back pressure valve which provides sufficient pressure to prevent boiling of the product at processing temperatures which can be as high as 125-130 /C. An aseptic surge tank provides the means for product to be continuously processed even if the packaging system is not operational due to any malfunction. -
WHO Good Manufacturing Practices for Sterile Pharmaceutical Products
© World Health Organization WHO Technical Report Series, No. 961, 2011 Annex 6 WHO good manufacturing practices for sterile pharmaceutical products Introduction Following implementation of these WHO good manufacturing practices (GMP) guidelines (1) within the context of the WHO Prequalifi cation of Medicines Programme, clarifying, editorial modifi cations have been proposed. These changes were adopted for maintenance purposes. In order to ease reading the full guideline has been reproduced again as an Annex to the current report of the WHO Expert Committee on Specifi cations for Pharmaceutical Preparations. WHO good manufacturing practices for sterile pharmaceutical products 1. General considerations 2. Quality control 3. Sanitation 4. Manufacture of sterile preparations 5. Sterilization 6. Ter minal sterilization 7. Aseptic processing and sterilization by fi ltration 8. Isolator technology 9. Blow/fi ll/seal technology 10. Personnel 11. Premises 12. Equipment 13. Finishing of sterile products References Further reading 261 1. General considerations 1.1 The production of sterile preparations should be carried out in clean areas, entry to which should be through airlocks for personnel and/or for equipment and materials. Clean areas should be maintained to an appropriate standard of cleanliness and supplied with air that has passed through fi lters of the required effi ciency. 1.2 The various operations of component preparation (such as those involving containers and closures), product preparation, fi lling and sterilization should be carried out in separate areas within the clean area. These areas are classifi ed into four grades (see section 4). 1.3 Manufacturing operations are divided here into two categories: —fi rst, those where the product is terminally sterilized; and — second, those which are conducted aseptically at some or all stages. -
130 Innovative Steam Injection for Milk Processing
Innovative Steam Injection for Milk Processing Ekta Mistry, J. P. Prajapati and Suneeta V. Pinto Department of Dairy Technology, SMC College of Dairy Science, AAU, Anand-388110. Email: [email protected] Ultra High Temperature (UHT) treatment uses high Studies reported on UHT processing have temperature for a short time to kill micro-organisms been concerned mostly with indirect heating in a food or beverage product. It is widely used in systems. This method of processing has been in the dairy industry where products can easily lose commercial use since 1949 (Burton, 1969). Use their nutritional value, flavour and appearance as of indirect heating system results in 75% to 90 % microorganisms multiply. These organisms thrive denaturation of whey proteins. In 1972, the United at certain temperatures but if they are not present States Public Health Service approved the use of in a product, it can be stored for many months UHT steam injection for pasteurization of milk without the need for refrigeration. This state is (Stroup et al., 1972). Lembke and Wegener (1968) known as ‘commercial sterility’. UHT processes indicated that UHT direct steam injection is less are designed to achieve commercial sterility. They destructive to the aqueous and lipid portions than use heat to treat the product, killing viable micro- indirect UHT heating techniques. This is mainly organisms. This aseptic processing also requires due to rapid heating (steam injection) and cooling equipment and packaging to be sterile, achieved (vacuum) of the product. However, direct steam Technical Articles Technical with chemical or other sterilisation treatments (de injection also results in 65-85% denaturation of Jong, 2008). -
Pasteurization and Its Discontents: Raw Milk, Risk, and the Reshaping of the Dairy Industry Andrea M
University of Vermont ScholarWorks @ UVM Graduate College Dissertations and Theses Dissertations and Theses 2015 Pasteurization and its discontents: Raw milk, risk, and the reshaping of the dairy industry Andrea M. Suozzo University of Vermont Follow this and additional works at: https://scholarworks.uvm.edu/graddis Part of the Agriculture Commons, Communication Commons, and the Food Science Commons Recommended Citation Suozzo, Andrea M., "Pasteurization and its discontents: Raw milk, risk, and the reshaping of the dairy industry" (2015). Graduate College Dissertations and Theses. 320. https://scholarworks.uvm.edu/graddis/320 This Thesis is brought to you for free and open access by the Dissertations and Theses at ScholarWorks @ UVM. It has been accepted for inclusion in Graduate College Dissertations and Theses by an authorized administrator of ScholarWorks @ UVM. For more information, please contact [email protected]. PASTEURIZATION AND ITS DISCONTENTS: RAW MILK, RISK AND THE RESHAPING OF THE DAIRY INDUSTRY A Thesis Presented By Andrea Suozzo To The Faculty of the Graduate College Of The University of Vermont In Partial Fulfillment of the Requirements for the Degree of Master of Science Specializing in Food Systems January 2015 Defense Date: August 28, 2014 Thesis Examination Committee: Amy Trubek, Ph.D., Advisor Sarah N. Heiss, Ph.D., Advisor David Conner, Ph.D., Chair Cynthia J. Forehand, Ph.D., Dean of the Graduate College ABSTRACT Milk is something many Americans consume every day, whether over cereal, in coffee or in a cup; as yogurt, cream, cheese or butter. The vast majority of that milk is pasteurized, or heated to the point where much of the bacteria in the milk dies. -
IAC 3/11/09 Pharmacy[657] Ch 13, P.1 CHAPTER 13 STERILE
IAC 3/11/09 Pharmacy[657] Ch 13, p.1 CHAPTER 13 STERILE COMPOUNDING PRACTICES 657—13.1(124,126,155A) Purpose and scope. These rules establish standards and procedures for the preparation, labeling, and distribution of sterile preparations by licensed pharmacies pursuant to a practitioner’s order or prescription; for sterile product quality and characteristics; for personnel training, environmental quality, and equipment standards; and for pharmaceutical care. Sterile compounding differs from nonsterile compounding primarily by requiring the maintenance of sterility when preparations are compounded exclusively with sterile ingredients and components and by requiring the achievement of sterility when preparations are compounded with nonsterile ingredients and components. The standards and procedures outlined in this chapter apply to pharmacy practice when a preparation: 1. Is prepared according to the manufacturer’s labeled instructions and requires other manipulations that expose the original contents to potential contamination; 2. Contains nonsterile ingredients or employs nonsterile components or devices that must be sterilized before administration; or 3. Is a biologic, diagnostic, drug, or nutrient that possesses characteristics of either “1” or “2” above and includes, but is not limited to, the following preparations that are required to be sterile when they are administered to patients: baths and soaks for live organs and tissues, injections (e.g., colloidal dispersions, emulsions, solutions, and suspensions), aqueous bronchial and -
Pasteurization Effects on Yield and Physicochemical Parameters Of
a ISSN 0101-2061 (Print) ISSN 1678-457X (Online) Food Science and Technology DOI: https://doi.org/10.1590/fst.13119 Pasteurization effects on yield and physicochemical parameters of cheese in cow and goat milk Dahmane TADJINE1, Sofiane BOUDALIA2,3* , Aissam BOUSBIA2,3, Rassim KHELIFA4, Lamia MEBIROUK BOUDECHICHE1, Aicha TADJINE5, Mabrouk CHEMMAM2,3 Abstract Cheese production is one of the most common forms of valorization of dairy production, adding value and preserving milk. Various types of cheese produced from raw and pasteurized milk are known worldwide. In the present work, we are interested in studying the effect of the type of milk (raw and pasteurized) of two species (cow and goat) on the yield and physicochemical characteristics of the fresh cheese. In the northeastern Algeria, on 5 cow farms and 3 goat farms; 5 raw and 5 pasteurized milk cheese manufacturing trials were conducted. The analysis of the results of the 80 samples of milk and cheese of both cow and goat species showed that the latter contained significantly more fat and protein than cow’s milk and that pasteurized milk contained more protein than raw milk. As a result, actual cheese yield of goat cheese was higher than that of cows in pasteurized and raw milk. For higher yield, our result supported the use of pasteurized milk as a raw material in the manufacture of farmhouse cheese. Keywords: cheese yield; manufacturing; pasteurized; raw milk; livestock. Practical Application: For cheese-making under small scale using milk from cow or goat: pasteurization can increase actual cheese yield. 1 Introduction In Algeria, as in all regions of the world, consumption of have been attributed to several indigenous microbiota, such dairy products like cheeses is an old tradition linked to livestock as Lactococcus spp., Lactobacillus spp., Leuconostoc spp., and farming, since dairy products are made using ancient artisanal Enterococcus spp. -
Microbiological Safety of Cheese Made from Heat-Treated Milk, Part I
441 Journal of Food Protection, Vol. 53, No. 5, Pages 441-452 (May 1990) Copyright© International Association of Milk, Food and Environmental Sanitarians Microbiological Safety of Cheese Made from Heat-Treated Milk, Part I. Executive Summary, Introduction and History ERIC A. JOHNSON1, JOHN H. NELSON1*, and MARK JOHNSON2 Food Research Institute and the Walter V. Price Cheese Research Institute, University of Wisconsin, Madison, Wisconsin 53706 Downloaded from http://meridian.allenpress.com/jfp/article-pdf/53/5/441/1660707/0362-028x-53_5_441.pdf by guest on 30 September 2021 (Received for publication August 2, 1989) ABSTRACT four decades, the United States cheese industry produced over 100 billion pounds of natural cheese (not including Research on pasteurization of milk for cheesemaking was cottage and related varieties). The most frequent causative begun in the late 1800's. Early equipment was crude and control factor in U.S. and Canadian cheese-related outbreaks was devices non-existent. Consequently, early pasteurization proc post-pasteurization contamination. Faulty pasteurization esses were not well verified. Commercial application was slow, equipment or procedures were implicated in one outbreak except in New Zealand, where almost the entire cheese industry converted to pasteurization in the 1920's. In the United States, each in the U.S. and Canada. Use of raw milk was a factor debate on the merits of pasteurization continued for years. Demand in one outbreak in each country. Inadequate time-tempera for cheese during World War II and foodborne disease outbreaks ture combinations used for milk heat treatment were not caused by cheese stimulated promulgation of government stan implicated. -
Chapter 288. Dairy Industry
CHAPTER 288. DAIRY INDUSTRY DAIRY PRODUCTS Act 169 of 1929 288.1-288.15 Repealed. 1956, Act 216, Eff. July 1, 1957;—1965, Act 233, Eff. June 30, 1966;—1965, Act 385, Eff. June 30, 1966. FLUID MILK ACT OF 1965 Act 233 of 1965 288.21-288.29a Repealed. 1996, Act 91, Imd. Eff. Feb. 27, 1996;—2001, Act 266, Eff. Feb. 8, 2002. BREED NAMES OF DAIRY CATTLE Act 139 of 1939 288.41-288.45 Repealed. 1964, Act 256, Eff. Aug. 28, 1964. MILK FAT TEST LAW Act 212 of 1935 288.51-288.60 Repealed. 1984, Act 52, Imd. Eff. Apr. 12, 1984;—2001, Act 267, Eff. Feb. 8, 2002. MILK AND MILK PRODUCTS Act 216 of 1956 288.71-288.83 Repealed. 1965, Act 233, Eff. June 30, 1966;—1965, Act 385, Eff. June 30, 1966. MANUFACTURING MILK ACT Act 222 of 1913 288.101-288.117 Repealed. 1973, Act 201, Imd. Eff. Jan. 11, 1974;—1993, Act 134, Eff. Apr. 1, 1994 ;—1996, Act 361, Imd. Eff. July 2, 1996;—2001, Act 267, Eff. Feb. 8, 2002. PROCESSING DAIRY PRODUCTS BY STEAM INFUSION Act 91 of 1962 288.121-288.126 Repealed. 1967, Act 22, Eff. Nov. 2, 1967. PASTEURIZATION OF MILK AND MILK PRODUCTS Act 291 of 1947 288.131-288.137 Repealed. 1967, Act 45, Eff. Nov. 2, 1967. PASTEURIZATION OF MILK AND MILK PRODUCTS Act 45 of 1967 288.141-288.149 Repealed. 2001, Act 267, Eff. Feb. 8, 2002. PASTEURIZATION OF MILK AND OTHER DAIRY PRODUCTS Act 293 of 1945 288.151-288.153 Repealed. -
Town of Fairfield Recycling Faqs
Item How to dispose Acids Hazardous waste To find the item you are looking for hold the Aerosol can (food grade only, empty) Put this item in your recycling bin. <Command> or <Ctrl> key + the letter "F" down together, type the item in the box in the Aerosol can (food grade only, (full or partially full) Put this item in your trash. upper right of your screen Aerosol can (NON food grade only, empty) Put this item in your trash. and press <Return> or <Enter>. NOTE: the first key noted is for Mac, the second key noted is Aerosol can (NON food grade only, (full or for PC. partially full) Take this to Hazardous waste Air Conditioner Put in Electronics trailer at the transfer station ( small fee) Aluminum baking tray Put in Recycling Bin - Clean it prior Aluminum foil Put in Recycling Bin - Clean it prior Aluminum Pie Plate Put in Recycling Bin - Clean it prior Ammunition Contact the Police department Animal waste and Bedding Put this item in your trash. Anti Freeze Bring to transfer station Consider donating to local school or creative reuse center. If they contain toxic Art Supplies materials, they should be brought to a Household Hazardous Waste collection event or facility. If not, place this item in the trash for disposal. Connecticut Department of Public Health recommends that a licensed asbestos Asbestos contractor abate the material. Put this item in your recycling bin., Loose caps go in the trash, remove and put any Aseptic Carton, such as a milk carton straws in the trash Ash - Coal Cool ash completely, Put in Bag in trash Ash - Charcoal Gripp Cool ash completely, Put in Bag in trash Ash - Manufactured logs and pellets Cool ash completely, Put in Bag in trash Consider starting a compost bin or food waste collection service ; otherwise put in Baked Goods Trash Balloon Put this item in your trash. -
Aseptic Processing White Paper
WHITE PAPER ASEPTIC PROCESSING WHILE MAINTAINING PRODUCT INTEGRITY Published by Marlen A MARLEN WHITE PAPER: Aseptic Processing While Maintaining Product Integrity INTRODUCTION Aseptic processing and packaging is one of the most dynamic areas of food processing. Although invented in the middle of the twentieth century, recently a panel of food technologists and scientists from the Institute of Food Technologists (IFT) with the intention of identifying leading food processing and packaging achievements advised that “Aseptic processing is the most significant food science development in the last 50 years.” The most basic definition of aseptic processing is the independent sterilization of the product followed by filling and sealing (packaging) in sterile containers in a sterile environment. Also known as high-temperature-short-time (HTST) processing, more and more processors are realizing the benefits of aseptic processing and packaging. Therefore, the number of processors utilizing this technology has significantly increased. With the recent advent of the U.S. Food and Drug Administration approval of aseptic processing of food products containing particulate matter, we expect this method of food processing to explode with activity. Marlen pumps facilitate this and fulfill one of the most critical areas of the process. THE PROBLEM In addition to extending the life of shelf stable products, processors must protect heat-sensitive products such as produce, soups, sauces and baby food from microbial degradation. Until recently, continuous thermal aseptic processing solutions using ultra-high temperatures were not approved by the U.S. Food and Drug Administration, forcing processors to use low acid canned food (LACF) methods that compromised the nutritional and organoleptic properties of the food products.