DingLiSheng Technology is a Shenzhen-based company established in 2005 that manufactures inflatable packaging materials like air bags, bubbles, and cushions. It has a 200,000 square meter factory near Shenzhen airport. DingLiSheng produces over 3.5 million packaging items per month using imported equipment, and has certifications like ISO9001, ISO14000, SGS, and REACH. It offers environmentally friendly packaging that is lightweight, saves space, and reduces costs for over 1,000 customers worldwide.
Process for producing leather-like material and material obtainable therebyToscana Open Research
This patent application describes a process for producing a leather-like material from leather waste. The process involves mechanically reducing leather scraps into fibers, mixing them with a thermoplastic polymer, heating the mixture to melt the polymer, extruding the material, and cooling to produce the final product. The resulting material has physical properties similar to real leather and can be used in applications like footwear, clothing, and furniture.
This document discusses key considerations for the aseptic manufacturing of sterile pharmaceutical products. It covers classification of clean areas, environmental monitoring, preparation and filtration of solutions, personnel requirements, equipment sterilization, and validation of aseptic processes. The main objectives are to prevent microbial contamination and maintain sterility throughout manufacturing.
This document summarizes the process of creating plastic roads. Plastic waste is collected, cleaned, shredded, and mixed with heated bitumen and aggregate. This plastic-coated aggregate mix is then used to construct rural roads. Benefits include reducing the need for bitumen by 10% and costs by around Rs. 5000/km while creating jobs and providing an eco-friendly solution for plastic waste. Potential issues are the need to properly clean toxic materials from waste plastic and prevent the leaching of fine polymer particles after construction. The document concludes that plastic roads could help decrease environmental pollution in India's climate.
The document discusses the construction, working, validation process, and qualification protocols for a fluidized bed dryer (FBD) used in pharmaceutical applications. It describes the key components of an FBD and the fluidization drying process. Validation of the FBD involves design, installation, operational, and performance qualifications to ensure proper functioning.
This document provides information about cleanrooms, their classification, design, and testing. It defines cleanrooms and classifications based on maximum allowable particle concentrations. ISO classification ranges from 1 to 9, with lower numbers indicating cleaner rooms. Design considerations include personnel and material flows, air flow patterns to minimize contamination, construction materials for cleanability, and HVAC systems for air filtration and pressure differentials between zones. Parameters like particle levels, air changes, temperature and humidity are monitored regularly to maintain cleanroom quality.
This document provides an overview of sales and use tax rules for manufacturers in Wisconsin. It discusses what qualifies as manufacturing and what purchases are exempt, such as equipment, ingredients, fuel and containers used directly in manufacturing. It also covers documentation needed to prove exemptions and defines terms like "direct use" and "qualified research". Manufacturers must pay use tax on items not taxed by vendors and properly classify sales as taxable or exempt.
Shobak, Refrigerated Vertical Door Display CabinetHARIS K.E.
This document provides information about the Shobak Vertical Door Display Cabinet made by Haris Industrial Kitchen and Catering Equipment. The cabinet has insulated polyurethane foam walls for even temperature control. It uses a fan-assisted cooling system and electronic controls to efficiently regulate temperature and defrosting. The slim frame and full-glass doors maximize visibility while allowing for a large display area.
FACTORS IN THE DESIGN OF PARENTERAL PRODUCTION FACILITIESNEHA SINGH
THIS PRESENTATION DESCRIBE ABOUT DIFFERENT FACTORS RELATED TO PARENTERAL PREPARATION OR PRODUCTION MAINLY AND HAVE DIFFERENT SPECIAL TERMS RELATED TO PARENTERAL DEPARTMENT ,BENEFECIAL FOR THE PHARMACY STUDENTS BOTH B.PHARM OR M.PHARM OR BIOTECHNOLOGY MAINLY
Process for producing leather-like material and material obtainable therebyToscana Open Research
This patent application describes a process for producing a leather-like material from leather waste. The process involves mechanically reducing leather scraps into fibers, mixing them with a thermoplastic polymer, heating the mixture to melt the polymer, extruding the material, and cooling to produce the final product. The resulting material has physical properties similar to real leather and can be used in applications like footwear, clothing, and furniture.
This document discusses key considerations for the aseptic manufacturing of sterile pharmaceutical products. It covers classification of clean areas, environmental monitoring, preparation and filtration of solutions, personnel requirements, equipment sterilization, and validation of aseptic processes. The main objectives are to prevent microbial contamination and maintain sterility throughout manufacturing.
This document summarizes the process of creating plastic roads. Plastic waste is collected, cleaned, shredded, and mixed with heated bitumen and aggregate. This plastic-coated aggregate mix is then used to construct rural roads. Benefits include reducing the need for bitumen by 10% and costs by around Rs. 5000/km while creating jobs and providing an eco-friendly solution for plastic waste. Potential issues are the need to properly clean toxic materials from waste plastic and prevent the leaching of fine polymer particles after construction. The document concludes that plastic roads could help decrease environmental pollution in India's climate.
The document discusses the construction, working, validation process, and qualification protocols for a fluidized bed dryer (FBD) used in pharmaceutical applications. It describes the key components of an FBD and the fluidization drying process. Validation of the FBD involves design, installation, operational, and performance qualifications to ensure proper functioning.
This document provides information about cleanrooms, their classification, design, and testing. It defines cleanrooms and classifications based on maximum allowable particle concentrations. ISO classification ranges from 1 to 9, with lower numbers indicating cleaner rooms. Design considerations include personnel and material flows, air flow patterns to minimize contamination, construction materials for cleanability, and HVAC systems for air filtration and pressure differentials between zones. Parameters like particle levels, air changes, temperature and humidity are monitored regularly to maintain cleanroom quality.
This document provides an overview of sales and use tax rules for manufacturers in Wisconsin. It discusses what qualifies as manufacturing and what purchases are exempt, such as equipment, ingredients, fuel and containers used directly in manufacturing. It also covers documentation needed to prove exemptions and defines terms like "direct use" and "qualified research". Manufacturers must pay use tax on items not taxed by vendors and properly classify sales as taxable or exempt.
Shobak, Refrigerated Vertical Door Display CabinetHARIS K.E.
This document provides information about the Shobak Vertical Door Display Cabinet made by Haris Industrial Kitchen and Catering Equipment. The cabinet has insulated polyurethane foam walls for even temperature control. It uses a fan-assisted cooling system and electronic controls to efficiently regulate temperature and defrosting. The slim frame and full-glass doors maximize visibility while allowing for a large display area.
FACTORS IN THE DESIGN OF PARENTERAL PRODUCTION FACILITIESNEHA SINGH
THIS PRESENTATION DESCRIBE ABOUT DIFFERENT FACTORS RELATED TO PARENTERAL PREPARATION OR PRODUCTION MAINLY AND HAVE DIFFERENT SPECIAL TERMS RELATED TO PARENTERAL DEPARTMENT ,BENEFECIAL FOR THE PHARMACY STUDENTS BOTH B.PHARM OR M.PHARM OR BIOTECHNOLOGY MAINLY
This document discusses the design and operation of an aseptic area for producing sterile pharmaceutical products. It describes the different sections of the aseptic area including the clean-up, compounding, aseptic, quarantine, and packaging/labeling areas. It provides details on airflow, filtration, surfaces, clothing, cleaning procedures, and sources of potential contamination. The goal is to maintain sterile conditions and limit contamination that could compromise the sterile products being produced.
The document discusses aseptic filling techniques used to minimize contamination during manufacturing of sterile drug products. It outlines three main areas of control: environmental control through clean rooms and HVAC systems, equipment control using sterilization and sanitization, and individual control with personnel hygiene and gowning. Key aspects covered include clean room classification, HEPA filters, air locks, laminar flow hoods, sterilization methods, and environmental monitoring to ensure an aseptic environment is maintained.
The document discusses various packaging and food processing equipment, including their working principles, advantages, and disadvantages. It covers vacuum packaging machines, form fill and seal machines, cup fillers, and automatic water bottling machines. The key points are:
- Vacuum packaging machines remove air from packages to extend food freshness and reduce spoilage. Form fill and seal machines vertically or horizontally form tubes from plastic film, fill them with products, and seal the packages.
- Cup fillers use measuring cups to volumetrically fill free-flowing products like nuts or grains. Automatic water bottling machines integrate bottle rinsing, filling, and capping into one machine to automate the water bottling process.
A clean room is an environment with controlled levels of particulate contamination defined by international standards. Clean rooms minimize introduction and retention of particles through HEPA filtration of air, controlled airflow, temperature, humidity and pressure. Contamination is classified as particulate, chemical, biological or radiation. People are the largest contamination source. Clean rooms require strict personal hygiene, protective clothing, and environmental controls to maintain the clean environment for pharmaceutical manufacturing as defined by regulations like ISO, GMP and FDA standards.
Packaging textiles include all textile packing material for industrial, agricultural and other goods
It is used to contain, carry, store, and protect goods
Packing material demand and economic growth, industrial production and trade
Growing need for reusable packages & containers gives a new opportunities for textile products
Technical textiles, used in packaging & subsequent transportation are called “PACKTECH.”
This document summarizes the manufacturing process for an aseptic still juice drink. The main objectives are low production cost, high quality products, high automation and flexibility, and high reliability. The process involves blending juice concentrate, sugar, and other ingredients; HTST pasteurization to kill pathogens while preserving quality; and aseptic filling and packaging into PET bottles with a 6-month shelf life. Key steps are blending for consistency and quality, HTST pasteurization using a plate heat exchanger for safety and low energy use, and aseptic packaging through sterilization and filling of bottles and caps under sterile conditions.
This document provides guidance on cleanroom classifications and air quality standards for the manufacture of sterile products. It outlines four grades (A, B, C, D) for clean areas based on required airborne particulate and microbial limits. Grade A is for high-risk operations like filling and requires laminar airflow. Grades B, C, D are for less critical processes. Air quality standards are provided for "at rest" and "in operation" states. Monitoring of clean areas during production is recommended to control particulate and microbial levels.
This document provides an overview of sterile product manufacturing. It discusses personnel requirements including training, gowning, and medical checks. Building and premises must have specifically designed clean rooms with proper HVAC, water, and equipment. Processes like component preparation, product filling, and sterilization require different air classifications. Sterilization methods include moist heat, dry heat, irradiation, ethylene oxide, and filtration. Quality control, sanitation, documentation, and validation are vital to ensuring sterile products are safe for patients.
Packtech refers to packaging textiles used for protection, distribution, labeling, customer convenience, selling, and promoting brands during transportation and storage. This document discusses various types of packtech products including polyolefin woven sacks, flexible intermediate bulk containers (FIBC), leno bags, wrapping fabric, jute sacks, tea bags, and soft luggage products. It also outlines the roles, reasons for use, categories, advantages, and important global market for packtech textiles.
Understanding types of ink migration in food, pharmaceutical, and health and beauty packaging. Overview of the 10 Good Manufacturing Practices (GMPs) to reduce risk.
The document discusses design requirements for aseptic manufacturing facilities. Key points include:
- Facility design must facilitate appropriate space, operations, material and waste flows to prevent contamination.
- Critical areas require stringent controls for airborne particles, air changes, airflow velocity, and surface cleanliness.
- Utilities like WFI, steam, and HVAC systems must be designed to stringent quality standards to prevent contamination.
- Documentation and validation are required to prove the facility is built as designed and certified for use.
This document provides information on sterile dosage forms and parenteral preparations. It defines sterile dosage forms as pharmaceutical products that must be free from living microorganisms due to their route of administration. Parenteral preparations include solutions, suspensions, and other dosage forms administered via injection. The document outlines the key areas and equipment needed for manufacturing parenteral preparations in a sterile environment, including clean rooms, laminar airflow workstations, and filling areas. It also provides a brief overview of ophthalmic preparations and their requirements.
This document provides an overview of various packaging machines used in the packaging process. It describes filling machines that fill bottles or pouches, including agitator filling machines, flow filling machines, and tablet fillers. It also discusses sealing machines that securely close packages, such as food packaging machines, vacuum packaging machines, and blister packaging machines. The document further describes labeling machines that apply labels to packages and end-of-line equipment like case sealers, sleeve wrappers, case erectors, case packers, and palletizers.
This document provides an overview of a presentation on pharmaceutical packaging and development with a focus on pediatric formulations. It discusses choosing appropriate primary packaging, regulatory considerations, extractables and leachables testing, and packaging development processes. Specific topics covered include blister packs, bottles, closures, barrier properties of materials, desiccants, oxygen and water vapor transmission rates, and first intent guidelines.
Este documento describe las diferencias entre medios de comunicación síncronos y asincrónos. Explica que las herramientas asincrónicas como el correo electrónico y los foros permiten la colaboración de personas que no trabajan al mismo tiempo, mientras que las herramientas síncronas como el chat y las videoconferencias facilitan la colaboración en tiempo real. También proporciona ejemplos como Skype de herramientas síncronas y lista algunas modalidades educativas como la enseñanza presencial, semipresenc
Problema 1: Dibujar una superficie reglada de tres directrices, siendo la velocidad de avance en la directriz central constante.
Problema 2: Dibujar un hiperboloide elíptico.
The document provides a summary of Jamie Barker's qualifications, skills, work history, and education for a shipping/receiving/inventory control position. It outlines over 20 years of experience in warehouse environments, including packaging, shipping, receiving, inventory control, forklift operation, data entry, and meeting various productivity and safety metrics. It also lists current and past employer experience from 2015 to 2002 in similar warehouse roles, as well as certificates in forklift operation, small engine repair, WHMIS, and first aid.
Laura S. Downing has over 20 years of experience working in libraries, including as a cataloging librarian, reference and instruction librarian, head of reference, and scholarly communications librarian at the Dean B. Ellis Library of Arkansas State University. She holds an M.L.I.S. from University of Wisconsin-Milwaukee and a B.A. in English from Minnesota State University. Downing has published several encyclopedia entries and presented widely at conferences on topics related to library resources and scholarly research. She has served on numerous professional committees and holds memberships in the American Library Association and Sigma Alpha Iota.
Charles Cilny Strong is an experienced producer, director, writer, and business consultant with 20 years of experience in entertainment law and large event production. He has produced global online peace summits and environmental festivals, and currently provides strategic planning and digital content services to nonprofit organizations focused on veterans entrepreneurship, men's empowerment, and public libraries. Strong has expertise in legal and contract administration, creative and digital media production, and social media marketing.
El documento describe un experimento para demostrar la dilatación térmica de los materiales. En el experimento, dos frascos con agua coloreada son sellados con sorbetes y silicona y sumergidos en agua hirviendo. En el frasco lleno hasta el tope, el agua no cambia, mientras que en el frasco parcialmente lleno el agua sube por el sorbete, mostrando cómo la dilatación del vidrio hace que aumente el volumen del líquido.
This document discusses the design and operation of an aseptic area for producing sterile pharmaceutical products. It describes the different sections of the aseptic area including the clean-up, compounding, aseptic, quarantine, and packaging/labeling areas. It provides details on airflow, filtration, surfaces, clothing, cleaning procedures, and sources of potential contamination. The goal is to maintain sterile conditions and limit contamination that could compromise the sterile products being produced.
The document discusses aseptic filling techniques used to minimize contamination during manufacturing of sterile drug products. It outlines three main areas of control: environmental control through clean rooms and HVAC systems, equipment control using sterilization and sanitization, and individual control with personnel hygiene and gowning. Key aspects covered include clean room classification, HEPA filters, air locks, laminar flow hoods, sterilization methods, and environmental monitoring to ensure an aseptic environment is maintained.
The document discusses various packaging and food processing equipment, including their working principles, advantages, and disadvantages. It covers vacuum packaging machines, form fill and seal machines, cup fillers, and automatic water bottling machines. The key points are:
- Vacuum packaging machines remove air from packages to extend food freshness and reduce spoilage. Form fill and seal machines vertically or horizontally form tubes from plastic film, fill them with products, and seal the packages.
- Cup fillers use measuring cups to volumetrically fill free-flowing products like nuts or grains. Automatic water bottling machines integrate bottle rinsing, filling, and capping into one machine to automate the water bottling process.
A clean room is an environment with controlled levels of particulate contamination defined by international standards. Clean rooms minimize introduction and retention of particles through HEPA filtration of air, controlled airflow, temperature, humidity and pressure. Contamination is classified as particulate, chemical, biological or radiation. People are the largest contamination source. Clean rooms require strict personal hygiene, protective clothing, and environmental controls to maintain the clean environment for pharmaceutical manufacturing as defined by regulations like ISO, GMP and FDA standards.
Packaging textiles include all textile packing material for industrial, agricultural and other goods
It is used to contain, carry, store, and protect goods
Packing material demand and economic growth, industrial production and trade
Growing need for reusable packages & containers gives a new opportunities for textile products
Technical textiles, used in packaging & subsequent transportation are called “PACKTECH.”
This document summarizes the manufacturing process for an aseptic still juice drink. The main objectives are low production cost, high quality products, high automation and flexibility, and high reliability. The process involves blending juice concentrate, sugar, and other ingredients; HTST pasteurization to kill pathogens while preserving quality; and aseptic filling and packaging into PET bottles with a 6-month shelf life. Key steps are blending for consistency and quality, HTST pasteurization using a plate heat exchanger for safety and low energy use, and aseptic packaging through sterilization and filling of bottles and caps under sterile conditions.
This document provides guidance on cleanroom classifications and air quality standards for the manufacture of sterile products. It outlines four grades (A, B, C, D) for clean areas based on required airborne particulate and microbial limits. Grade A is for high-risk operations like filling and requires laminar airflow. Grades B, C, D are for less critical processes. Air quality standards are provided for "at rest" and "in operation" states. Monitoring of clean areas during production is recommended to control particulate and microbial levels.
This document provides an overview of sterile product manufacturing. It discusses personnel requirements including training, gowning, and medical checks. Building and premises must have specifically designed clean rooms with proper HVAC, water, and equipment. Processes like component preparation, product filling, and sterilization require different air classifications. Sterilization methods include moist heat, dry heat, irradiation, ethylene oxide, and filtration. Quality control, sanitation, documentation, and validation are vital to ensuring sterile products are safe for patients.
Packtech refers to packaging textiles used for protection, distribution, labeling, customer convenience, selling, and promoting brands during transportation and storage. This document discusses various types of packtech products including polyolefin woven sacks, flexible intermediate bulk containers (FIBC), leno bags, wrapping fabric, jute sacks, tea bags, and soft luggage products. It also outlines the roles, reasons for use, categories, advantages, and important global market for packtech textiles.
Understanding types of ink migration in food, pharmaceutical, and health and beauty packaging. Overview of the 10 Good Manufacturing Practices (GMPs) to reduce risk.
The document discusses design requirements for aseptic manufacturing facilities. Key points include:
- Facility design must facilitate appropriate space, operations, material and waste flows to prevent contamination.
- Critical areas require stringent controls for airborne particles, air changes, airflow velocity, and surface cleanliness.
- Utilities like WFI, steam, and HVAC systems must be designed to stringent quality standards to prevent contamination.
- Documentation and validation are required to prove the facility is built as designed and certified for use.
This document provides information on sterile dosage forms and parenteral preparations. It defines sterile dosage forms as pharmaceutical products that must be free from living microorganisms due to their route of administration. Parenteral preparations include solutions, suspensions, and other dosage forms administered via injection. The document outlines the key areas and equipment needed for manufacturing parenteral preparations in a sterile environment, including clean rooms, laminar airflow workstations, and filling areas. It also provides a brief overview of ophthalmic preparations and their requirements.
This document provides an overview of various packaging machines used in the packaging process. It describes filling machines that fill bottles or pouches, including agitator filling machines, flow filling machines, and tablet fillers. It also discusses sealing machines that securely close packages, such as food packaging machines, vacuum packaging machines, and blister packaging machines. The document further describes labeling machines that apply labels to packages and end-of-line equipment like case sealers, sleeve wrappers, case erectors, case packers, and palletizers.
This document provides an overview of a presentation on pharmaceutical packaging and development with a focus on pediatric formulations. It discusses choosing appropriate primary packaging, regulatory considerations, extractables and leachables testing, and packaging development processes. Specific topics covered include blister packs, bottles, closures, barrier properties of materials, desiccants, oxygen and water vapor transmission rates, and first intent guidelines.
Este documento describe las diferencias entre medios de comunicación síncronos y asincrónos. Explica que las herramientas asincrónicas como el correo electrónico y los foros permiten la colaboración de personas que no trabajan al mismo tiempo, mientras que las herramientas síncronas como el chat y las videoconferencias facilitan la colaboración en tiempo real. También proporciona ejemplos como Skype de herramientas síncronas y lista algunas modalidades educativas como la enseñanza presencial, semipresenc
Problema 1: Dibujar una superficie reglada de tres directrices, siendo la velocidad de avance en la directriz central constante.
Problema 2: Dibujar un hiperboloide elíptico.
The document provides a summary of Jamie Barker's qualifications, skills, work history, and education for a shipping/receiving/inventory control position. It outlines over 20 years of experience in warehouse environments, including packaging, shipping, receiving, inventory control, forklift operation, data entry, and meeting various productivity and safety metrics. It also lists current and past employer experience from 2015 to 2002 in similar warehouse roles, as well as certificates in forklift operation, small engine repair, WHMIS, and first aid.
Laura S. Downing has over 20 years of experience working in libraries, including as a cataloging librarian, reference and instruction librarian, head of reference, and scholarly communications librarian at the Dean B. Ellis Library of Arkansas State University. She holds an M.L.I.S. from University of Wisconsin-Milwaukee and a B.A. in English from Minnesota State University. Downing has published several encyclopedia entries and presented widely at conferences on topics related to library resources and scholarly research. She has served on numerous professional committees and holds memberships in the American Library Association and Sigma Alpha Iota.
Charles Cilny Strong is an experienced producer, director, writer, and business consultant with 20 years of experience in entertainment law and large event production. He has produced global online peace summits and environmental festivals, and currently provides strategic planning and digital content services to nonprofit organizations focused on veterans entrepreneurship, men's empowerment, and public libraries. Strong has expertise in legal and contract administration, creative and digital media production, and social media marketing.
El documento describe un experimento para demostrar la dilatación térmica de los materiales. En el experimento, dos frascos con agua coloreada son sellados con sorbetes y silicona y sumergidos en agua hirviendo. En el frasco lleno hasta el tope, el agua no cambia, mientras que en el frasco parcialmente lleno el agua sube por el sorbete, mostrando cómo la dilatación del vidrio hace que aumente el volumen del líquido.
A Formal Model for Enabling RFID in Pharmaceutical Supply ChainsMatthieu Schapranow
The document summarizes a presentation given at the 44th Hawai’i International Conference on System Sciences about enabling RFID technology in pharmaceutical supply chains. It describes a formal model for representing supply chain entities and roles, presents a quantitative analysis of network traffic for a sample US supply chain, and evaluates security considerations for different roles. The model accounts for relationships between business entities and handling units from individual items to transport vehicles. Network traffic is estimated at 234.92TB annually for a supply chain with 15 billion goods and 7 links. Security is addressed through authentication, on-tag mechanisms, and a proposed "service provider for anti-counterfeiting" role.
1) El documento habla sobre la importancia de desarrollar competencias laborales para ser competitivo en el mercado laboral actual. 2) Define las competencias básicas, conductuales y funcionales que se necesitan, las cuales se obtienen a través de la educación y experiencia. 3) Explica que las escuelas y universidades deben enseñar estas competencias que son fundamentales para el éxito laboral.
The Business of F&B Innovation - Chef Steven Carlcourageasia
The document discusses innovation in the context of menu development for restaurants. It provides definitions of innovation and discusses how innovation involves applying better solutions to meet new or existing needs in a practical way. The document then lists several food trends to consider for menus, such as comfort foods, global foods, raw foods, sharable foods, low-alcohol drinks, and healthy snacks. It emphasizes starting with existing menu items and ideating incremental improvements, then testing ideas. The goal of innovation is developing a better solution for a defined need.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have strict quality control systems in place and certifications like ISO 9001, cGMP, and BRC. PET Power uses an injection stretch blow moulding process to produce bottles and jars in a cleanroom facility, and can provide gamma irradiation for sterilization. They offer various bottle and jar styles, sizes, and colors for pharmaceutical and medical applications.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow moulding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various laboratory services to support product development and regulatory requirements for their pharmaceutical customers.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow molding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various bottle styles, closures, and lab services to support customers' packaging needs.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have strict quality control systems in place and certifications like ISO 9001, cGMP, and BRC. PET Power uses an injection stretch blow moulding process to produce bottles and jars from PET resin in a cleanroom facility classified as ISO Class 7. Finished products undergo sterilization with gamma radiation to achieve a sterility assurance level of 10^-6.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow moulding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various laboratory services to support product development and regulatory requirements for their customers in the healthcare industry.
Vacuum forming is a manufacturing process that uses heat and suction to form plastic sheets over molds. A plastic sheet is first clamped and heated, then placed over a mold and pulled into shape using vacuum pressure. The plastic cools and is then removed, trimmed, and finished. Vacuum forming offers lower costs than other plastic processes for smaller production runs. It is used to produce food packaging, medical devices, automotive and industrial parts, and more, using various heat-formable plastic materials. While affordable for simple parts, vacuum forming has limitations for complex geometries with thin walls.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are manufactured in a cleanroom facility and can be gamma irradiated for sterility. The document provides details on PET Power's production processes, quality controls, certifications and laboratory services to support customers in the healthcare industry.
PET Power is a leading specialist in PET packaging for the healthcare industry. They have a quality management system certified to ISO 9001:2008 and cGMP standards. Products are manufactured in a cleanroom facility classified as ISO Class 7 and Class 8. Quality control testing is performed on all products, including 100% leak testing. Traceability is ensured through a labeling system that tracks production details. Optional gamma irradiation is used to sterilize products upon customer request.
PET Power is a leading specialist in PET packaging for the healthcare industry. They have a quality management system certified to ISO 9001:2008 and cGMP standards. Their cleanroom facilities include ISO Class 7 and 8 cleanrooms for pharmaceutical packaging. Quality control testing is performed on products, including 100% leak testing. Traceability is enabled through unique identification on each package.
Medium efficiency pocket bag f7 fine air filter with micro glass fiber for an...BarbaaSmirnow1
This document describes medium efficiency pocket/bag F7 fine air filters produced by Guangzhou Airy Filter Media Co., Ltd. It provides specifications for various filter models with different sizes, pocket counts, efficiency levels, and pressure drop rates. The filters use non-woven materials and micro glass fiber to avoid harm. They are mainly used in automotive manufacturing, nuclear power, electronics, and other industries requiring high dust holding capacity. Guangzhou Airy Filter Media is a filter manufacturer and trader with over 12 years of experience producing various air filter types.
ㅁFor faster, healthier hand drying
Bio JetDryer is a breakthrough in hand drying. It uses a high power motor to create warm air that will dry your hands in around ten seconds. It’s elegant, ultra-modern, and a joy to use. It’s also better for the environment thanks to its low power consumption. And it’s much more hygienic than alternatives. In most of our models a quadruple antibacterial filter prevents the spread of bacteria and viruses, keeping the unit clean and hygienic at all times.
Elegant, hygienic and cost-effective
Biodrier is the hygienic, fast, efficient and stylish way to dry hands in any washroom. Bio JetDryer is based on a simple yet powerful idea – Using the heat from its own motor to provide the warm air required to dry the user’s hands. This means it uses much less power than conventional hot air hand dryers.
Keeps walls and floors dry
To use the Bio JetDryer, simply pop your hands in, and the three infrared sensors commence the warm air. The Bio JetDryer supplies gentle, but powerful gusts of high-speed air to both sides of your hands (Business and Executive models only). After around ten seconds remove your hands and they’re completely dry.
A high-speed vacuum motor saves energy as it consumes from only 1150 watts of power. The shorter drying time combined with lower power consumption saves money and reduces your carbon footprint!
Bio JetDryer is also unbelievably quiet and in some of our models it produces a natural aroma that is both refreshing and relaxing. The design is also ergonomically stylish and elegant.
Save time, save money, save energy!
The largest exporters of vacuum bagging and composite tooling materials for prepreg/autoclave, resin infusion, and wet lay-up processes is Airtech Advanced Materials Group. With nearly 50 years of extrusion experience, Airtech is your local source for vacuum bagging materials, composite tooling producers, and 3D Print knowledge. For more details: https://airtech.com/
Design and Development of Humidity Controller for Prevention of Microbiologic...IRJET Journal
The document describes the design and development of a humidity controller to prevent microbiological spoilage in vegetables. Key points:
- A hot air drying system was developed using an air heater boiler, fans, temperature sensors, and an isolated cabin to dry vegetables. This reduces drying time from 3-4 days conventionally to 7-8 hours.
- The system aims to maintain optimal humidity levels between 45-55% for drying different vegetables like tomatoes and ginger.
- Trials showed the developed system successfully dried vegetables and maintained desired temperatures and humidity levels in different weather conditions.
This document discusses Good Manufacturing Practices (GMP) for sterile pharmaceutical products. It provides an agenda that covers requirements for facilities, equipment, processes, and documentation for sterile manufacturing. Key points include maintaining proper air handling systems with appropriate air classification grades for different areas. Environmental monitoring, garment requirements, sanitation procedures, equipment specifications, and detailed manufacturing and batch documentation standards are also outlined to ensure sterile products are consistently manufactured and controlled to quality standards.
This document discusses clean air solutions from Camfil, including their products for particle and molecular air filtration. It summarizes several of Camfil's filter product lines for applications such as indoor air quality, cleanrooms, and odor removal. These products include the City-Flo high performance bag filter, CityPleat pre-filter, City M air purifier, Gigapleat compact molecular filters, and exchangeable panel molecular filters. The document emphasizes Camfil's focus on health, sustainability, comfort, and process protection through high efficiency air filtration.
With years of experience and a commitment to excellence, we have become a trusted supplier of filter products for various industries worldwide. Whether you're looking for a single filter product or need to outfit your entire facility, our factory has everything you need to get the job done. So why wait? Contact us today to learn more about our products and services and see how we can help you keep your workplace clean, safe, and productive.
Yancheng Vision Manufacture Technology Co., Ltd is a leading manufacturer of industrial filter products in China, our factory is committed to providing customers with a full range of high-quality filter products at unbeatable prices. From dust filter bags and filter bag cages to industrial filter cartridges and HVAC filters, we have everything you need to keep your workplace clean and safe.
2. Shenzhen DingLiSheng Technology Co.,Ltd was established
in 2005, which located in Shajing town, Bao’an District,
Shenzhen, adjacent to the ShenZhen airport and FuYong
dock, so the traffic is very convenient, also the factory covers
an area of 200 million square meters.
Dinglisheng is engaged in the inflating bags, air
bags, air column bags, filling bags, anti-static
bags, kraft paper bubble bags etc. And it also
has passed the ISO9001:2008 international
quality system, ISO14000 environment system
certification, SGS/ROHS, REACH138
certifications.
3. Several sets of imported production equipment, 3.5 million/month
production capacity:
Processing bags
workshop
Imported production
equipment
9. Why choose us?
♦ The world's first production scale
♦ High performance/price ratio, and green environmental protection
♦ More than one thousand users worldwide
♦ Committed to new packaging development
♦ Saving space
♦ High safety
♦ The cost reduction
♦ Low carbon environmental protection
10. Independent air
column, local
damage does
not affect the
product use
Reverse leakage
technology
Personal
protective air
bag arranged
type
Reverse leakage valve technology
Personal protective air bag arranged
type
99% of natural air and 1% of co-
extrusion plastic film
shatterproof, antiwear, outstanding
protection function
11. DingLiSheng Products completely flat before not
inflatable transportation convenient integration 。
Release the air, after using product healing state into the
recycling system.
12. put the product inside
Filling the air
packing
completed
The air bag from DingLiSheng Made up by multilayer functional
resin film, using the check valve check technology layers of resin
film by heat sealing and fold constitute a space that can deposit
gas medium, to use the air to reach the purpose of buffering.
The air bag from DingLiSheng Made up by multilayer functional
resin film, using the check valve check technology layers of resin
film by heat sealing and fold constitute a space that can deposit
gas medium, to use the air to reach the purpose of buffering.
The air-bags which form DingLiSheng
are the best packing materials to
instead of EPS and EPE.
To decrease the
carton size.
A
B
13. Buffer performance: the whole package, using the air shrinkage as a buffer.
lose weight + decrement + Alternative to
other materials at the same time satisfy the
requirements of the product's transport
protection.
Buffer performance has a wide application fields
From the daily consumption, logistics in the
field of consumer electronics and so on,
products from dozens of grams to dozens of
kilograms, inflatable packaging can have very
good protection effect.
500pcs The finished
product packing
The smallest packing
carton size.
14. For long distance transport.
Quick shipment.
Standardized production, better
quality
In view of the RoHS have better
control
DingLiSheng To export-oriented
and global enterprises of
supply chain management,
standards and the quality of the
chemicals to provide effective,
safety guarantee
One stop purchasing Global transportation
15. The least amount
of storage space.
Convenient
logistics
management
Weight reduction,decrement
From multiple links such as production, transport, reduce
carbon emissions.
Cleaner Delivery
16. anti-static Can be printedWaterproof,
moistureproof
Improve the image of the product:
Products are clean, simple and
professional.
17. Dell packing group in 3 C: Cube,Content and Curb
To interpret the new packaging design concept, designed to improve efficiency, save money,
for the user at the same time help them become a leader in environmental protection.
We are very proud of becoming one member of the Dell global green packaging
strategy plan !!
After DingLiSheng's packaging solution :
-Saving 10-15% of the material
- Greatly reduces the engineering build time
-To improve the customers to use feeling
-Reduce the material usage and cost/reduced the waste
into the landfill facilities
-Very good goods delivery conditions
-Reduce the logistics cost
-Reduces the packing labor costs
-From each production link is cancelled 140 need to use
pallet flow program
-Environmental and recycling advantage
Directly reduce the cost more than 3.5 million
euros per year, embodied in the following several
major success:
1. A year to save the cost for packaging materials
980000 euros to 980000 euros
2. Workers cost savings for euro 1.4 m letters of
1.4 million euros
3.Logistics cost saving the euro 1.12 m letters of
1.12 million euros
4. From each production link is cancelled 140 need
to use pallet flow program
5. Environmental and recycling of edge
18. Through the standardization of design and
production, solve the various products
Bring up material management of waste.
The original outer carton packaging is
increased by 15% than products
The weight of packaging materials
Comprehensive personal air cushion
packaging provides the best shockproof,
prevent fall protection
By combining different process to provide
a variety of functions, thus effectively
reducing the use of different packaging
material
By heat seal airtight, waterproof,
moistureproof
19. Inflatable cushion combined
with logistics Courier bag
Packaging steps :
1.In the need to transport
products and invoice
2.Heat sealing cushion the inner
bag
3.Charging operation
4.Sealing glue to go
5.Finished product packing to
shipment
21. Products display
Red wine air bag wine air bag Tablet PC air bag DVD player air bag
Toner cartridges air bag LCD TV air bagMobile phone air bagluggage air bag
22. Product arrived
Need to use DLS charge
pressure range of the
product
Need to use clean
air source.
Specifications Air
pressure ( Mpa )
2 ㎝ air
column
0.07-0.09
3 ㎝ air
column
0.06-0.08
4 ㎝ air
column
0.05-0.07
6 ㎝ air 0.04-0.06
充气压力使用要求
Provide automated
assembly line
production
integration scheme
Provide automated
assembly line
production
integration scheme
Without complex pneumatic
device.
Basic inflatable operation
platform, and packing can be
made
23. (Authorized) Ming and designed the monocular
No. Application number The name ofinvention Patent type
1 200520043307.6
O the mucosa rebuffed air three-dimensional bags
manufacturing method invention
2 200510027668.6
C since mucosa rebuffed air three-dimensional bags
manufacturing method invention
3 200510027665.2
Since the mucosa rebuffed air three-dimensional
packaging materials and its manufacturing method invention
4 200510027666.7
U from mucosa rebuffed air three-dimensional bags
manufacturing method invention
5 200510028292.0
Since the mucosa check air C bag packaging materials
and its manufacturing method invention
6 200510028293.5
Since the mucosa check air J type bag packaging
materials and its manufacturing method invention
7 200510028294.x
Since the mucosa check air U bag packaging materials
and its manufacturing method invention
8 200510028295.4
Since the mucosa check air packaging material flat pad
and its manufacturing method invention
24. (Authorized) directory listing on the patent for utility model
NO. Application number The name of invention Patent type
1 200520041559.5 A packaging structure since mucosa check the air For utility model
2 200520043307.6 O the mucosa rebuffed air three-dimensional packing bag For utility model
3 200520043308.0 C since mucosa rebuffed air three-dimensional packing bag For utility model
4 200520043305.7 Since the mucosal rebuffed air solid packing materials For utility model
5 200520043306.1 U from mucosa rebuffed air three-dimensional packing bag For utility model
6 200520043883.0 Since the mucosa check air C bag packaging materials For utility model
7 200520043884.5 Since the mucosa check air bag packaging materials J type For utility model
8 200520043885.x Since the mucosa bag U check air packaging materials For utility model
9 200520043886.4 Since the mucosa check air packaging materials flat pad For utility model
10 200820055268.5 A functional air cushion bag since the mucosa For utility model
11 200820056754.9 An enhanced air packaging device For utility model
12 200820060153.5 An air cushion packaging For utility model
13 200820056755.3 A modified air packaging device For utility model
14 200820055627.7
Reusable multi-functional three-dimensional sealing packaging
materials For utility model
25. (Authorized) directory listing on the patent for utility model
No. Application number The name of invention Patent type
15 200820158038.1 An inflatable cushion packaging device For utility model
16 200920070216.X A thickening air packaging device For utility model
17 200920072690.6 An air packaging device For utility model
18 200920077892.X Air packaging equipment with double buffering For utility model
19 200920070217.4 A liquid crystal display panels air packaging device For utility model
20 200920072689.3 Air packaging unit For utility model
21 200920207924.3 Is the lateral air valve air packaging devices For utility model
22 200920210018.9 A special air packaging device For utility model
23 200920077835.1 Improve valve air packaging equipment For utility model
24 200920077845.5 For larger objects, such as LED air packaging device For utility model
25 201020164964.7 A device to plug type air packaging For utility model
26 201020164973.6 A three-layer type air packaging device For utility model
27 201020691971.2 A five-story structure air bags For utility model
26.
27. AD : F Building,ShaSan Industrial Zone,Shajing
Town , Bao'an District , Shenzhen
Directly : 0755-29973505 0755-2997350506 0755-
2997350507
FAX : 0755-29795678
CONTACT : Vince Shen MOBILE : +8618620329810
Facebook:https://www.facebook.com/Dinglisheng/
Skype: tripod.technology
http://www.cnair-bag.com
http://www.sz-dls.com