Munters provides temporary humidity control services for pharmaceutical manufacturers to protect products from moisture during production, storage, and transport. Their dry air systems create extremely low moisture environments needed for manufacturing pharmaceutical powders, tablets, and capsules without quality loss or contamination. By analyzing client needs and engineering customized dehumidification solutions, Munters ensures precise control of humidity conditions for increased productivity, reduced costs, and improved product quality and shelf life in pharmaceutical facilities.
For more than 200 years, DuPont has been putting
science to work by creating sustainable solutions essential
to a better, safer, healthier life for people everywhere. One
of the areas in which safety and health are of paramount
importance is in cleanrooms and controlled environments.
DuPont understands your need to do everything possible
to improve productivity and reduce risk in your controlled
environment. The DuPont Controlled Environments
portfolio offers a comprehensive selection of single-use
cleanroom garments and accessories designed for use in
pharmaceutical, medical device, biotech and electronic
settings that require high standards for particle and
microbiological contamination control.
Indeed, DuPont™ Tyvek® garments have a long history
of use in cleanrooms due to their excellent barrier
to particles, microorganisms and non-hazardous liquids.
They offer an ideal balance of protection, durability,
comfort and contamination control. They are available
in many styles for different cleanroom and controlled
environment applications, and are packaged and certified
to meet local market requirements.
With the DuPont Controlled Environments offering, you
get the advantage of a wide range of proven, science-based
solutions that help keep your cleanroom environment
protected.
For more information please visit tyvek.co.uk/isoclean
Good Manufacturing Practices (GMP) ensure that products are consistently produced and controlled according to quality standards for their intended use. GMP requirements include clearly defined and validated manufacturing processes, qualified personnel, suitable premises and equipment, approved procedures and instructions, and record keeping. Facilities, equipment, and operations must be designed and maintained to minimize risks of contamination and ensure quality.
Application of Electrospun nanofibresin food industrysujayasree o.j
Electrospinning is a simple, versatile, and cost-effective technology which generates nano fibers with high surface area to volume ratio
Solution and processing parameters such as viscosity, molecular weight, concentration of the polymer, applied voltage, tip to collector distance, conductivity, etc. significantly affect the fiber morphology and by manipulation of these parameters one can get desired properties for specific application
Spun nano fibers are increasingly being used in a variety of applications such as, tissue engineering scaffolds, wound healing, drug delivery, immobilization of enzymes, as membrane in biosensors, protective clothing, cosmetics, affinity membranes, encapsulation of bioactive component, active packaging, filtration applications etc.
The document provides guidelines for GMP compliance related to premises, buildings, and facilities used for pharmaceutical manufacturing. It addresses requirements for design, construction, and maintenance of premises to minimize risks of contamination and ensure cleaning and maintenance. Specific areas covered include storage, production, quality control, and ancillary facilities. It also provides guidance on air handling, plumbing, lighting, sanitation, and other infrastructure.
The term intelligent involves an ON/OFF switching function on the package in response to changing external/internal stimuli, in order to communicate the product status to its consumers or endusers.The use of features of high added value that enhance the functionality of a product, notably mechanical, electronic and chemical features that improve safety and efficiency.
This document discusses contamination control in semiconductor fabrication. It identifies five major classes of contaminants: particles, metallic ions, chemicals, bacteria, and airborne molecular contaminants. Contamination can reduce device yield, affect performance and reliability. Sources of contamination include air, the production facility, cleanroom personnel, process water, chemicals, gases and static charge. The document describes techniques for maintaining cleanliness, such as cleanrooms, air filtration, garment protocols and chemical purification. It also outlines requirements for wafer cleaning and differences between front-end-of-line and back-end-of-line processing.
Dairy and meat processing plants cleaning by Geeta ChauhanGeeta12344
Cleaning and sanitation are important processes in meat and dairy food processing plants to control microbes and ensure food safety. Some key points:
1. Thorough cleaning is required before sanitization to remove dirt, soil and residues that can protect microbes. Factors like equipment design, food contact surfaces, water and air quality impact cleaning efficiency.
2. Common cleaning methods include using detergents with hot water, pressure and scrubbing. Foam and gel cleaners are also used as they adhere better.
3. After cleaning, surfaces are sanitized using physical methods like hot water or steam, or chemical sanitizers like chlorine to reduce microbes to safe levels. Cleaning-in-
For more than 200 years, DuPont has been putting
science to work by creating sustainable solutions essential
to a better, safer, healthier life for people everywhere. One
of the areas in which safety and health are of paramount
importance is in cleanrooms and controlled environments.
DuPont understands your need to do everything possible
to improve productivity and reduce risk in your controlled
environment. The DuPont Controlled Environments
portfolio offers a comprehensive selection of single-use
cleanroom garments and accessories designed for use in
pharmaceutical, medical device, biotech and electronic
settings that require high standards for particle and
microbiological contamination control.
Indeed, DuPont™ Tyvek® garments have a long history
of use in cleanrooms due to their excellent barrier
to particles, microorganisms and non-hazardous liquids.
They offer an ideal balance of protection, durability,
comfort and contamination control. They are available
in many styles for different cleanroom and controlled
environment applications, and are packaged and certified
to meet local market requirements.
With the DuPont Controlled Environments offering, you
get the advantage of a wide range of proven, science-based
solutions that help keep your cleanroom environment
protected.
For more information please visit tyvek.co.uk/isoclean
Good Manufacturing Practices (GMP) ensure that products are consistently produced and controlled according to quality standards for their intended use. GMP requirements include clearly defined and validated manufacturing processes, qualified personnel, suitable premises and equipment, approved procedures and instructions, and record keeping. Facilities, equipment, and operations must be designed and maintained to minimize risks of contamination and ensure quality.
Application of Electrospun nanofibresin food industrysujayasree o.j
Electrospinning is a simple, versatile, and cost-effective technology which generates nano fibers with high surface area to volume ratio
Solution and processing parameters such as viscosity, molecular weight, concentration of the polymer, applied voltage, tip to collector distance, conductivity, etc. significantly affect the fiber morphology and by manipulation of these parameters one can get desired properties for specific application
Spun nano fibers are increasingly being used in a variety of applications such as, tissue engineering scaffolds, wound healing, drug delivery, immobilization of enzymes, as membrane in biosensors, protective clothing, cosmetics, affinity membranes, encapsulation of bioactive component, active packaging, filtration applications etc.
The document provides guidelines for GMP compliance related to premises, buildings, and facilities used for pharmaceutical manufacturing. It addresses requirements for design, construction, and maintenance of premises to minimize risks of contamination and ensure cleaning and maintenance. Specific areas covered include storage, production, quality control, and ancillary facilities. It also provides guidance on air handling, plumbing, lighting, sanitation, and other infrastructure.
The term intelligent involves an ON/OFF switching function on the package in response to changing external/internal stimuli, in order to communicate the product status to its consumers or endusers.The use of features of high added value that enhance the functionality of a product, notably mechanical, electronic and chemical features that improve safety and efficiency.
This document discusses contamination control in semiconductor fabrication. It identifies five major classes of contaminants: particles, metallic ions, chemicals, bacteria, and airborne molecular contaminants. Contamination can reduce device yield, affect performance and reliability. Sources of contamination include air, the production facility, cleanroom personnel, process water, chemicals, gases and static charge. The document describes techniques for maintaining cleanliness, such as cleanrooms, air filtration, garment protocols and chemical purification. It also outlines requirements for wafer cleaning and differences between front-end-of-line and back-end-of-line processing.
Dairy and meat processing plants cleaning by Geeta ChauhanGeeta12344
Cleaning and sanitation are important processes in meat and dairy food processing plants to control microbes and ensure food safety. Some key points:
1. Thorough cleaning is required before sanitization to remove dirt, soil and residues that can protect microbes. Factors like equipment design, food contact surfaces, water and air quality impact cleaning efficiency.
2. Common cleaning methods include using detergents with hot water, pressure and scrubbing. Foam and gel cleaners are also used as they adhere better.
3. After cleaning, surfaces are sanitized using physical methods like hot water or steam, or chemical sanitizers like chlorine to reduce microbes to safe levels. Cleaning-in-
This document discusses microbial contamination control in parenteral manufacturing. It outlines various layers of protection used, including terminal sterilization techniques like autoclaving. It also discusses aseptic processing and sources of contamination control strategies during aseptic manufacture. Other topics covered include blow-fill-seal technology, issues in sterilization by filtration, sterile prefilled syringes, process validation, hazard analysis and critical control points. Key sterilization techniques and the selection of appropriate test organisms to validate these processes are also summarized.
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.
A dehumidifier is a machine that removes excess moisture from the air. An industrial dehumidifier is built to be transported and used in several hard-wearing locations.
Commercial and industrial dehumidifiers will reduce mold, condensation dripping from pipes or windows, and eliminate musty smells.
This document provides an overview of GMP manufacturing environments. It discusses that the manufacturing environment is critical for product quality and outlines factors that must be controlled, such as temperature, humidity, air cleanliness, and room pressure. It defines contamination and cross-contamination, and explains how cleanrooms are classified based on particle and bacterial limits. The document also discusses how air handling systems, clothing, and procedures influence the level of protection required in different zones of a pharmaceutical facility.
This document discusses utilities and HVAC systems used in pharmaceutical manufacturing facilities. It provides details on various utility services including HVAC, plumbing, drainage, gas, sanitation, water, and fire protection systems. It describes the functions of heating, ventilation, air conditioning, temperature and humidity control, air filtration and flow, and other components of HVAC systems. It emphasizes the critical roles of utilities and HVAC in maintaining environmental controls for sterile and contamination-sensitive areas in pharmaceutical facilities.
Industrial Steam Cleaners for Equipment Maintenance: An OverviewPure Steam Cleaners
In the industrial sector, equipment maintenance is a critical aspect that ensures smooth operations and maximises the lifespan of machinery. Over time, industrial equipment can accumulate dirt, grime, and other contaminants, which can affect its performance and efficiency. To tackle these challenges, industrial steam cleaners have emerged as a reliable and efficient solution for equipment maintenance. In this article, we will delve into the world of Industrial steam cleaners for equipment maintenance and explore their applications, benefits, and considerations for effective use.
This document provides guidelines on heating, ventilation and air conditioning (HVAC) systems for manufacturing solid dosage pharmaceutical products. It discusses HVAC system design considerations to protect products, personnel and the environment. Key recommendations include ensuring HVAC systems provide appropriate temperature, humidity and air quality during manufacturing and storage. HVAC systems should be designed at the concept stage and qualified to demonstrate they will perform as intended. The guidelines are meant to complement good manufacturing practice standards.
This document discusses the infrastructure requirements for manufacturing lithium ion batteries, including dehumidifiers. It explains that battery production requires strictly controlled ultra-low humidity levels below 1% RH. Desiccant dehumidification systems are needed to maintain dry rooms at -40 to -50°C dew point to control humidity and temperature. The document provides details on dry room layouts, dehumidifier designs, clean room standards, and manufacturing processes that require precise climate control to optimize battery quality and performance.
Indoor air quality is important for health and comfort. This document discusses indoor air quality standards and guidelines from organizations like ASHRAE. It outlines maximum recommended levels of contaminants like carbon dioxide and particulate matter. Maintaining good indoor air quality involves controlling sources of contamination, proper ventilation, humidity management, and adequate filtration of indoor air. Key aspects of a good ventilation system include cleanable components, accessibility for maintenance, and managing both indoor and outdoor air quality.
The document outlines 11 principles of sanitary facility design for food production facilities. The principles establish distinct hygienic zones; control personnel and material flows to reduce hazards; and control water accumulations, temperature, humidity, airflow, and air quality. Additional principles address site elements, building envelopes, interior spatial design, building components, utility systems design, and integrating sanitation into the overall facility design. Thorough cleaning and sanitation are critical to maintaining food safety and quality.
This document provides guidelines for facilities that handle pharmaceutical products containing hazardous substances. It discusses risk assessments to determine appropriate safety measures and describes requirements for facility layout, air handling systems, environmental protection, and personal protective equipment. The key areas covered are ensuring quality of products while protecting operators and the environment from hazardous materials through adequate facility design, ventilation, containment, and PPE use. Risk assessments should determine the necessary controls based on the potential hazards. Facilities should be designed to prevent contamination and exposure through features like airlocks, pressure differentials, and clearly delineated material and personnel flow paths.
Paper ewea 2013 the use of a large climate chamber for extreme temperature te...Pieter Jan Jordaens
The document discusses the use of a large climate chamber for testing wind turbine components under extreme temperatures. It describes how components need to withstand temperatures from -60°C to +60°C in remote locations. The climate chamber at OWI-Lab can test components up to 150 tonnes in this wide temperature range to improve reliability. Testing helps reduce maintenance costs and avoid failures by validating designs under harsh conditions.
Benefits of Industrial Steam Cleaners in Dairy ProductionPure Steam Cleaners
Industrial steam cleaners have revolutionised the dairy industry, offering a plethora of advantages that traditional cleaning methods simply cannot match. In today’s fast-paced dairy production environment, ensuring cleanliness is paramount. Industrial steam cleaners have emerged as a game-changer, providing efficient, eco-friendly, and thorough cleaning solutions. In this article, we’ll explore the multiple benefits these innovative machines bring to the table, making them indispensable in the world of dairy production.
Integrated pest management excludes pests from food manufacturing and storage facilities by effective and well-maintained physical and alternate barriers. Learn more on the topics along with weekly buzz and highlights on the F&B industry in this weeks PMG Tech-knowledge.
Aquafeed producers are losing about $4 to $10 per ton of product produced in terms of lost production, higher energy consumption and lowered product quality. These losses can be recovered by substituting a more effective moisture (MC) sensing and control technology for currently used traditional MC sensing and control.
Natgraph manufactures a range of modular air force dryers for drying coatings applied to various materials. The dryers use high velocity heated air to dry substrates quickly and efficiently while remaining economical to operate. The dryers come in standard belt widths and can be customized with options like extended inlets/outlets, CCTV systems, and various paint finishes. Touch screen controls allow for monitoring and adjustment of drying conditions.
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This document discusses microbial contamination control in parenteral manufacturing. It outlines various layers of protection used, including terminal sterilization techniques like autoclaving. It also discusses aseptic processing and sources of contamination control strategies during aseptic manufacture. Other topics covered include blow-fill-seal technology, issues in sterilization by filtration, sterile prefilled syringes, process validation, hazard analysis and critical control points. Key sterilization techniques and the selection of appropriate test organisms to validate these processes are also summarized.
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.
A dehumidifier is a machine that removes excess moisture from the air. An industrial dehumidifier is built to be transported and used in several hard-wearing locations.
Commercial and industrial dehumidifiers will reduce mold, condensation dripping from pipes or windows, and eliminate musty smells.
This document provides an overview of GMP manufacturing environments. It discusses that the manufacturing environment is critical for product quality and outlines factors that must be controlled, such as temperature, humidity, air cleanliness, and room pressure. It defines contamination and cross-contamination, and explains how cleanrooms are classified based on particle and bacterial limits. The document also discusses how air handling systems, clothing, and procedures influence the level of protection required in different zones of a pharmaceutical facility.
This document discusses utilities and HVAC systems used in pharmaceutical manufacturing facilities. It provides details on various utility services including HVAC, plumbing, drainage, gas, sanitation, water, and fire protection systems. It describes the functions of heating, ventilation, air conditioning, temperature and humidity control, air filtration and flow, and other components of HVAC systems. It emphasizes the critical roles of utilities and HVAC in maintaining environmental controls for sterile and contamination-sensitive areas in pharmaceutical facilities.
Industrial Steam Cleaners for Equipment Maintenance: An OverviewPure Steam Cleaners
In the industrial sector, equipment maintenance is a critical aspect that ensures smooth operations and maximises the lifespan of machinery. Over time, industrial equipment can accumulate dirt, grime, and other contaminants, which can affect its performance and efficiency. To tackle these challenges, industrial steam cleaners have emerged as a reliable and efficient solution for equipment maintenance. In this article, we will delve into the world of Industrial steam cleaners for equipment maintenance and explore their applications, benefits, and considerations for effective use.
This document provides guidelines on heating, ventilation and air conditioning (HVAC) systems for manufacturing solid dosage pharmaceutical products. It discusses HVAC system design considerations to protect products, personnel and the environment. Key recommendations include ensuring HVAC systems provide appropriate temperature, humidity and air quality during manufacturing and storage. HVAC systems should be designed at the concept stage and qualified to demonstrate they will perform as intended. The guidelines are meant to complement good manufacturing practice standards.
This document discusses the infrastructure requirements for manufacturing lithium ion batteries, including dehumidifiers. It explains that battery production requires strictly controlled ultra-low humidity levels below 1% RH. Desiccant dehumidification systems are needed to maintain dry rooms at -40 to -50°C dew point to control humidity and temperature. The document provides details on dry room layouts, dehumidifier designs, clean room standards, and manufacturing processes that require precise climate control to optimize battery quality and performance.
Indoor air quality is important for health and comfort. This document discusses indoor air quality standards and guidelines from organizations like ASHRAE. It outlines maximum recommended levels of contaminants like carbon dioxide and particulate matter. Maintaining good indoor air quality involves controlling sources of contamination, proper ventilation, humidity management, and adequate filtration of indoor air. Key aspects of a good ventilation system include cleanable components, accessibility for maintenance, and managing both indoor and outdoor air quality.
The document outlines 11 principles of sanitary facility design for food production facilities. The principles establish distinct hygienic zones; control personnel and material flows to reduce hazards; and control water accumulations, temperature, humidity, airflow, and air quality. Additional principles address site elements, building envelopes, interior spatial design, building components, utility systems design, and integrating sanitation into the overall facility design. Thorough cleaning and sanitation are critical to maintaining food safety and quality.
This document provides guidelines for facilities that handle pharmaceutical products containing hazardous substances. It discusses risk assessments to determine appropriate safety measures and describes requirements for facility layout, air handling systems, environmental protection, and personal protective equipment. The key areas covered are ensuring quality of products while protecting operators and the environment from hazardous materials through adequate facility design, ventilation, containment, and PPE use. Risk assessments should determine the necessary controls based on the potential hazards. Facilities should be designed to prevent contamination and exposure through features like airlocks, pressure differentials, and clearly delineated material and personnel flow paths.
Paper ewea 2013 the use of a large climate chamber for extreme temperature te...Pieter Jan Jordaens
The document discusses the use of a large climate chamber for testing wind turbine components under extreme temperatures. It describes how components need to withstand temperatures from -60°C to +60°C in remote locations. The climate chamber at OWI-Lab can test components up to 150 tonnes in this wide temperature range to improve reliability. Testing helps reduce maintenance costs and avoid failures by validating designs under harsh conditions.
Benefits of Industrial Steam Cleaners in Dairy ProductionPure Steam Cleaners
Industrial steam cleaners have revolutionised the dairy industry, offering a plethora of advantages that traditional cleaning methods simply cannot match. In today’s fast-paced dairy production environment, ensuring cleanliness is paramount. Industrial steam cleaners have emerged as a game-changer, providing efficient, eco-friendly, and thorough cleaning solutions. In this article, we’ll explore the multiple benefits these innovative machines bring to the table, making them indispensable in the world of dairy production.
Integrated pest management excludes pests from food manufacturing and storage facilities by effective and well-maintained physical and alternate barriers. Learn more on the topics along with weekly buzz and highlights on the F&B industry in this weeks PMG Tech-knowledge.
Aquafeed producers are losing about $4 to $10 per ton of product produced in terms of lost production, higher energy consumption and lowered product quality. These losses can be recovered by substituting a more effective moisture (MC) sensing and control technology for currently used traditional MC sensing and control.
Natgraph manufactures a range of modular air force dryers for drying coatings applied to various materials. The dryers use high velocity heated air to dry substrates quickly and efficiently while remaining economical to operate. The dryers come in standard belt widths and can be customized with options like extended inlets/outlets, CCTV systems, and various paint finishes. Touch screen controls allow for monitoring and adjustment of drying conditions.
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Unlocking WhatsApp Marketing with HubSpot: Integrating Messaging into Your Ma...Niswey
50 million companies worldwide leverage WhatsApp as a key marketing channel. You may have considered adding it to your marketing mix, or probably already driving impressive conversions with WhatsApp.
But wait. What happens when you fully integrate your WhatsApp campaigns with HubSpot?
That's exactly what we explored in this session.
We take a look at everything that you need to know in order to deploy effective WhatsApp marketing strategies, and integrate it with your buyer journey in HubSpot. From technical requirements to innovative campaign strategies, to advanced campaign reporting - we discuss all that and more, to leverage WhatsApp for maximum impact. Check out more details about the event here https://events.hubspot.com/events/details/hubspot-new-delhi-presents-unlocking-whatsapp-marketing-with-hubspot-integrating-messaging-into-your-marketing-strategy/
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Revolutionizing Surface Protection Xlcoatings Nano Based SolutionsExcel coatings
Excelcoating Transforming surface protection with their cutting-edge, eco-friendly nano-based coatings. This presentation delves into their innovative product lineup, including Excel CoolCoat for roof cooling, Excel NanoSeal for cement surfaces, Excel StayCool for UV-filtering glass, Excel StayClean for solar panels, Excel CoolTile for heat-reflective tiles, and Excel InsulX for film insulation.
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L'indice de performance des ports à conteneurs de l'année 2023SPATPortToamasina
Une évaluation comparable de la performance basée sur le temps d'escale des navires
L'objectif de l'ICPP est d'identifier les domaines d'amélioration qui peuvent en fin de compte bénéficier à toutes les parties concernées, des compagnies maritimes aux gouvernements nationaux en passant par les consommateurs. Il est conçu pour servir de point de référence aux principaux acteurs de l'économie mondiale, notamment les autorités et les opérateurs portuaires, les gouvernements nationaux, les organisations supranationales, les agences de développement, les divers intérêts maritimes et d'autres acteurs publics et privés du commerce, de la logistique et des services de la chaîne d'approvisionnement.
Le développement de l'ICPP repose sur le temps total passé par les porte-conteneurs dans les ports, de la manière expliquée dans les sections suivantes du rapport, et comme dans les itérations précédentes de l'ICPP. Cette quatrième itération utilise des données pour l'année civile complète 2023. Elle poursuit le changement introduit l'année dernière en n'incluant que les ports qui ont eu un minimum de 24 escales valides au cours de la période de 12 mois de l'étude. Le nombre de ports inclus dans l'ICPP 2023 est de 405.
Comme dans les éditions précédentes de l'ICPP, la production du classement fait appel à deux approches méthodologiques différentes : une approche administrative, ou technique, une méthodologie pragmatique reflétant les connaissances et le jugement des experts ; et une approche statistique, utilisant l'analyse factorielle (AF), ou plus précisément la factorisation matricielle. L'utilisation de ces deux approches vise à garantir que le classement des performances des ports à conteneurs reflète le plus fidèlement possible les performances réelles des ports, tout en étant statistiquement robuste.
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Discover the Beauty and Functionality of The Expert Remodeling Serviceobriengroupinc04
Unlock your kitchen's true potential with expert remodeling services from O'Brien Group Inc. Transform your space into a functional, modern, and luxurious haven with their experienced professionals. From layout reconfiguration to high-end upgrades, they deliver stunning results tailored to your style and needs. Visit obriengroupinc.com to elevate your kitchen's beauty and functionality today.
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1. Pharmaceutical
INDUSTRIAL
Property Damage Temporary Property Performance
Restoration Humidity Control Services
ApplicAtiOn
Overview Temporary humidity control is necessary
during periods of the year when air moisture
Munters Temporary Humidity Control Services provides content is at its highest. The most effective
way to protect raw materials and products
a solution for manufacturers of pharmaceutical products
during production, storage and transport is
within the health care market. Pharmaceutical products to control the surrounding environment.
such as powders, tablets and capsules often lose The Munters dry air system is the simplest,
most cost effective way of achieving and
quality and shelf life when they come into contact with
controlling humidity conditions during production.
moisture in the air. Moist air also contains bacteria
which can increase the potential of contamination in Many pharmaceutical products need to be
produced and packed in an environment
production and storage. In a dry environment, bacterial which demands extremely low moisture
growth is inhibited. content. The temporary dehumidification
systems can create a climate that reduces
When hygroscopic ingredients and powders absorb moisture levels to a point where products
moisture they become sticky and build up inside the can be manufactured without any loss of
quality, while providing consistent dry air
conveying lines. This slows the packaging process, at the specified dew-point.
creates sanitation concerns and eventually causes
Munters can provide custom-designed
costly downtime.
dehumidification solutions for all areas
of production including silos, production
facilities, packaging, storage and transport.
The temporary climate control equipment
comprises desiccant dehumidifiers, cooling
and heating equipment, which has been
designed to help meet the specifications
and needs of the contractors, owners
and engineers.
controlling the pharmaceutical process.
www.munters.com/mcs
2. Pharmaceutical
INDUSTRIAL
prOcedure
In order to ensure that the equipment is
tailored specifically to each environment,
the following information is required:
• Size of the room
• Ventilation rate
• Moisture load from product
• Heat load from equipment
• Room material
• Infiltration rate.
Only when this information is compiled Many pharmaceutical products need to be pharmaceutical production area.
and analysed can the suitable equipment produced and packed in an environment,
which demands extremely low moisture content.
be selected. Munters personnel then
engineer the equipment for specific
applications to meet the desired results BeneFits
specifications and avoid contamination.
The use of a dehumidification system is The Munters dry air system is the
Munters technicians’ service and check
a simple and effective way to combat simplest, most precise way of
the equipment, ducting and ancillary
humidity problems in a pharmaceutical achieving and controlling the humidity
items prior to delivery. It is vital that
facility. The result is higher productivity, conditions required, including:
the dehumidifier is sanitised and the
reduced production costs, less down time
ducting is new to eliminate the threat • Considerable energy cost savings,
and higher product quality.
of contamination. The equipment is then incorporating environmentally-
placed in a designated area, positioned friendly technology
close to a power supply and set up to • Improved hygiene conditions
maximise the safe operation of the unit.
• Increased product quality and
Munters state-of-the-art desiccant shelf life
dehumidification systems are utilised to • Consistent production, all year
deep dry the ambient air in the facility around with the elimination of
which ensures that moisture sensitive delays due to high moisture levels
products being manufactured are
• Improved production increases
processed in the optimum environment.
of 15-20%
Munters provides a turnkey solution
with well engineered equipment, offering • Shorter drying times for
an around the clock service that is coated products
unmatched in the industry.
• Compliance with Good Manufacturing
Practice (GMP) regulations
• Allows the client to work around
the clock
• A rental program that allows the
customer to only use the equipment
in production. when it is actually required.
THC35/05/08
www.munters.com/mcs