Bovine Leukosis Virus: What is it and What Does it Mean for Me?DAIReXNET
Dr. Ray Sweeney presented this material for DAIReXNET on October 14, 2015. To view the full presentation, please see our archived webinars page at http://www.extension.org/pages/15830/archived-dairy-cattle-webinars
Practical Power Quality Measurements and Fixes Presented by Fluke and TranscatTranscat
This webinar explores the following:
-The first clues of a problem
-Approaching the problem
-Equipment setup
-Which measurement to make
-Analyzing the data
-Fixing the problem
Validation of lab instruments and quantitative test methods Mostafa Mahmoud
This lecture shows the procedures applied when going to validate your laboratory instruments and quantitative test methods also either FDA approved or laboratory developed tests.
Quality control, or QC for short, is a process by which entities review the quality of all factors involved in the production. ISO 9000 defines quality control as "A part of quality management focused on fulfilling quality requirements"
This presentation gives a brief idea of Quality control and how to execute it.
Presentation by Michael Healy, Student Intern from Sydney University at the Milton Pink Eye Workshop held on the 18th June 2009. This Presentation covers:
- What is Bovine Viral Diarrhoea (BVDV) or Pertivirus
- Case Study on a South Coast Diary Herd
- Control Methods
Bovine Leukosis Virus: What is it and What Does it Mean for Me?DAIReXNET
Dr. Ray Sweeney presented this material for DAIReXNET on October 14, 2015. To view the full presentation, please see our archived webinars page at http://www.extension.org/pages/15830/archived-dairy-cattle-webinars
Practical Power Quality Measurements and Fixes Presented by Fluke and TranscatTranscat
This webinar explores the following:
-The first clues of a problem
-Approaching the problem
-Equipment setup
-Which measurement to make
-Analyzing the data
-Fixing the problem
Validation of lab instruments and quantitative test methods Mostafa Mahmoud
This lecture shows the procedures applied when going to validate your laboratory instruments and quantitative test methods also either FDA approved or laboratory developed tests.
Quality control, or QC for short, is a process by which entities review the quality of all factors involved in the production. ISO 9000 defines quality control as "A part of quality management focused on fulfilling quality requirements"
This presentation gives a brief idea of Quality control and how to execute it.
Presentation by Michael Healy, Student Intern from Sydney University at the Milton Pink Eye Workshop held on the 18th June 2009. This Presentation covers:
- What is Bovine Viral Diarrhoea (BVDV) or Pertivirus
- Case Study on a South Coast Diary Herd
- Control Methods
Use of rapid quality control test methods as alternatives to traditional meth...Merck Life Sciences
Abstract:
As the market for advanced therapy medicinal products (ATMP) matures the complexities of these molecules are evident and challenging when routine standard quality control (QC) testing is applied. Short shelf life from the point of manufacture to administration to the patient results in relatively low volumes for small scale clinical trials or small patient populations. Within a limited time period and with this low product volume, it is necessary to complete required regulatory QC testing, be that for early or late phase clinical trials, or for licensed drug product in a reduced timescale. So, the challenges with QC testing of cell and gene therapies using traditional test methods is time to results, due to short shelf-life, and availability of sufficient sample, due to low production volumes. Over the past years the application of rapid testing of short-life cell and gene therapies that may also help conserve limited product availability have been utilised. Regulatory expectations for using rapid test methods in place of classical or compendial test methods have been defined and this presentation will provide examples and data from our own experience of a range of alternate methods for application to ATMP products.
Quality in clinical laboratory is a continuous journey of improving processes through team work, innovative solutions, regulatory compliance with final objective to meet the evolving needs of clinicians & patients.
Parvovirus Filtration Best Practices - 25 Years of Hands-On ExperienceMerck Life Sciences
In this webinar, you will learn:
- how to measure filter performance and capacity,
- how to optimize filter virus removal capability,
- and avoid potential pit-falls
Detailed description:
This webinar will cover all aspects of parvovirus filtration best practices: process development/ optimization, pilot scale-up, and validation and explain the important connections between these activities. The rationale for the recommended best practices will be explained by discussing the underlying mechanisms that control filter performance.
Process development guidance for AAV and lentivirus manufacturing based on co...MilliporeSigma
Access the interactive recording here: https://bit.ly/37nl3Ex
Webinar summary:
An efficient production platform is essential for successful commercial implementation of gene therapy programs. AAV and Lentivirus manufacturing process are often developed with compressed timelines, reduced process optimization and low product yields which can have significant effect on costs.
In this webinar, you will learn:
* How manufacturing costs are examined for adeno-associated virus and lentivirus production with several different for each vector
* That key process characteristics like production titer, production of empty viral particles, downstream product recovery, and the batching strategy can effect the overall manufacturing cost
* How holistic evaluation is an important tool during process development to help prioritize different approaches to improve viral vector production processes
Abstract:
An efficient production platform is essential for successful commercial implementation of gene therapy programs. Viral vector manufacturing processes are often developed under timelines which are considerably shorter than those for more mature biopharmaceuticals. Consequently, the level of process optimization is reduced and challenges related to low product yields are common. These factors, as well as the small batch sizes common for these processes, can have significant effect on manufacturing costs.
Validation of Tangential Flow Filtration in Biotech ProcessesMerck Life Sciences
Watch the presentation of this webinar here: https://bit.ly/3hUKfd7
The objective of validation of a unit operation is to demonstrate with a high degree of confidence that the process performs consistently. The present seminar will focus on the validation of the unit operation of TFF and will provide an overview of the regulatory landscape, the validation master plan, approaches to membrane re-use, cleaning validation, and best practices.
In this webinar, you will learn:
• Validation of TFF
• Validation master plan
• Membrane reuse and cleaning
• TFF scale down models
Speaker: Dr. Subhasis Banerjee,
Principal Technical Application Expert, Bioprocessing APAC
This manual "CFC for S7" provides you with the information you require to use the
CFC configuration tool in conjunction with CPUs in SIMATIC S7 programmable
controllers (PLCs).
Developing a single use adenovirus-vectored vaccine process through public-pr...Merck Life Sciences
This work highlights the importance of collaborations to accelerate vaccine process development and manufacturing under the constant pressure of emerging diseases and the growing need of global immunizations.
We are collaborating with the Jenner Institute of the University of Oxford to advance the development of a rapid, scalable and GMP compliant process for simian adenoviruses used as vector for vaccines such as Rabies and emerging threats like Zika and Ebola. This webinar will describe the transition from a labor and time intensive process development to one utilizing a maximum of disposable technologies such as single use bioreactors and filtration technologies, using the rabies vaccine as a first candidate. We will highlight the challenges and their corresponding solutions that in the end created a template that can be used for different types of adenoviral vectors-based vaccines manufacturing.
In this webinar, you will learn:
- The challenges of creating a rapid and scalable process for Adenovirus vector manufacturing.
- The solutions that overcame those challenges.
- How public-private collaborations can accelerate vaccine process development.
As information technology continues to open new pathways in clinical diagnostics and broaden how we measure and define success, lab directors must consider how IT can complement their investment in automation. In fact, automation and IT systems can no longer be regarded as separate laboratory solutions, but rather must be viewed as a single entity that exists to maximize input and output across the laboratory continuum. With automation serving to centralize testing and tube throughput and IT to aggregate and display testing data quickly and accurately, the benefits of the whole clearly become more important than the sum of its parts.
That is why it is paramount to research the availability and capabilities of an IT system that can enhance an automation solution. When automation and IT functionality combine, the closed-system loop provides seamless, total process management at a magnitude far greater than can be achieved by an automation solution that lacks adequate IT support.
Dr. Paul Thomas - Porcine Epidemic Diarrhea Virus (PEDv)John Blue
Porcine Epidemic Diarrhea Virus (PEDv) - Dr. Paul Thomas, AMVC, LLC, from the 2015 World Pork Expo, June 3 - 5, 2015, Des Moines, IA, USA.
More presentations at http://www.swinecast.com/2015-world-pork-expo
Sterilization Validation for Medical DevicesDocKetchum
Every medical device produced must be sterilized before being shipped to hospitals, doctors’ offices, and other medical locations.
Random samples of these devices must then be tested to be sure the sterilization kills disease causing microbes including bacteria, fungus, and spores in every device.
These are some of the most common ways that sterilization validation is performed.
Internal quality control (IQC) in coagulation labAnkit Raiyani
In the haematology laboratory it is essential to ensure that the right test is carried out on the right specimen and that the correct results are delivered to the appropriate recipient without delay.
Quality control (QC) is defined as measures that must be included during each assay run to verify that the test is working properly.
Internal quality control (IQC) is monitoring the haematology test procedures to ensure continual evaluation of the reliability of the daily work of the laboratory with validation of tests before reports are released
Global #1 leader in X-ray inspections. Top Checkweighers since 1964 over 100,000! Top unique multi-frequency Metal Detectors. Top Integrated Combos. Chicago assembly, SoCal technicians. www.anritsu.com/infivis
Use of rapid quality control test methods as alternatives to traditional meth...Merck Life Sciences
Abstract:
As the market for advanced therapy medicinal products (ATMP) matures the complexities of these molecules are evident and challenging when routine standard quality control (QC) testing is applied. Short shelf life from the point of manufacture to administration to the patient results in relatively low volumes for small scale clinical trials or small patient populations. Within a limited time period and with this low product volume, it is necessary to complete required regulatory QC testing, be that for early or late phase clinical trials, or for licensed drug product in a reduced timescale. So, the challenges with QC testing of cell and gene therapies using traditional test methods is time to results, due to short shelf-life, and availability of sufficient sample, due to low production volumes. Over the past years the application of rapid testing of short-life cell and gene therapies that may also help conserve limited product availability have been utilised. Regulatory expectations for using rapid test methods in place of classical or compendial test methods have been defined and this presentation will provide examples and data from our own experience of a range of alternate methods for application to ATMP products.
Quality in clinical laboratory is a continuous journey of improving processes through team work, innovative solutions, regulatory compliance with final objective to meet the evolving needs of clinicians & patients.
Parvovirus Filtration Best Practices - 25 Years of Hands-On ExperienceMerck Life Sciences
In this webinar, you will learn:
- how to measure filter performance and capacity,
- how to optimize filter virus removal capability,
- and avoid potential pit-falls
Detailed description:
This webinar will cover all aspects of parvovirus filtration best practices: process development/ optimization, pilot scale-up, and validation and explain the important connections between these activities. The rationale for the recommended best practices will be explained by discussing the underlying mechanisms that control filter performance.
Process development guidance for AAV and lentivirus manufacturing based on co...MilliporeSigma
Access the interactive recording here: https://bit.ly/37nl3Ex
Webinar summary:
An efficient production platform is essential for successful commercial implementation of gene therapy programs. AAV and Lentivirus manufacturing process are often developed with compressed timelines, reduced process optimization and low product yields which can have significant effect on costs.
In this webinar, you will learn:
* How manufacturing costs are examined for adeno-associated virus and lentivirus production with several different for each vector
* That key process characteristics like production titer, production of empty viral particles, downstream product recovery, and the batching strategy can effect the overall manufacturing cost
* How holistic evaluation is an important tool during process development to help prioritize different approaches to improve viral vector production processes
Abstract:
An efficient production platform is essential for successful commercial implementation of gene therapy programs. Viral vector manufacturing processes are often developed under timelines which are considerably shorter than those for more mature biopharmaceuticals. Consequently, the level of process optimization is reduced and challenges related to low product yields are common. These factors, as well as the small batch sizes common for these processes, can have significant effect on manufacturing costs.
Validation of Tangential Flow Filtration in Biotech ProcessesMerck Life Sciences
Watch the presentation of this webinar here: https://bit.ly/3hUKfd7
The objective of validation of a unit operation is to demonstrate with a high degree of confidence that the process performs consistently. The present seminar will focus on the validation of the unit operation of TFF and will provide an overview of the regulatory landscape, the validation master plan, approaches to membrane re-use, cleaning validation, and best practices.
In this webinar, you will learn:
• Validation of TFF
• Validation master plan
• Membrane reuse and cleaning
• TFF scale down models
Speaker: Dr. Subhasis Banerjee,
Principal Technical Application Expert, Bioprocessing APAC
This manual "CFC for S7" provides you with the information you require to use the
CFC configuration tool in conjunction with CPUs in SIMATIC S7 programmable
controllers (PLCs).
Developing a single use adenovirus-vectored vaccine process through public-pr...Merck Life Sciences
This work highlights the importance of collaborations to accelerate vaccine process development and manufacturing under the constant pressure of emerging diseases and the growing need of global immunizations.
We are collaborating with the Jenner Institute of the University of Oxford to advance the development of a rapid, scalable and GMP compliant process for simian adenoviruses used as vector for vaccines such as Rabies and emerging threats like Zika and Ebola. This webinar will describe the transition from a labor and time intensive process development to one utilizing a maximum of disposable technologies such as single use bioreactors and filtration technologies, using the rabies vaccine as a first candidate. We will highlight the challenges and their corresponding solutions that in the end created a template that can be used for different types of adenoviral vectors-based vaccines manufacturing.
In this webinar, you will learn:
- The challenges of creating a rapid and scalable process for Adenovirus vector manufacturing.
- The solutions that overcame those challenges.
- How public-private collaborations can accelerate vaccine process development.
As information technology continues to open new pathways in clinical diagnostics and broaden how we measure and define success, lab directors must consider how IT can complement their investment in automation. In fact, automation and IT systems can no longer be regarded as separate laboratory solutions, but rather must be viewed as a single entity that exists to maximize input and output across the laboratory continuum. With automation serving to centralize testing and tube throughput and IT to aggregate and display testing data quickly and accurately, the benefits of the whole clearly become more important than the sum of its parts.
That is why it is paramount to research the availability and capabilities of an IT system that can enhance an automation solution. When automation and IT functionality combine, the closed-system loop provides seamless, total process management at a magnitude far greater than can be achieved by an automation solution that lacks adequate IT support.
Dr. Paul Thomas - Porcine Epidemic Diarrhea Virus (PEDv)John Blue
Porcine Epidemic Diarrhea Virus (PEDv) - Dr. Paul Thomas, AMVC, LLC, from the 2015 World Pork Expo, June 3 - 5, 2015, Des Moines, IA, USA.
More presentations at http://www.swinecast.com/2015-world-pork-expo
Sterilization Validation for Medical DevicesDocKetchum
Every medical device produced must be sterilized before being shipped to hospitals, doctors’ offices, and other medical locations.
Random samples of these devices must then be tested to be sure the sterilization kills disease causing microbes including bacteria, fungus, and spores in every device.
These are some of the most common ways that sterilization validation is performed.
Internal quality control (IQC) in coagulation labAnkit Raiyani
In the haematology laboratory it is essential to ensure that the right test is carried out on the right specimen and that the correct results are delivered to the appropriate recipient without delay.
Quality control (QC) is defined as measures that must be included during each assay run to verify that the test is working properly.
Internal quality control (IQC) is monitoring the haematology test procedures to ensure continual evaluation of the reliability of the daily work of the laboratory with validation of tests before reports are released
Global #1 leader in X-ray inspections. Top Checkweighers since 1964 over 100,000! Top unique multi-frequency Metal Detectors. Top Integrated Combos. Chicago assembly, SoCal technicians. www.anritsu.com/infivis
Modular systems for precision oxygen analysis
of packaging film barriers. Systech Illinois 8000 Series analysers offer the widest measurement range in the market.
Draeger X-act 7000 lets you precisely measure gases in the low parts per billion (ppb) range on site. It's easy to use, simply insert the Draeger MicroTubes, begin measuring, results are displayed on the display. Gas detectable are Benzene, 1,3 Butadiene, Ethylene Oxide, Formaldehyde & finally Mercury for the first time.
Esco Containment Barrier Isolator (CBI) facilitates the isolation of a product or process while providing the required conditions for a sterile/ aseptic environment. It is configured to operate at positive or negative pressure. This equipment provides a comprehensive range of personnel
and product protection in addition to protection for the surrounding work areas and the environment.
CBI's design has complete compliance to PIC/s and EU cGMP standardswith its 19 mm radius coved internal corners in a single piece chamber (no perforations or grilles for contaminants to be trapped on all 4 corners). Its Rear Return Filter ensures that ducts are not contaminated. The system comes in either recirculatory or single pass airflow.
Applications
• Pharmacy Compounding (Chemotherapy/TPN)
• As a Class III Cabinet for Biosafety Levels (BSL) 3 and 4
• Small Batch Sterility Testing
• Small-scale Potent Material Handling
• Cell Processing
• Aseptic Processing
• Research and Development
The retractable housings are intended solely for measurement tasks in conjunction with the specified METTLER TOLEDO electrodes/sensors, namely pH and redox (ORP) combined electrodes as well as dissolved oxygen (DO) or conductivity sensors.
لمبات تضيف تحديا جديدا إلى تقنيات تطهير و معالجة مياه الشرب بتكنولوجيا توزيع التدفق وSpektron إنها أنظمة
عالية الكفاءة, فهى تناسب محطات معالجة المياه القائمة بغض النظر عن حالة الأنابيب/المواسير المحلية EcoRay UV
أو جودة المياه حيث أن مفاعلات هذا النظام لديها القدرة على التعامل مع جودة المياه المنخفضة حتى 70% بنفاذية الأشعة فوق البنفسجية فى تطبيقات إمدادات المياه و الإستخدامات الصناعية و محطات المياه الضخمة بإنتاجية تتعدى 1000 متر مكعب/ الساعة للوحدة المجهزة بأنظمة إزالة خالية من المواد الكيميائية و تقنيات مراقبة و تحكم لكفاءة تشغيلية عالية بأقل تكلفة
http://rheoserve.com/index.html#portfolio
Precise control of low O2 set points with confidence.
CO detection for control interlocks and safety shutdown.
Predictive diagnostics
SIL 2 capable for SIS implementation of IEC 61508/61511 into the burner management system.
The reliable identification of low combustion oxygen in a red heater or boiler has always been critical to the effectiveness of the Burner Management System for proper control and safety.
Low emission burners and aggressive ring control points to achieve increased efficiency and emission reductions have driven the industry to tighter control measures. But tighter control measures also hold a greater potential for combustion damage. Reducing the risk of a combustion event has become a priority and has led to the implementation of Safety Instrumented Systems (SIS). This additional layer of safety is added to the Basic Process Control System.
www.envimart.vn - ĐT: 028 77727979 - sales@envimart.vn - Nền tảng cung cấp thiết bị, vật tư ngành nước và môi trường. Chuyên cung cấp vật tư cho dự án xử lý nước sạch, nước thải và môi trường. Envimart luôn đồng hành, tin cậy với đối tác nhà thầu, nhà tích hợp và người sử dụng.
www.envimart.vn - ĐT: 028 77727979 - sales@envimart.vn - Nền tảng cung cấp thiết bị, vật tư ngành nước và môi trường. Chuyên cung cấp vật tư cho dự án xử lý nước sạch, nước thải và môi trường. Envimart luôn đồng hành, tin cậy với đối tác nhà thầu, nhà tích hợp và người sử dụng.
WTW catalog process instrumentation in water industryENVIMART
Wtw catalog process instrumentation in water industry - WTW - Envimart JSC - www.envimart.vn - ĐT: 028 77727979 - sales@envimart.vn - Nền tảng cung cấp thiết bị, vật tư ngành nước và môi trường.
Precision water vapour permeability analysis of medical
& pharmaceutical packaging. Permeability testing is used in the design
and manufacture of blister packs, bottles,
pill containers, surgical dressings, needles
and syringe products.
www.envimart.vn - ĐT: 028 77727979 - sales@envimart.vn - Nền tảng cung cấp thiết bị, vật tư ngành nước và môi trường. Chuyên cung cấp vật tư cho dự án xử lý nước sạch, nước thải và môi trường. Envimart luôn đồng hành, tin cậy với đối tác nhà thầu, nhà tích hợp và người sử dụng.
Industry leaders in Desiccant Pouch and Cotton insertion systems. US built, unique technology to correctly cut. Widely proven reliable value. Speeds to 200+ bpm.
Unique Patented Hybrid Steam-Heat tunnels for shrink sleeve applications. Best & only one on the market, onboard steam, tiny footprint. Complements line of servo sleevers. North American built with SW technician. www.Aesus.com
Ang Chong Yi Navigating Singaporean Flavors: A Journey from Cultural Heritage...Ang Chong Yi
In the heart of Singapore, where tradition meets modernity, He embarks on a culinary adventure that transcends borders. His mission? Ang Chong Yi Exploring the Cultural Heritage and Identity in Singaporean Cuisine. To explore the rich tapestry of flavours that define Singaporean cuisine while embracing innovative plant-based approaches. Join us as we follow his footsteps through bustling markets, hidden hawker stalls, and vibrant street corners.
At Taste Of Middle East, we believe that food is not just about satisfying hunger, it's about experiencing different cultures and traditions. Our restaurant concept is based on selecting famous dishes from Iran, Turkey, Afghanistan, and other Arabic countries to give our customers an authentic taste of the Middle East
Roti Bank Hyderabad: A Beacon of Hope and NourishmentRoti Bank
One of the top cities of India, Hyderabad is the capital of Telangana and home to some of the biggest companies. But the other aspect of the city is a huge chunk of population that is even deprived of the food and shelter. There are many people in Hyderabad that are not having access to
3. Low power
long life x-ray
generator
Enhanced, high
sensitivity sensor
Low power, fully sealed
heat control system - Air
Conditioner Free!
Unique cooling solution
seals and protects the
system from outside air
exchange.
Controller
Anritsu's new x-ray technology exceeds the needs of today's demanding food
processing industry. In addition to contaminant detection the XR75 inspection system
can identify product shape defects and packaging integrity.
Superior image processing allows the Processor to see what they may have been
missing in previous x-ray system designs.
The highly engineered high sensitivity x-ray generator and sensor provide
outstanding sensitivity at lower energy levels. The result is superior performance,
extended life of cycles and reduced true cost of ownership.
The low output x-ray generator reduces heat generation, eliminating the need for
cooling system, resulting in a 30% reduction in power consumption.
The Anritsu XR75 x-ray inspection system can reduce the lifetime operating cost by
over 20%, as compared to other systems, making x-ray inspection more affordable to
purchase, own and operate.
Low generation of heat
Air-conditioner
free
High sensitivity
Long life
Low running
costs
Newly-developed sensor was
designed for both long life and
superior contaminant detection.
Low power design enables
longer component lifetime
while using less energy.
*1) Comparison with conventional models with air-conditioner. *2) It is the estimated value by Anritsu and may vary depending on the condition of machines.
3
Reducedtrue
costof
ownershipby
20%
ormore.*2
LongLife
X-Ray
Generator/
Sensor
Power
consumption
reduced by
30%*1
Air-
conditioner
free
Introducing Anritsu's Advanced
Long Life Technology
of X-ray inspection technology
4. Easy to operate
Simple step-by-step product setup
Product Registration Navigation simplifies parameter setting procedures with step-by-step illustrated instructions.
Simple maintenance
【Easy parts removal】No tools are required for removing/attaching the
conveyor belts and rollers including the front cover and x-ray leakage
prevention curtains.
【Easy-to-clean design】The system’s angled surfaces prevent water
from accumulating after system cleaning.
Simple information management
X-ray images and inspection logs can be saved to the USB memory for
HACCP compliance. All Anritsu systems can be connected, via Ethernet,
to QuiCCA. QuiCCA provides line status information, centralized
reporting and data storage. USB interface
(USB memory is optional)
Tool free belt removal
Sloped surfaces
for water run-off.
Overall quality management
and control system - QUICCA
4
5. Pasta
Asparagus
TubePlastic cupSyringe PrawnSliced meat Sausage
Cookie Chocolate Candy Instant beverage
XR75 provides accurate and repeatable detection of metals, wire, glass,
stone, calcified bones and other dense contaminants. ALL technology
was developed to provide high detection sensitivity and flexibility within
all products and packaging types.
Go Beyond Contaminant Detection
XR75 provides not only contaminant detection but also product
verfication simultaneously. Products can be inspected for missing
product, virtual weight, count, package check, void check, etc.
【Shape Detection】The shape, area and mass are analyzed from
x-ray images to find irregularities including breaks and chips. Missing
fillings can also be spotted.
【Missing Product Detection】Inspection for missing products are
available for those products in which the content is indicated by the
number, and the mass of each piece in a package varies per piece.
X-ray image of test pieces in 500g tenderloin. Accurate detection
of small Nylon and SUS spheres is now possible.
1 2
Cut sausageChipped biscuit
[Example of a package containing 12 cupcakes with 20 ±2 g each]
The weight of 11 pieces with 22 g each totals 242 g, which
satisfies weight requirement but the count is short.
Signal processing advancements allow detection of smaller
contaminants.
【Easy to adjust sensitivity】
Detection levels are visually shown on
the main screen to enhance usability.
Quick sensitivity adjustments are
possible (based on operator level).
HD imaging provides the best-in-industry detection.
P o i n t
5
XR75 delivers industry leading
detection for all products.
1 2
6. 6
Safety management
Anritsu believes customer safety is of utmost importance.
X-ray inspection system has been designed to fully satisfy the safe operation. However, to ensure even higher safety, use the
safety procedures outlined below.
Safety in design
Periodic measurement and recording of x-ray leakage data
Additional safety measures
Covers may need to be mounted on upstream and
downstream conveyors instead of the shield curtains,
depending on the shape, weight, and package of products.
Management of operator working hours
No disassembly or modification
NEVER modify or disassemble the main unit, covers, x-ray
leakage prevention curtains, safety covers, safety interlocks,
etc., otherwise the x-ray leak-proof design may no longer be
functional.
Anritsu safety mechanism
Emergency stop switch
Cuts power to x-ray and drive circuits, stops
the conveyor and x-ray radiation.
X-ray irradiation display
The lamp is lit during x-ray radiation.
Hand insertion sensor
Interrupting the sensor for a certain
period of time stops x-ray radiation.
Leakage prevention curtain
Prevents x-ray leakage. For
unpackaged or bulk products, the
standard lead impregnated curtains are
replaced with SUS covers - preventing
direct food contact with the curtains.
X-ray ON/OFF key
Turning the key to OFF stops x-ray radiation
completely.
X-ray shield cover open/close
sensor
Opening the cover stops x-ray radiation.
X-ray shield cover
Opened/Closed using x-ray Irradiation
ON/OFF Key.
Opening the cover stops x-ray radiation due
to the x-ray Shield Cover Open/Close Sensor.
1 2
3 4
Safety of inspected products
WHO concluded in 1980 that the “irradiation of any food commodity up to an overall average dose of 10 kGy presents no
toxicological hazard and introduces no special nutritional or microbiological problems.”
The maximum dose of x-ray irradiation to the products to be inspected by our x-ray inspection systems is 0.002 Gy, which is
much lower than the value described above. Even if a product stops inside, the x-ray dose is always kept to 0.1 Gy or less.
Note: Follow the local laws and regulations regarding the installation and use of the x-ray inspection systems.
7. External Dimensions
246
1440to1540
1620to1720
321Φ60Φ60
700to800
Lineheights
390
Effective
detection width
220
Passheight
550
Leg spacing
755
Leg spacing
240
Effective
detection width
550
Leg spacing
605
Leg spacing
120
Passheight
700to800
Lineheights
Φ33.5
Roller
Φ33.5
Roller
270
Beltwidth
KXS7534AWCLE
KXS7534AVCLE
KXS7522AWCLE
KXS7522AVCLE
730
(390)
500
800
500
800
(102)
315415
160
120
240
Dimensions in brackets are AVCLE type with waterproof on the entire surface. Units: mm
Detection area
420
Beltwidth
880
(390)
(102)
390490
230
220
390
Detection area
7
Specifications
For Packaged Products
Major specifications
Model KXS7522AWCLE KXS7522AVCLE KXS7534AWCLE KXS7534AVCLE
X-ray output Tube voltage 30 to 80 kV, tube current 0.4 to 3.3 mA, output 12 to 100 W
Safety X-ray leakage maximum 1.0 μSv/h or less, prevention of x-ray leakage by safety devices
Display 15-inch color TFT LCD
Operation method Touch panel (with touch buzzer)
Detection area 1, 2
Maximum width 240 mm, maximum height 120 mm Maximum width 390 mm, maximum height 220 mm
Belt width 270mm 420mm
Preset memory 200
Belt speed 3
/
Maximum product weight 4
10 to 60 m/min, maximum 5 kg 10 to 60 m/min, maximum 5 kg
60 to 90 m/min, maximum 2 kg ─
10 to 40 m/min, maximum 10 kg (optional) 10 to 40 m/min, maximum 10 kg (optional)
Power requirements 5
100 to 240 AC, single phase, 50/60 Hz, 700 VA or less (standard)
Mass 6
250kg 255kg 305kg 310kg
Environmental conditions 7, 8
Temperature: 0° to 35°C, Relative humidity: 30 to 85 %, non-condensing
Protection class Conveyor: IP66
Other parts: IP40
Entire surface conforms
to IP66
Conveyor: IP66
Other parts: IP40
Entire surface conforms
to IP66
Exterior Stainless steel (SUS304)
1 : The product size should fall below the detection area.
2 : The entrance and exit may require covers depending on the length of a product.
3 : Variable depending on Product No.
4 : Sum total of product weight on the conveyor.
5 : Allowable power fluctuation range is ± 10%.
6 : Mass without option
7 : For KXS7522AWCLE and KXS7522AVCLE, belt speed and maximum product weight are restricted at the temperature between
30°C and 35°C.
8 : The temperature between 0°C and 40°C when an optional air conditioner is installed. (AWCLE only)
8. 8
Major specifications
External Dimensions
KXS7534CWCLE
KXS7534CVCLE
KXS7522CWCLE
KXS7522CVCLE
For Lightweight Products
and Those in Small Bags
Specifications
1685to1815
320Φ60
700to800
Lineheights
390
Effective
detection width
30to50
Passheight
550
Leg spacing
755
Leg spacing
420
Beltwidth
Φ33.5
Roller
500
1340 to 1355
(390)
880(100)
390495
246
1500to1630
Φ60
240
Effective
detection width
550
Leg spacing
605
Leg spacing
30to50
Passheight
700to800
Lineheights
Φ33.5
Roller
270
Beltwidth
730
(390)
500
1340 to 1355
(100)
315415
10to15°
10to15°
220
240
Inclination angle of 10°
30
210
240
Inclination angle of 12.5°
40
200
240
Inclination angle of 15°
50
370
390
Inclination angle of 10°
30
360
390
Inclination angle of 12.5°
40
355
390
Inclination angle of 15°
50
Detection area Detection area
Dimensions in brackets are CVCLE type with waterproof on the entire surface. Units: mm
Model KXS7522CWCLE KXS7522CVCLE KXS7534CWCLE KXS7534CVCLE
X-ray output Tube voltage 25 to 60 kV, tube current 0.4 to 3.3 mA, output 10 to 100 W
Safety X-ray leakage maximum 1.0 μSv/h or less, prevention of x-ray leakage by safety devices
Display 15-inch color TFT LCD
Operation method Touch panel (with touch buzzer)
Detection area 1, 2
Maximum width 240 mm, maximum height 50 mm Maximum width 390 mm, maximum height 50 mm
Belt width 270mm 420mm
Preset memory 200
Belt speed 3
/
Maximum product weight 4 10 to 50 m/min, maximum 5 kg
Power requirements 5
100 to 240 AC, single phase, 50/60 Hz, 700 VA or less (standard)
Mass 6
280kg 285kg 340kg 345kg
Environmental conditions 7, 8
Temperature: 0° to 35°C, Relative humidity: 30 to 85 %, non-condensing
Protection class
Conveyor: IP66
Other parts: IP40
Entire surface conforms
to IP66
Conveyor: IP66
Other parts: IP40
Entire surface conforms
to IP66
Exterior Stainless steel (SUS304)
1 : The product size should fall below the detection area.
2 : The entrance and exit may require covers depending on the length of a product.
3 : Variable depending on Product No.
4 : Sum total of product weight on the conveyor.
5 : Allowable power fluctuation range is ± 10%.
6 : Mass without option
7 : For KXS7522CWCLE and KXS7522CVCLE, belt speed and maximum product weight are restricted at the temperature between
30°C and 35°C.
8 : The temperature between 0°C and 40°C when an optional air conditioner is installed. (CWCLE only)
Shield plate
Shield plate
X-ray leakage
prevention cover
9. 9
Major specifications
For Bulk Flow of Unpacked Fresh Food
Shield plate
Shield plate
X-ray leakage
prevention cover
This option is for those unpackaged products that require the inspection without the
leakage prevention curtain.
• Flow direction can be changed from left to right and vice versa.
• A separate modification is required for the change of flow direction after the
installation.
200
240
50
355
KXS7522AWCLE
KXS7522AVCLE
KXS7534AWCLE
KXS7534AVCLE
390
50
Detection area
Applicable models: KXS7522AWCLE, KXS7522AVCLE,
KXS7534AWCLE, KXS7534AVCLE
* Contact our sales representatives for details.
Note: Any one of the pass heights can be selected.
Model Detection area (Units:mm) Page
KXS7522AWCLE
KXS7522AVCLE
Effective detection width
Effective detection
7
KXS7522CWCLE
KXS7522CVCLE
Effective detection width
Effective detection
7
KXS7534AWCLE
KXS7534AVCLE
Effective detection width
Effective detection
8
KXS7534CWCLE
KXS7534CVCLE
Effective detection width
Effective detection
8
Products
X-ray radiationX-ray radiation
Products
Model Selection List