Lab Sales Corporation offers a wide range of laboratory chemicals, industrial chemicals, scientific instruments, and laboratory glassware. It has been operating since 1971 and is ISO 9001:2008 certified. The company procures products from reliable vendors and tests them to ensure they meet quality standards before supplying to customers. It aims to provide customized and quality products to customers in a timely manner.
This document outlines procedures and requirements for liquid penetrant examination. It discusses the scope of liquid penetrant examination, referencing documents, general procedures, equipment, requirements, examination process, evaluation, documentation, and definitions. Key steps include surface preparation, application of penetrant, removal of excess penetrant, application of developer, interpretation of results, and documentation. Contaminant control and certification are required for materials used to examine nickel alloys, austenitic stainless steels, and titanium.
Good Manufacturing PracticeFor LVP,SVP, ophthalmic veterinary medicine, bulk chemicals & invitro diagnostic
For Good business Practice
A control process gives reproducibility & product consistency with in known limits
Provides license to do business.
Validation may be defined as
“ Establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality attributes.”
Dry Heat
Moist Heat
Gas (Ethylene oxide)
Radiation (Gamma or Electron)
Filtration
Others - UV, Steam and formaldehyde, hydrogen peroxide
We, Naugra Export, are among the prominent manufacturers, supplier and exporters of Scientific and Laboratory Equipment. The offered product range offered by us is inclusive of Physics Lab Equipment, Biology Lab Equipment and Chemistry Lab Equipment. For the purpose of manufacturing this range, our professionals make use of latest tools and quality assured materials. For the ease of our valuable customers, we accept different modes of payment such as cash, credit card, demand draft and online. These scientific instruments offered by us find wide applications in schools and collages for carrying out physic, biology and chemistry laboratory. We are exporting our products all over the world.
This document discusses the validation of sterilization processes for sterile medicines. It defines sterility as a probability of less than 1 in 1 million of a container being contaminated. Sterilization methods discussed include moist heat, dry heat, ethylene oxide gas, radiation, and filtration. Validation of a sterilization process involves developing a protocol, calibrating instruments, developing sterilization cycles, and determining the necessary Fo value to achieve the required sterility assurance level based on the bioburden and most resistant organisms. Moist heat sterilization at 121°C for 15 minutes is provided as an example, which would achieve an Fo value of 15.
MDC Machine Design has recently worked on a variety of projects including:
1. Developing an autosampler for highly viscous compounds and a control cabinet for a pharmaceutical application.
2. Designing animal workstations for behavioral studies and an attitude sensor.
3. Fabricating machines for pharmaceutical processing, studying impacts on multi-dose vials, and containing vacuum pump noise and heat in a laboratory.
This document outlines procedures and requirements for liquid penetrant examination. It discusses the scope of liquid penetrant examination, referencing documents, general procedures, equipment, requirements, examination process, evaluation, documentation, and definitions. Key steps include surface preparation, application of penetrant, removal of excess penetrant, application of developer, interpretation of results, and documentation. Contaminant control and certification are required for materials used to examine nickel alloys, austenitic stainless steels, and titanium.
Good Manufacturing PracticeFor LVP,SVP, ophthalmic veterinary medicine, bulk chemicals & invitro diagnostic
For Good business Practice
A control process gives reproducibility & product consistency with in known limits
Provides license to do business.
Validation may be defined as
“ Establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality attributes.”
Dry Heat
Moist Heat
Gas (Ethylene oxide)
Radiation (Gamma or Electron)
Filtration
Others - UV, Steam and formaldehyde, hydrogen peroxide
We, Naugra Export, are among the prominent manufacturers, supplier and exporters of Scientific and Laboratory Equipment. The offered product range offered by us is inclusive of Physics Lab Equipment, Biology Lab Equipment and Chemistry Lab Equipment. For the purpose of manufacturing this range, our professionals make use of latest tools and quality assured materials. For the ease of our valuable customers, we accept different modes of payment such as cash, credit card, demand draft and online. These scientific instruments offered by us find wide applications in schools and collages for carrying out physic, biology and chemistry laboratory. We are exporting our products all over the world.
This document discusses the validation of sterilization processes for sterile medicines. It defines sterility as a probability of less than 1 in 1 million of a container being contaminated. Sterilization methods discussed include moist heat, dry heat, ethylene oxide gas, radiation, and filtration. Validation of a sterilization process involves developing a protocol, calibrating instruments, developing sterilization cycles, and determining the necessary Fo value to achieve the required sterility assurance level based on the bioburden and most resistant organisms. Moist heat sterilization at 121°C for 15 minutes is provided as an example, which would achieve an Fo value of 15.
MDC Machine Design has recently worked on a variety of projects including:
1. Developing an autosampler for highly viscous compounds and a control cabinet for a pharmaceutical application.
2. Designing animal workstations for behavioral studies and an attitude sensor.
3. Fabricating machines for pharmaceutical processing, studying impacts on multi-dose vials, and containing vacuum pump noise and heat in a laboratory.
One slider for qualification and validation of depyrogenation and sterilizati...Palash Das
This document provides a qualification and validation matrix for a sterilization tunnel. It outlines various tests to verify performance, including air velocity, filter leakage, differential pressure, airflow visualization, conveyor speed, non-viable particle count, heat distribution, and endotoxin challenge studies. For each test, it describes the purpose, acceptance criteria, test frequency, and methodology. The goal is to ensure the sterilization tunnel achieves proper depyrogenation and sterilization through regular performance testing.
The JLab Instruments Leak Test Apparatus is used to test the quality of packaging seals for food, drugs, and other products contained in strips, blisters, and sachets. It generates a vacuum inside a desiccator housing to test if the packaging retains its shape or if dye penetrates through any holes in the seals when immersed in a solution after the vacuum is released. The instrument features a microcontroller, LED display, soft-touch keys, and integrated vacuum pump for creating vacuum within 30 seconds to hold for a preset time up to 9999 seconds.
The document describes the operation and validation of an industrial double door autoclave. It provides details on the various sterilization cycles used - vacuum leak test, Bowie-Dick test, steam in process test, gravity cycle, and high pressure high vacuum cycle. The procedures, parameters, and results of running these cycles to validate the autoclave are presented. The conclusion is that the autoclave satisfies all United States Pharmacopeia parameters and can be used for sterilization.
Leak Testing: Different Types Of Leak Testing Methods | Helium Leak Testing Kryovess Pvt. Ltd.
Leak testing method is a very known and important method using for leak detection in the industries. Leak test and leak detection using air decay, helium or water submerse methods. The choice of the detection method depends on which method is most appropriate for the system at hand. Leak testing methods each have their own sensitivity, expressed as the lowest leak rate the method can detect. Highly sensitive methods are required to test highly leak prone systems such as vacuum systems.
This document provides information on air filter testing equipment from FEC. It describes testing systems that can test various types of air filters according to standards like EN 779 and ASHRAE 52.2. The systems can test parameters like flow rate, differential pressure, dust holding capacity, and efficiency. They include components like test ducts, centrifugal blowers, aerosol generators, and particle counters. FEC offers customizable filter testing solutions at various throughput capacities.
The distinguished manufacturers and suppliers of a perfect range of precision engineered Testing equipments. Extensively appreciated for its superior quality, these machines find wide industrial applications such as Ultrasound Machine, Bod IncubatorFully Automatic Chemistry Analyzer, Semi Automatic Chemistry Analyzer, Latex Examination Gloves, Disposables..
HPTLC is an enhanced form of thin layer chromatography that provides high accuracy and precision. It consists of a sample applicator, developing chamber, derivatization device, immersion device, plate heater, and scanning densitometer. Samples are applied in spots or bands on a plate and developed in a chamber to separate components based on their affinities to the stationary phase. Components can then be detected visually or through a densitometer, and unknowns can be identified by comparing to standards. HPTLC is useful for herbal analysis, purity determination, and identification of compounds.
Test Master has opened a world-class filter testing lab in Delhi, India that can test a wide range of filters and filtration media according to national and international standards. The lab has experienced engineers and equipment to test items like air, oil, fuel, and hydraulic filters. Testing includes measuring filter performance, materials integrity, efficiency, and other key filter properties. The lab aims to provide a one-stop solution for filter and media testing needs according to standards like ISO, SAE, and others. NABL accreditation of the lab is in process.
This document discusses validation of steam sterilization processes. It provides information on key terms used in microbial death kinetics like D values, Z values, and F values. It presents formulas used to calculate these values. The document also discusses autoclave calibration methods, including using boiling water and multipoint calibration. An example standard operating procedure for autoclave calibration is given. Common problems with steam sterilization validation are listed.
The document discusses the validation of various sterilization methods and water supply systems used in pharmaceutical manufacturing. It provides details on:
1. The key properties of sterile products and various sterilization methods like heat, gas, radiation.
2. The validation process for steam, dry heat and ethylene oxide sterilization including qualification of equipment and instruments, heat distribution studies, biological indicators, and establishing a monitoring program.
3. Types of water systems used, water treatment techniques, equipment components, design considerations for storage and distribution, and the concept of validation involving engineering design, operating procedures, maintenance and testing under all conditions.
This document discusses high performance thin layer chromatography (HPTLC). It describes the principles of HPTLC, which uses adsorption chromatography to separate components based on their affinity for the stationary and mobile phases. The key features, steps, and instrumentation of HPTLC are outlined. Various applications of HPTLC in fields like herbal analysis, pharmaceutical science, and forensics are mentioned. The document also discusses qualification processes like installation qualification and operation qualification that are important for cGMP regulated environments using HPTLC.
Steam sterilization uses high-pressure steam to kill microorganisms. It is the most effective sterilization method when heat and moisture do not damage products. An autoclave uses steam to heat items inside a pressurized chamber, reaching temperatures over 121°C. Validation of a sterilization process involves qualification of the autoclave design, installation, operation, and performance through studies measuring temperature distribution, heat penetration, and using biological indicators to confirm a sterilization log reduction factor is achieved.
Joe McCarthy, Dell Tech Laboratories Lab Services Manager will introduce you to Corrositex®/OECD 435 and demonstrate:
• How easily you can perform Corrositex®
• What you need to perform Corrositex®
• Time & cost advantages of Corrositex®
• Regulatory acceptance of Corrositex®
For full webinar video see: https://www.youtube.com/watch?v=sDPreBmZnPM&t=94s
Visual inspection of parenteral products is conducted to detect defective units and ensure compliance with regulatory requirements that injectable products be free of visible particles. All filled containers undergo 100% visual inspection against black and white backgrounds under controlled lighting. Inspections are usually manual but can also be automated. Post-inspection sampling is required and failures can result in batch rejection. Any particles detected must be characterized to identify the source and ensure appropriate corrective actions. Recalls are sometimes necessary when particles are found, posing a risk to patient safety. Thorough training and documentation are needed to support consistent visual inspection.
6 CLASSES OF CHEMICAL INDICATORS FOR STEAM STERILIZATIONaccessamg
Chemical indicators for autoclaves and steam sterilizers play a critical role in sterility assurance programs. There are many types of chemical indicators, such as bowie dick test packs and chemical indicator strips.
All chemical indicators are designed to respond to physical conditions inside the sterilizing chamber. This validates that an autoclave or steam sterilizer is working properly. It also verifies that it met the conditions for sterilization to occur.
Steam sterilization monitoring involves ensuring sterilized items are free from microorganisms. The document discusses several key aspects of steam sterilization monitoring including: (1) sterility assurance levels and D-values which define sterilization effectiveness, (2) common sterilization methods like steam, gamma radiation and hydrogen peroxide, (3) methods for monitoring sterilization like mechanical, chemical and biological indicators, and (4) levels of assurance including equipment, exposure, pack and load control through proper use of indicators and record keeping. Managing a positive biological indicator requires recalling implantable items, retesting the sterilizer, and putting it back in service only after three consecutive negative retests.
Validation is the process of checking of the process, equipment and method whereas qualification is solely done for equipment and qualification of instrument helps in quality of pharmaceutical product.
This document discusses visual inspection of drug products for defects and container integrity. It summarizes regulations around ensuring container closure systems provide adequate protection and rejecting drug products that fail to meet standards. The document also discusses recalls related to visible particulates and FDA observations around visual inspection issues. It provides an overview of differences between human and automated inspections. A survey found manual inspection is most common and discusses typical inspection conditions and rejection rates. Key aspects of USP <790> on visible particulates in injections are also summarized, including inspection illumination, times, and acceptance criteria. The document concludes that while inspection cannot ensure products are 100% defect free, practical limits and patient risk guide the process.
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.
Texcare Industries manufactures and supplies a wide range of textile testing equipment and accessories. This includes fiber and yarn testing equipment, garment testing equipment, fabric testing equipment, textile testing consumables, optical tools and microscopes, measuring instruments, lab dyeing machines, and special lights. The company was established in 2009 and exports products to Southeast Asia and the Indian subcontinent.
Exporters of Reflex Klyston Microwave Test Bench, Voltage DoublerTripler Circuit, Kjeldhal Digestion Distillation Unit, Pathological Medical Research Microscope, Kjeldhal Digestion and Distillation Unit, Soxhlet Extraction Unit with Energy Regulator.
One slider for qualification and validation of depyrogenation and sterilizati...Palash Das
This document provides a qualification and validation matrix for a sterilization tunnel. It outlines various tests to verify performance, including air velocity, filter leakage, differential pressure, airflow visualization, conveyor speed, non-viable particle count, heat distribution, and endotoxin challenge studies. For each test, it describes the purpose, acceptance criteria, test frequency, and methodology. The goal is to ensure the sterilization tunnel achieves proper depyrogenation and sterilization through regular performance testing.
The JLab Instruments Leak Test Apparatus is used to test the quality of packaging seals for food, drugs, and other products contained in strips, blisters, and sachets. It generates a vacuum inside a desiccator housing to test if the packaging retains its shape or if dye penetrates through any holes in the seals when immersed in a solution after the vacuum is released. The instrument features a microcontroller, LED display, soft-touch keys, and integrated vacuum pump for creating vacuum within 30 seconds to hold for a preset time up to 9999 seconds.
The document describes the operation and validation of an industrial double door autoclave. It provides details on the various sterilization cycles used - vacuum leak test, Bowie-Dick test, steam in process test, gravity cycle, and high pressure high vacuum cycle. The procedures, parameters, and results of running these cycles to validate the autoclave are presented. The conclusion is that the autoclave satisfies all United States Pharmacopeia parameters and can be used for sterilization.
Leak Testing: Different Types Of Leak Testing Methods | Helium Leak Testing Kryovess Pvt. Ltd.
Leak testing method is a very known and important method using for leak detection in the industries. Leak test and leak detection using air decay, helium or water submerse methods. The choice of the detection method depends on which method is most appropriate for the system at hand. Leak testing methods each have their own sensitivity, expressed as the lowest leak rate the method can detect. Highly sensitive methods are required to test highly leak prone systems such as vacuum systems.
This document provides information on air filter testing equipment from FEC. It describes testing systems that can test various types of air filters according to standards like EN 779 and ASHRAE 52.2. The systems can test parameters like flow rate, differential pressure, dust holding capacity, and efficiency. They include components like test ducts, centrifugal blowers, aerosol generators, and particle counters. FEC offers customizable filter testing solutions at various throughput capacities.
The distinguished manufacturers and suppliers of a perfect range of precision engineered Testing equipments. Extensively appreciated for its superior quality, these machines find wide industrial applications such as Ultrasound Machine, Bod IncubatorFully Automatic Chemistry Analyzer, Semi Automatic Chemistry Analyzer, Latex Examination Gloves, Disposables..
HPTLC is an enhanced form of thin layer chromatography that provides high accuracy and precision. It consists of a sample applicator, developing chamber, derivatization device, immersion device, plate heater, and scanning densitometer. Samples are applied in spots or bands on a plate and developed in a chamber to separate components based on their affinities to the stationary phase. Components can then be detected visually or through a densitometer, and unknowns can be identified by comparing to standards. HPTLC is useful for herbal analysis, purity determination, and identification of compounds.
Test Master has opened a world-class filter testing lab in Delhi, India that can test a wide range of filters and filtration media according to national and international standards. The lab has experienced engineers and equipment to test items like air, oil, fuel, and hydraulic filters. Testing includes measuring filter performance, materials integrity, efficiency, and other key filter properties. The lab aims to provide a one-stop solution for filter and media testing needs according to standards like ISO, SAE, and others. NABL accreditation of the lab is in process.
This document discusses validation of steam sterilization processes. It provides information on key terms used in microbial death kinetics like D values, Z values, and F values. It presents formulas used to calculate these values. The document also discusses autoclave calibration methods, including using boiling water and multipoint calibration. An example standard operating procedure for autoclave calibration is given. Common problems with steam sterilization validation are listed.
The document discusses the validation of various sterilization methods and water supply systems used in pharmaceutical manufacturing. It provides details on:
1. The key properties of sterile products and various sterilization methods like heat, gas, radiation.
2. The validation process for steam, dry heat and ethylene oxide sterilization including qualification of equipment and instruments, heat distribution studies, biological indicators, and establishing a monitoring program.
3. Types of water systems used, water treatment techniques, equipment components, design considerations for storage and distribution, and the concept of validation involving engineering design, operating procedures, maintenance and testing under all conditions.
This document discusses high performance thin layer chromatography (HPTLC). It describes the principles of HPTLC, which uses adsorption chromatography to separate components based on their affinity for the stationary and mobile phases. The key features, steps, and instrumentation of HPTLC are outlined. Various applications of HPTLC in fields like herbal analysis, pharmaceutical science, and forensics are mentioned. The document also discusses qualification processes like installation qualification and operation qualification that are important for cGMP regulated environments using HPTLC.
Steam sterilization uses high-pressure steam to kill microorganisms. It is the most effective sterilization method when heat and moisture do not damage products. An autoclave uses steam to heat items inside a pressurized chamber, reaching temperatures over 121°C. Validation of a sterilization process involves qualification of the autoclave design, installation, operation, and performance through studies measuring temperature distribution, heat penetration, and using biological indicators to confirm a sterilization log reduction factor is achieved.
Joe McCarthy, Dell Tech Laboratories Lab Services Manager will introduce you to Corrositex®/OECD 435 and demonstrate:
• How easily you can perform Corrositex®
• What you need to perform Corrositex®
• Time & cost advantages of Corrositex®
• Regulatory acceptance of Corrositex®
For full webinar video see: https://www.youtube.com/watch?v=sDPreBmZnPM&t=94s
Visual inspection of parenteral products is conducted to detect defective units and ensure compliance with regulatory requirements that injectable products be free of visible particles. All filled containers undergo 100% visual inspection against black and white backgrounds under controlled lighting. Inspections are usually manual but can also be automated. Post-inspection sampling is required and failures can result in batch rejection. Any particles detected must be characterized to identify the source and ensure appropriate corrective actions. Recalls are sometimes necessary when particles are found, posing a risk to patient safety. Thorough training and documentation are needed to support consistent visual inspection.
6 CLASSES OF CHEMICAL INDICATORS FOR STEAM STERILIZATIONaccessamg
Chemical indicators for autoclaves and steam sterilizers play a critical role in sterility assurance programs. There are many types of chemical indicators, such as bowie dick test packs and chemical indicator strips.
All chemical indicators are designed to respond to physical conditions inside the sterilizing chamber. This validates that an autoclave or steam sterilizer is working properly. It also verifies that it met the conditions for sterilization to occur.
Steam sterilization monitoring involves ensuring sterilized items are free from microorganisms. The document discusses several key aspects of steam sterilization monitoring including: (1) sterility assurance levels and D-values which define sterilization effectiveness, (2) common sterilization methods like steam, gamma radiation and hydrogen peroxide, (3) methods for monitoring sterilization like mechanical, chemical and biological indicators, and (4) levels of assurance including equipment, exposure, pack and load control through proper use of indicators and record keeping. Managing a positive biological indicator requires recalling implantable items, retesting the sterilizer, and putting it back in service only after three consecutive negative retests.
Validation is the process of checking of the process, equipment and method whereas qualification is solely done for equipment and qualification of instrument helps in quality of pharmaceutical product.
This document discusses visual inspection of drug products for defects and container integrity. It summarizes regulations around ensuring container closure systems provide adequate protection and rejecting drug products that fail to meet standards. The document also discusses recalls related to visible particulates and FDA observations around visual inspection issues. It provides an overview of differences between human and automated inspections. A survey found manual inspection is most common and discusses typical inspection conditions and rejection rates. Key aspects of USP <790> on visible particulates in injections are also summarized, including inspection illumination, times, and acceptance criteria. The document concludes that while inspection cannot ensure products are 100% defect free, practical limits and patient risk guide the process.
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.
Texcare Industries manufactures and supplies a wide range of textile testing equipment and accessories. This includes fiber and yarn testing equipment, garment testing equipment, fabric testing equipment, textile testing consumables, optical tools and microscopes, measuring instruments, lab dyeing machines, and special lights. The company was established in 2009 and exports products to Southeast Asia and the Indian subcontinent.
Exporters of Reflex Klyston Microwave Test Bench, Voltage DoublerTripler Circuit, Kjeldhal Digestion Distillation Unit, Pathological Medical Research Microscope, Kjeldhal Digestion and Distillation Unit, Soxhlet Extraction Unit with Energy Regulator.
Manufacturers and exporters of Deep Freezer, Water Bath Shaker, Laminar Flow Cabinet, Bench Top Laminar Flow, Bio Safety Lab Cabinet, Bacteriological Laboratory Incubator, Bio Safety Cabinet, Incubator Shakers, Vertical Autoclave
We are counted as a prominent importer, distributor, exporter and stockist of a wide range of Agricultural and Electrical Measuring Instrument. These products are used in pharmaceutical, plant & machinery, agriculture and electronic industries.
We, Veekay Industries, established our presence in 1959 as a manufacturer, exporter and supplier of a comprehensive assortment of testing machines such as Laboratory Testing Equipment, Strength of Material Lab Equipments and Computerized Universal Testing Machine.
We are manufacturer & exporter of a qualitative range of Engineering LAB Equipment & Special Purpose Machine. We emphases on the quality assurance & production techniques to provide products with increased reliability.
Associate Agencies, are engaged in manufacturing, supplying, trading and exporting a wide range of Inspection, Testing and Measuring Instruments. These products are known for their durability, reliability and excellent performance.
Exports enjoys an enormous reputation in the market as a seasoned Exporters of Scientific and Lab Instruments such that Hand Tools, Adapter 3 Way Glass, Vacuum Adapter Glass, Allhin Condenser Glass, Student Microscope, Medical Microscope, Stereo Microscope, Binocular Microscope..
We are a proficient company known for manufacturing and supplying sophisticated range of Industrial Weighing Scales, Industrial Weighing Systems, Colour Light Appearance Measurement and many more.
The renowned distributor and supplier For qualitative Electronic Laboratory Balance & Laboratory Instruments. These machines are widely appreciated by the clients for their reliability, accuracy Ultra Micro Balance, MYA/2Y Micro Balances, MYA/2Y 21/P Microbalance For Calibration Of Pipettes, MYA/2Y/F Microbalances For Filter Weighing, Laboratory Analytical Balances, Laboratory Analytical Balances, Laboratory Balance
With our industry experience from 2003, we, Esel International known for Manufacturer and Exporter, we have been able to offer precision engineered range of scientific physics lab wares, scientific chemistry lab wares and scientific biology lab wares, such as Magnetic Instruments, Rheostats, Physics Instruments, Light and Optics, Laboratory Meters, Stand and Clamps, Laboratory Oven, Anatomical Models, Binocular Microscope, Breadboard Kits, Educational Electronic Instruments.
We are one of the leading manufacturers, exporters and suppliers of Metal Testing Machines that have a wide demand in the market. In our organization, we have a team of experts who manufacture these machines with accurate dimensions that gives superior and reliable performance without any problem.
Labline Stock Centre is a manufacturer and supplier of laboratory equipment and scientific instruments established in 1986. They offer a wide range of products such as microscopes, meters, ovens, incubators, and autoclaves used in labs and research centers. The company prides itself on using high-quality materials and customizing products to meet specified client requirements.
This document provides information about Innovative Research Equipments, a manufacturer and exporter of laboratory equipment. The company produces a range of equipment including heat transfer, fluid mechanics, chemical reaction, and process control devices. It has an ISO certified facility with advanced machinery used to test products before export. Innovative Research also offers customized equipment design and fabrication to meet clients' specific needs.
We are recognized as one of the prominent Trader, Exporter, and Supplier of wide array of quality control and research & development equipment. We offer these products at pocket friendly rates to our clients.
Founded in the year, 1992, ‘Quality Instruments and Equipments’, is engaged in manufacturing, supplying and exporting a wide gamut of Pharmaceutical and Laboratory Equipments. We offer a quality range of Cashew Equipment, Labratory Equipment and Laboratory Oven to our clients. These products are manufactured using superior quality raw material and sophisticated technology. We procure the complete raw material from certified market vendors after conducting thorough market surveys. These products are in huge demand due to their unique features like durability, great performance and high efficiency. We export our products to Dubai and Africa.
Quality Instruments & Equipments is a leading manufacturer and exporter of laboratory, pharmaceutical, and industrial instruments established in 1992. They offer a wide range of products including cashew equipment, laboratory equipment, laboratory ovens, industrial equipment, and more. Their high-quality products are in demand for their durability, performance, and efficiency. Under the leadership of Mr. Gaurav Mestry, the company has established itself as a top supplier in the industry.
SGM Lab Solutions an initiative of SIGMA TEST & RESEARCH CENTRE was established in 2008 by technocrat educationists who have over 30 years of experience in the area of education, administration, manufacturing & marketing.
We are leading manufacturer & supplier of drawing, survey, mathematical, hydrological, maps, civil, soil testing instrument, structural and fluid mechanics lab.
Exporters of Pensky Martin Flash Point Apparatus, Redwood Viscometer, Kinematic Viscometer Bath, Saybolt Viscometer, Physical Balance, Chemical Balance, Analytical Balance, Personal Weighing Machine.
HCL Notes und Domino Lizenzkostenreduzierung in der Welt von DLAUpanagenda
Webinar Recording: https://www.panagenda.com/webinars/hcl-notes-und-domino-lizenzkostenreduzierung-in-der-welt-von-dlau/
DLAU und die Lizenzen nach dem CCB- und CCX-Modell sind für viele in der HCL-Community seit letztem Jahr ein heißes Thema. Als Notes- oder Domino-Kunde haben Sie vielleicht mit unerwartet hohen Benutzerzahlen und Lizenzgebühren zu kämpfen. Sie fragen sich vielleicht, wie diese neue Art der Lizenzierung funktioniert und welchen Nutzen sie Ihnen bringt. Vor allem wollen Sie sicherlich Ihr Budget einhalten und Kosten sparen, wo immer möglich. Das verstehen wir und wir möchten Ihnen dabei helfen!
Wir erklären Ihnen, wie Sie häufige Konfigurationsprobleme lösen können, die dazu führen können, dass mehr Benutzer gezählt werden als nötig, und wie Sie überflüssige oder ungenutzte Konten identifizieren und entfernen können, um Geld zu sparen. Es gibt auch einige Ansätze, die zu unnötigen Ausgaben führen können, z. B. wenn ein Personendokument anstelle eines Mail-Ins für geteilte Mailboxen verwendet wird. Wir zeigen Ihnen solche Fälle und deren Lösungen. Und natürlich erklären wir Ihnen das neue Lizenzmodell.
Nehmen Sie an diesem Webinar teil, bei dem HCL-Ambassador Marc Thomas und Gastredner Franz Walder Ihnen diese neue Welt näherbringen. Es vermittelt Ihnen die Tools und das Know-how, um den Überblick zu bewahren. Sie werden in der Lage sein, Ihre Kosten durch eine optimierte Domino-Konfiguration zu reduzieren und auch in Zukunft gering zu halten.
Diese Themen werden behandelt
- Reduzierung der Lizenzkosten durch Auffinden und Beheben von Fehlkonfigurationen und überflüssigen Konten
- Wie funktionieren CCB- und CCX-Lizenzen wirklich?
- Verstehen des DLAU-Tools und wie man es am besten nutzt
- Tipps für häufige Problembereiche, wie z. B. Team-Postfächer, Funktions-/Testbenutzer usw.
- Praxisbeispiele und Best Practices zum sofortigen Umsetzen
Goodbye Windows 11: Make Way for Nitrux Linux 3.5.0!SOFTTECHHUB
As the digital landscape continually evolves, operating systems play a critical role in shaping user experiences and productivity. The launch of Nitrux Linux 3.5.0 marks a significant milestone, offering a robust alternative to traditional systems such as Windows 11. This article delves into the essence of Nitrux Linux 3.5.0, exploring its unique features, advantages, and how it stands as a compelling choice for both casual users and tech enthusiasts.
Let's Integrate MuleSoft RPA, COMPOSER, APM with AWS IDP along with Slackshyamraj55
Discover the seamless integration of RPA (Robotic Process Automation), COMPOSER, and APM with AWS IDP enhanced with Slack notifications. Explore how these technologies converge to streamline workflows, optimize performance, and ensure secure access, all while leveraging the power of AWS IDP and real-time communication via Slack notifications.
Building Production Ready Search Pipelines with Spark and MilvusZilliz
Spark is the widely used ETL tool for processing, indexing and ingesting data to serving stack for search. Milvus is the production-ready open-source vector database. In this talk we will show how to use Spark to process unstructured data to extract vector representations, and push the vectors to Milvus vector database for search serving.
UiPath Test Automation using UiPath Test Suite series, part 6DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 6. In this session, we will cover Test Automation with generative AI and Open AI.
UiPath Test Automation with generative AI and Open AI webinar offers an in-depth exploration of leveraging cutting-edge technologies for test automation within the UiPath platform. Attendees will delve into the integration of generative AI, a test automation solution, with Open AI advanced natural language processing capabilities.
Throughout the session, participants will discover how this synergy empowers testers to automate repetitive tasks, enhance testing accuracy, and expedite the software testing life cycle. Topics covered include the seamless integration process, practical use cases, and the benefits of harnessing AI-driven automation for UiPath testing initiatives. By attending this webinar, testers, and automation professionals can gain valuable insights into harnessing the power of AI to optimize their test automation workflows within the UiPath ecosystem, ultimately driving efficiency and quality in software development processes.
What will you get from this session?
1. Insights into integrating generative AI.
2. Understanding how this integration enhances test automation within the UiPath platform
3. Practical demonstrations
4. Exploration of real-world use cases illustrating the benefits of AI-driven test automation for UiPath
Topics covered:
What is generative AI
Test Automation with generative AI and Open AI.
UiPath integration with generative AI
Speaker:
Deepak Rai, Automation Practice Lead, Boundaryless Group and UiPath MVP
AI 101: An Introduction to the Basics and Impact of Artificial IntelligenceIndexBug
Imagine a world where machines not only perform tasks but also learn, adapt, and make decisions. This is the promise of Artificial Intelligence (AI), a technology that's not just enhancing our lives but revolutionizing entire industries.
Driving Business Innovation: Latest Generative AI Advancements & Success StorySafe Software
Are you ready to revolutionize how you handle data? Join us for a webinar where we’ll bring you up to speed with the latest advancements in Generative AI technology and discover how leveraging FME with tools from giants like Google Gemini, Amazon, and Microsoft OpenAI can supercharge your workflow efficiency.
During the hour, we’ll take you through:
Guest Speaker Segment with Hannah Barrington: Dive into the world of dynamic real estate marketing with Hannah, the Marketing Manager at Workspace Group. Hear firsthand how their team generates engaging descriptions for thousands of office units by integrating diverse data sources—from PDF floorplans to web pages—using FME transformers, like OpenAIVisionConnector and AnthropicVisionConnector. This use case will show you how GenAI can streamline content creation for marketing across the board.
Ollama Use Case: Learn how Scenario Specialist Dmitri Bagh has utilized Ollama within FME to input data, create custom models, and enhance security protocols. This segment will include demos to illustrate the full capabilities of FME in AI-driven processes.
Custom AI Models: Discover how to leverage FME to build personalized AI models using your data. Whether it’s populating a model with local data for added security or integrating public AI tools, find out how FME facilitates a versatile and secure approach to AI.
We’ll wrap up with a live Q&A session where you can engage with our experts on your specific use cases, and learn more about optimizing your data workflows with AI.
This webinar is ideal for professionals seeking to harness the power of AI within their data management systems while ensuring high levels of customization and security. Whether you're a novice or an expert, gain actionable insights and strategies to elevate your data processes. Join us to see how FME and AI can revolutionize how you work with data!
Maruthi Prithivirajan, Head of ASEAN & IN Solution Architecture, Neo4j
Get an inside look at the latest Neo4j innovations that enable relationship-driven intelligence at scale. Learn more about the newest cloud integrations and product enhancements that make Neo4j an essential choice for developers building apps with interconnected data and generative AI.
How to Get CNIC Information System with Paksim Ga.pptxdanishmna97
Pakdata Cf is a groundbreaking system designed to streamline and facilitate access to CNIC information. This innovative platform leverages advanced technology to provide users with efficient and secure access to their CNIC details.
UiPath Test Automation using UiPath Test Suite series, part 5DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 5. In this session, we will cover CI/CD with devops.
Topics covered:
CI/CD with in UiPath
End-to-end overview of CI/CD pipeline with Azure devops
Speaker:
Lyndsey Byblow, Test Suite Sales Engineer @ UiPath, Inc.
In the rapidly evolving landscape of technologies, XML continues to play a vital role in structuring, storing, and transporting data across diverse systems. The recent advancements in artificial intelligence (AI) present new methodologies for enhancing XML development workflows, introducing efficiency, automation, and intelligent capabilities. This presentation will outline the scope and perspective of utilizing AI in XML development. The potential benefits and the possible pitfalls will be highlighted, providing a balanced view of the subject.
We will explore the capabilities of AI in understanding XML markup languages and autonomously creating structured XML content. Additionally, we will examine the capacity of AI to enrich plain text with appropriate XML markup. Practical examples and methodological guidelines will be provided to elucidate how AI can be effectively prompted to interpret and generate accurate XML markup.
Further emphasis will be placed on the role of AI in developing XSLT, or schemas such as XSD and Schematron. We will address the techniques and strategies adopted to create prompts for generating code, explaining code, or refactoring the code, and the results achieved.
The discussion will extend to how AI can be used to transform XML content. In particular, the focus will be on the use of AI XPath extension functions in XSLT, Schematron, Schematron Quick Fixes, or for XML content refactoring.
The presentation aims to deliver a comprehensive overview of AI usage in XML development, providing attendees with the necessary knowledge to make informed decisions. Whether you’re at the early stages of adopting AI or considering integrating it in advanced XML development, this presentation will cover all levels of expertise.
By highlighting the potential advantages and challenges of integrating AI with XML development tools and languages, the presentation seeks to inspire thoughtful conversation around the future of XML development. We’ll not only delve into the technical aspects of AI-powered XML development but also discuss practical implications and possible future directions.
2. A Member of
A b o u t U s
Established in the year 1971, we, “Lab Sales Corporation”, are ISO 9001:2008 certified
organization engaged in trading and exporting a premium range of Industrial Chemicals,
Scientific Instruments and Glass Apparatus. We procure these products from the reliable
vendors of the market, who make them using superior quality raw material in accordance to international
quality standards. Further, we have a team of quality analyzers who stringently test these products on
various parameters to ensure flawless range of products. We lay all possible efforts in order to provide
utmost satisfaction to the clients. In addition to this, we provide customization as per the exact
specifications laid down by the customers.
Our Product range includes Electrochemical Instrument, Laboratory Scientific
Instruments, Laboratory Equipments, Laboratory Autoclave Instrument, Laboratory
Refractometer Instrument, Laboratory Glassware Instrument, Standard Instrument,
P.H. Meter Instrument, Laboratory Instruments, Laboratory Autoclave, Measuring
Instruments, Laboratory Incubator Instrument, Hand Refractometers Instrument, etc.
We have developed a sophisticated state-of-the-art infrastructure which is spread over a wide area of
200 square feet. Equipped with latest machinery, tools and equipment, our infrastructure caters to the
emerging demands of the customers. We have segregated our infrastructure into various units in order
to fulfill the bulk requirements of the clients in best possible way. Further, we have highly dedicated and
diligent tram of professionals which help us in providing quality-approved range of products to the
customers. They make sure that every products should be in accordance to international quality
standards. In addition to this, our team of packaging ensure the qualitative packing of products and
delivering those products within the stipulated time frame.
7. A Member of
F a c t s h e e t
Year of Establishment : 1971
Nature of Business : Importer, Distributor, Exporter, Trader
Total Number of Employees : Upto 10 People
Primary Competitive Advantage : Experienced R & D Department
8. A Member of
CONTACT US
Lab Sales Corporation
Contact Person: Mr. Bharat Bist
1053, Phatak Muftiwalan, Tiraha Behram Khan, Darya Ganj
New Delhi - 110 002, Delhi, India
08376806479
www.labsalescorporation.com