http://www.thermoscientific.com/en/product/virtuoso-vial-identification-system.html
First of its kind vial identification system, that removes manual vial labeling errors , automates vial labeling, creates completely customizable vial identification, and dramatically increases sample throughput, up to 8X. This system increases efficiency for you chromatography analysis.
http://www.thermoscientific.com/en/product/virtuoso-vial-identification-system.html
Five Costly Mistakes with Water Quality Sondes Webinar Deck | YSI | EXOXylem Inc.
YSI reveals some of the most frequently seen mishaps in respect to water quality sonde calibrations, hardware setup, maintenance and more. This is the slide deck from the webinar help in December 2014.
Training and education can help alleviate these issues.
You can also view the recorded webinar by registering here: http://info.xyleminc.com/5-Costly-Mistakes-Webinar-Download-Recording.html
Gale Technologies Explains How to Streamline A Network LaboratoryGaletech
Gale Technologies explains how to streamline a network laboratory. This document also points out different ways of lab management & how Gale Technologies' network lab automation system can be both cost effective & error free.
Hand labeling tubes is time consuming and tedious. Laboratory automation will provide valuable walk away time to attend to other important tasks, reduce repetitive injuries, eliminate human error, and reduce costs in the lab.
Five Costly Mistakes with Water Quality Sondes Webinar Deck | YSI | EXOXylem Inc.
YSI reveals some of the most frequently seen mishaps in respect to water quality sonde calibrations, hardware setup, maintenance and more. This is the slide deck from the webinar help in December 2014.
Training and education can help alleviate these issues.
You can also view the recorded webinar by registering here: http://info.xyleminc.com/5-Costly-Mistakes-Webinar-Download-Recording.html
Gale Technologies Explains How to Streamline A Network LaboratoryGaletech
Gale Technologies explains how to streamline a network laboratory. This document also points out different ways of lab management & how Gale Technologies' network lab automation system can be both cost effective & error free.
Hand labeling tubes is time consuming and tedious. Laboratory automation will provide valuable walk away time to attend to other important tasks, reduce repetitive injuries, eliminate human error, and reduce costs in the lab.
WINGLO CLOUD BASED LIMS - Comprehensive Solutions for Small medium and Lar...Innowave Healthcare
INTRODUCTION
Winglo is a cloud-based healthcare IT Product company founded by a team
of professionals having rich techno-functional experience building product for some of the biggest Labs in the world that processes over 50 K
samples very day. Every feature of the product is a reflection of real-time
on-the-ground experience that was acquired over a period of 12 years
working for these labs.
Winglo’s WinLIMS is a cloud-based, multi-tenant solution built on the latest open-source technologies for stand-alone diagnostic Labs, Chain of
Labs and Diagnostic Labs within a Hospital. The cloud-based system can be
made accessible from anywhere, any time. WinLIMS covers the end-to-end
process of a Lab right from Patient Registration, Billing, Sample Collection,
Result Entry, Validation, Report Dispatch to all the internals of a Diagnostic
Laboratory.
Benefits of Cloud
• Reduce server/software maintenance cost
• Eliminates Software obsolescence
• Opportunity cost on servers and AMC spent
• Accessible to Lab Owners and Approving Doctors from Anywhere and
Anytime
• Eliminate printing and courier costs, saves emailing and messaging
time
• Increases overall productivity and TAT
• Software readiness to a new lab or collection center on Click of a Button
• Easy to support and maintain from Anywhere, anytime
• Seamless product upgrades
Part of the induction course for students undertaking diploma and degree in Analytical Chemistry, Applied Biology, Medical Lab Sciences and Food Technology.
Design and development of lateral flow assays for field useBrendan O'Farrell
Lateral flow assays are the most mature, stable, field deployable sensor available today. They can be used in myriad applications, from medical diagnostics to veterinary testing, agriculture, bio-defense, food testing and environmental testing, to name a few. Performance of these assays has evolved to the point where they can equal that of much more highly complex laboratory based diagnostic test formats. They can be quantitative, multiplexed and highly sensitive if developed and manufactured correctly. Design and development of these high performance lateral flow systems requires a from-first-principles approach, with an eye to optimizing the system for reproduciblity and sensitivity. Employing user - centered design and development practices greatly improves the odds of successful commercialization. DCN Diagnostics (formerly Diagnostic Consulting Network) develops high performance lateral flow assay systems for use in any environment. Our concurrent design and development process, employing cross functional teams of industrial design and mechanical engineers alongside our immunoassay development teams, ensures that the right product is developed the right way to allow for most efficient regulatory approval and commercialization. Our development process is fully design controlled and operates under our ISO 9001:2008 and EN 13485 compliant quality system. With literally hundreds of assays developed, and transferred to manufacturing, DCN is the go-to supplier of contract development services in the point of care diagnostic test market. Additionally, our consulting teams can provide a deep strategic vision to our clients, assisting in all aspects of product development and commercialization, including regulatory affairs and clinical trial management. This presentation describes DCN's development process and illustrates the benefit of a user centered design process in creating the right rapid assay for your market, focusing on field deployed tests for clinical diagnostics, veterinary testing and bio-defense applications. A variety of case studies are shown, illustrating the principles discussed.
Visual Inspection of Parentetal Drug Products in Pharmaceutical Quality testingKarishmaRK
This presentation aims to elaborate the regulatory & compendial requirements of Visual inspection in Pharmaceutical parenteral manufacturing and the methodology of carrying out the testing.
How often is Right for Laboratory Quality Control?Randox
Improving Laboratory Performance Through QC - How often is right for QC? Ask the Right Questions to get the Right Answers.
It is widely accepted that laboratories should perform QC at least every day of patient testing. However, is this adequate for every assay and for every laboratory? Is running QC once per day really sufficient? what is the "right" frequency for running QC samples in your laboratory?
Designing an appropriate QC procedure for your laboratoryRandox
Improving Laboratory Performance Through Quality Control - Five Simple Steps for QC Success.
It is easy to get caught up in an abundance of QC statistics and forget the fundamental reason why
QC exists in the first instance. QC is about detecting errors and ensuring that the results you
produce are accurate and reliable. All QC procedures should focus on reducing the risk of harm
to the patient. We are not examining statistics; we are examining real patients, real results and real
lives. Around 70% of all medical decisions are based on laboratory results, which is why it is of
utmost importance that each and every laboratory, has a well-designed QC procedure in place.
[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
This is a comprehensive set of checklists for waste-finding in manufacturing companies. The checklists are based on the eight types of Lean waste:
1. Overproduction
2. Inventory
3. Waiting
4. Motion
5. Transportation
6. Defects
7. Overprocessing
8. Intellectual
The checklists have a combined total of 65 waste items which could be potentially found on the shopfloor. For each checklist item, the magnitude of waste can be quantified under four levels:
Magnitude 0 : No waste found
Magnitude 1 : Very little waste
Magnitude 2 : Some waste
Magnitude 3 : A lot of waste
The checklists can be applied generally to all manufacturing departments. Users may adopt the checklists as they are, or customize them to suit your specific application. Add or delete the checklist items as needed.
The checklists form the basis of a structured improvement plan. Waste items can be ranked or prioritized and assigned to a person or team to develop an action plan for eliminating the identified waste within a certain timeframe.
CONTENTS:
1. Summary of the Eight Types of Lean Waste
2. Waste-finding Checklists
2.1 Waste-finding Checklist: Overproduction
2.2 Waste-finding Checklist: Inventory
2.3 Waste-finding Checklist: Waiting
2.4 Waste-finding Checklist: Motion
2.5 Waste-finding Checklist: Transportation
2.6 Waste-finding Checklist: Defects
2.7 Waste-finding Checklist: Overprocessing
2.8 Waste-finding Checklist: Intellectual
2.9 Major Waste-finding Checklist
March 5, 2015 PoCDx Seminar - Wallace White, Stratos - Development of the Pan...BerkeleyPoCDx
Development of the PanDx Integrated Diagnostic Platform
Wallace White
Director, Point-of-Care Diagnostics
Stratos Product Development
UC Berkeley, March 5, 2015
After a decade developing point-of-care diagnostics for commercial clients, Stratos Product Development was approached by the Bill and Melinda Gates Foundation for a bigger challenge: creating a single system capable of all the diagnostics needed at primary health clinics in developing countries. In this—the first public talk on the project—Wallace White will describe the development of the PanDx system and share observations from the health-clinic visits on three continents that have informed it.
Video of the talk is available on YouTube: https://www.youtube.com/watch?v=9oewE5NH4mI
Merging Cath Labs: Using simulation to design a solution and understand the i...SIMUL8 Corporation
Learn how Boston Scientific used simulation to test the impact of merging Cath Labs from two different sites in a Canadian hospital.
In this live webinar session, Boston Scientific's Yixin Wang will discuss how simulation formed a key part of the change process, engaged clinicians and administrators in the redesign, and ensured consensus on the best solution.
You'll learn how the teams worked together to understand the complexities of future demand from the local population, procedure types and timings, staffing, scheduling, as well as determining the optimum design for the combined unit.
This webinar will provide pesticides residue analysts with valuable information on software method development and data processing for the analysis of pesticide residues in food for both LC–MS and GC–MS. Technical experts will review the latest in software advances to help with data interpretation and reporting.
This presentation will focus on the new USP Chapter <2232> on elemental contaminants in dietary supplements. In particular, it will discuss the permitted daily exposure (PDE) limits of the four heavy metals of toxicological concern defined in the chapter and the different options for measurement strategies to meet these limits. In addition it will give an overview of the new USP Chapter <233>, which describes the suggested sample preparation, instrumental techniques and validation protocols required to demonstrate compliance of the analytical procedure used.
More Related Content
Similar to Chromatography: Virtuoso Vial Identification System
WINGLO CLOUD BASED LIMS - Comprehensive Solutions for Small medium and Lar...Innowave Healthcare
INTRODUCTION
Winglo is a cloud-based healthcare IT Product company founded by a team
of professionals having rich techno-functional experience building product for some of the biggest Labs in the world that processes over 50 K
samples very day. Every feature of the product is a reflection of real-time
on-the-ground experience that was acquired over a period of 12 years
working for these labs.
Winglo’s WinLIMS is a cloud-based, multi-tenant solution built on the latest open-source technologies for stand-alone diagnostic Labs, Chain of
Labs and Diagnostic Labs within a Hospital. The cloud-based system can be
made accessible from anywhere, any time. WinLIMS covers the end-to-end
process of a Lab right from Patient Registration, Billing, Sample Collection,
Result Entry, Validation, Report Dispatch to all the internals of a Diagnostic
Laboratory.
Benefits of Cloud
• Reduce server/software maintenance cost
• Eliminates Software obsolescence
• Opportunity cost on servers and AMC spent
• Accessible to Lab Owners and Approving Doctors from Anywhere and
Anytime
• Eliminate printing and courier costs, saves emailing and messaging
time
• Increases overall productivity and TAT
• Software readiness to a new lab or collection center on Click of a Button
• Easy to support and maintain from Anywhere, anytime
• Seamless product upgrades
Part of the induction course for students undertaking diploma and degree in Analytical Chemistry, Applied Biology, Medical Lab Sciences and Food Technology.
Design and development of lateral flow assays for field useBrendan O'Farrell
Lateral flow assays are the most mature, stable, field deployable sensor available today. They can be used in myriad applications, from medical diagnostics to veterinary testing, agriculture, bio-defense, food testing and environmental testing, to name a few. Performance of these assays has evolved to the point where they can equal that of much more highly complex laboratory based diagnostic test formats. They can be quantitative, multiplexed and highly sensitive if developed and manufactured correctly. Design and development of these high performance lateral flow systems requires a from-first-principles approach, with an eye to optimizing the system for reproduciblity and sensitivity. Employing user - centered design and development practices greatly improves the odds of successful commercialization. DCN Diagnostics (formerly Diagnostic Consulting Network) develops high performance lateral flow assay systems for use in any environment. Our concurrent design and development process, employing cross functional teams of industrial design and mechanical engineers alongside our immunoassay development teams, ensures that the right product is developed the right way to allow for most efficient regulatory approval and commercialization. Our development process is fully design controlled and operates under our ISO 9001:2008 and EN 13485 compliant quality system. With literally hundreds of assays developed, and transferred to manufacturing, DCN is the go-to supplier of contract development services in the point of care diagnostic test market. Additionally, our consulting teams can provide a deep strategic vision to our clients, assisting in all aspects of product development and commercialization, including regulatory affairs and clinical trial management. This presentation describes DCN's development process and illustrates the benefit of a user centered design process in creating the right rapid assay for your market, focusing on field deployed tests for clinical diagnostics, veterinary testing and bio-defense applications. A variety of case studies are shown, illustrating the principles discussed.
Visual Inspection of Parentetal Drug Products in Pharmaceutical Quality testingKarishmaRK
This presentation aims to elaborate the regulatory & compendial requirements of Visual inspection in Pharmaceutical parenteral manufacturing and the methodology of carrying out the testing.
How often is Right for Laboratory Quality Control?Randox
Improving Laboratory Performance Through QC - How often is right for QC? Ask the Right Questions to get the Right Answers.
It is widely accepted that laboratories should perform QC at least every day of patient testing. However, is this adequate for every assay and for every laboratory? Is running QC once per day really sufficient? what is the "right" frequency for running QC samples in your laboratory?
Designing an appropriate QC procedure for your laboratoryRandox
Improving Laboratory Performance Through Quality Control - Five Simple Steps for QC Success.
It is easy to get caught up in an abundance of QC statistics and forget the fundamental reason why
QC exists in the first instance. QC is about detecting errors and ensuring that the results you
produce are accurate and reliable. All QC procedures should focus on reducing the risk of harm
to the patient. We are not examining statistics; we are examining real patients, real results and real
lives. Around 70% of all medical decisions are based on laboratory results, which is why it is of
utmost importance that each and every laboratory, has a well-designed QC procedure in place.
[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
This is a comprehensive set of checklists for waste-finding in manufacturing companies. The checklists are based on the eight types of Lean waste:
1. Overproduction
2. Inventory
3. Waiting
4. Motion
5. Transportation
6. Defects
7. Overprocessing
8. Intellectual
The checklists have a combined total of 65 waste items which could be potentially found on the shopfloor. For each checklist item, the magnitude of waste can be quantified under four levels:
Magnitude 0 : No waste found
Magnitude 1 : Very little waste
Magnitude 2 : Some waste
Magnitude 3 : A lot of waste
The checklists can be applied generally to all manufacturing departments. Users may adopt the checklists as they are, or customize them to suit your specific application. Add or delete the checklist items as needed.
The checklists form the basis of a structured improvement plan. Waste items can be ranked or prioritized and assigned to a person or team to develop an action plan for eliminating the identified waste within a certain timeframe.
CONTENTS:
1. Summary of the Eight Types of Lean Waste
2. Waste-finding Checklists
2.1 Waste-finding Checklist: Overproduction
2.2 Waste-finding Checklist: Inventory
2.3 Waste-finding Checklist: Waiting
2.4 Waste-finding Checklist: Motion
2.5 Waste-finding Checklist: Transportation
2.6 Waste-finding Checklist: Defects
2.7 Waste-finding Checklist: Overprocessing
2.8 Waste-finding Checklist: Intellectual
2.9 Major Waste-finding Checklist
March 5, 2015 PoCDx Seminar - Wallace White, Stratos - Development of the Pan...BerkeleyPoCDx
Development of the PanDx Integrated Diagnostic Platform
Wallace White
Director, Point-of-Care Diagnostics
Stratos Product Development
UC Berkeley, March 5, 2015
After a decade developing point-of-care diagnostics for commercial clients, Stratos Product Development was approached by the Bill and Melinda Gates Foundation for a bigger challenge: creating a single system capable of all the diagnostics needed at primary health clinics in developing countries. In this—the first public talk on the project—Wallace White will describe the development of the PanDx system and share observations from the health-clinic visits on three continents that have informed it.
Video of the talk is available on YouTube: https://www.youtube.com/watch?v=9oewE5NH4mI
Merging Cath Labs: Using simulation to design a solution and understand the i...SIMUL8 Corporation
Learn how Boston Scientific used simulation to test the impact of merging Cath Labs from two different sites in a Canadian hospital.
In this live webinar session, Boston Scientific's Yixin Wang will discuss how simulation formed a key part of the change process, engaged clinicians and administrators in the redesign, and ensured consensus on the best solution.
You'll learn how the teams worked together to understand the complexities of future demand from the local population, procedure types and timings, staffing, scheduling, as well as determining the optimum design for the combined unit.
Similar to Chromatography: Virtuoso Vial Identification System (20)
This webinar will provide pesticides residue analysts with valuable information on software method development and data processing for the analysis of pesticide residues in food for both LC–MS and GC–MS. Technical experts will review the latest in software advances to help with data interpretation and reporting.
This presentation will focus on the new USP Chapter <2232> on elemental contaminants in dietary supplements. In particular, it will discuss the permitted daily exposure (PDE) limits of the four heavy metals of toxicological concern defined in the chapter and the different options for measurement strategies to meet these limits. In addition it will give an overview of the new USP Chapter <233>, which describes the suggested sample preparation, instrumental techniques and validation protocols required to demonstrate compliance of the analytical procedure used.
This webinar will provide pesticides residue analysts with valuable information on the development and optimization of gas chromatographic separations and mass spectrometry methods for the analysis of pesticide residues in food. The expert speakers will share their knowledge in understanding the critical points of the method, assisting analysts in modifying existing methods, and understanding instrumental and software technologies with the goal of improving laboratory productivity and reducing the overall cost per sample. The results of experiments for both screening and quantification workflows, using the latest technology, will be presented.
In this webinar Dr. Bertrand Rochat of Faculté de Biologie et de Médecine of the Centre Hospitalier Universitraire Vaudois (CHUV) at Lausanne discusses the paradigm shift to high resolution mass spectrometry (HRMS) in clinical research for quantitative analyses (sensitivity, selectivity, etc.). Quantifications in high resolution full scan or MS/MS mode will be compared with triple quadrupole MS. He will present Quan/Qual analysis with a study on the fate of an anti-cancer agent in human: with over 40 metabolites being identified and quantified; as well as metabolomics data underscoring the versatility of high resolution Orbitrap MS.
This webinar will provide pesticides residue analysts with valuable information on the development and optimization of chromatographic separations and mass spectrometry methods for the analysis of pesticide residues in food. The expert speakers will share their knowledge in understanding the critical aspects of the method, assisting analysts in optimizing their methods for the most challenging analyses.
Many factors impacting the measurement precision of ICP-OES and ICP-MS are still often neglected for everyday operation, however. Sample preparation is one of the factors that play a crucial role in the success of high-quality sample analysis. In this webinar, our experts will discuss sample preparation to: 1) improve analysis precision 2) make difficult samples easy to be analyzed 3) eliminate sample dilution to minimize error introduction.
For more information, please visit here: http://chrom.ms/CtRtKpw
Join the experts as they discuss the use of accelerated solvent extraction and QuEChERS techniques for the extraction of pesticide residues from a diverse range of food samples. Tips and tricks for improving the extraction efficiency will be covered, along with selection criteria for each technique by sample type, assisting analysts in modifying existing methods or developing new methods to tackle their analytical challenges
The webinar is all about Ultra High Pressure Liquid Chromatography (UHPLC) performance and how new column technology can deliver the best separation power and be married with the best UHPLC system to ensure an outstanding result. It covers how chromatographers can ensure that even very complex and unfamiliar samples are assayed with the highest scrutiny possible? The webinar discusses how to get the most out of solid core column technology with the right UHPLC system. It covers the use of an extremely long column approach for ultra-high resolution assays and the outlines the importance of robustness and retention time stability.
In the pharmaceutical arena there is great interest in solid core technology, where there is a broad range of sample types as well as requirements throughout the process of developing new chemical entities. The presentation looks at how solid core technology can be readily adapted to cope with the challenges associated with the pharmaceutical sector, looking at various sample matrices and molecular entities, from small molecules to large biomolecules. The presentation gives an insight into how varying the solid core to porous layer allows the user to optimize separation performance by reducing extra band broadening. Data presented demonstrates how this technology is more robust than fully porous systems when analyzing biological extracts, routinely used in DMPK departments, resulting in longer column lifetimes.
Stationary Phase and Mobile Phase Selection for Liquid Chromatography
The presentation focuses on how to choose the appropriate mode of separation, the correct column and highlights the importance of the correct mobile phase. This approach will be applied to a wide selection of compound types ranging from proteins, peptides, glycans to small pharmaceutical molecules and their metabolites. It will also look at specific application areas for monoclonal antibody analysis, namely: titer, aggregation, charge and oxidation variant. Platform methods for biologics characterization are also discussed.
Investigation into the design and application of solid core stationary phases has led to a better understanding of how the phases work and has resulted in their design aligned to the structure of the analytes being separated. The current range of columns available is discussed both in terms of selectivities, and also morphologies, allowing informed decisions to be made by the chromatographer. Using real life examples, coupled with advanced modeling, the effects of the particle size and morphology will be given for both small and large molecules, offering an insight into what the future holds for solid core products.
Over the past decade, the number of mAb candidates entering the clinical pipeline has grown significantly. In addition, the number of ADCs that use mAb specificity to carry drug payloads to target sites has increased. As a result, analytical characterization is in high demand.
This webinar discusses new innovations in sample preparation, column technology, UHPLC, and high resolution mass spectroscopy (HRMS) that allow the development of analytical methods with run times of less than 5 minutes for all routine methods.
Over the past decade, there have been a growing number of mAb candidates entering the clinical pipeline. This results in a large increase on the demand for analytical characterization. This seminar discusses advances in analytical method development with analytical run times below 10 minutes for all routine methods with intelligent, integrated chromatography workflows. Orbitrap technology has been established as the most powerful MS technology for protein characterization. How this can be incorporated into a complete workflow for bio-pharma analysis is also discussed.
Overview of webinar:
Rechargeable, manganese-based, lithium-ion batteries (LiBs) are environmentally friendly, have a good safety record, and can be made at a lower cost than other metal-based LiBs. However, they have a shorter lifetime. Much research has been spent on improving product safety, cycle life, and product performance, yet understanding fundamental processes and degradation mechanism in LiBs remains a challenge. Identifying breakdown products and understanding degradation processes can lead to enhancing battery performance, improvements in product safety, and insight into component failure mechanisms.
Analysis of Disinfection Byproducts by Ion Chromatography
In this presentation, the use of ion chromatography for the determination of bromate, chlorate and haloacetic acids for compliance monitoring according to various ISO standards (15061, 11206, 10304-4, 23631) and U.S. EPA Method 557 will be discussed. Examples will include IC methods using electrolytically generated hydroxide eluents on an RFIC™ system.
Determination of Common Counterions and Impurity Anions in Pharmaceuticals Using a Capillary HPIC System with Suppressed Conductivity and Charge Detection
Recently, identification and quantification of ions in early stage drug development has gained increasing attention, because the APIs maybe contaminated with different counter ions from synthesis steps, and because selecting the counter ion to enhance APIs’ solubility and stability is becoming a key step in formulation development. This presentation demonstrates the identification and quantification of 22 commonly found anions in pharmaceuticals in a single run using a high-pressure capillary IC system (HPIC) with 4-μm particle ion –exchange column, and CD-QD dual detectors.
Analysis of Anions and Cations in Produced Water from Hydraulic Fracturing Using Ion Chromatography
This presentation describes the use of ion chromatography (IC) to determine anions and cations in produced water from three different hydraulic fracturing sites. Considerable variation in ion concentration was found, which was attributed to differences in the geology of the locations from which samples were obtained.
Analysis of Cations in Hydraulic Fracturing Flowback Water from the Marcellus Shale Using Ion Chromatography
This presentation describes the determination of cations in hydraulic fracturing flowback water using ion chromatography. In this work, sodium was most abundant, followed by calcium, strontium, magnesium, potassium, barium, ammonium, and then lithium, respectively. The quantity of scale-forming ions, such as calcium, strontium, and barium, is particularly informative because it can be used to determine the amount of anti-scaling agent in fracturing fluid mix that will maximize hydrocarbon recovery.
Determination of Carbohydrates in Various Matrices by Capillary High-Performance Anion-Exchange Chromatography with Pulsed Amperometric Detection (HPAE-PAD)
This presentation describes the combined advantages of a reagent-free capillary format Ion Chromatography (IC) to determine monosaccharides and disaccharides in various applications, from low concentrations in synthetic urine samples to high concentrations in beverage samples. In a reagent-free IC system, the hydroxide eluent is electrolytically generated inline to deliver accurate and precise concentrations for isocratic or gradient separations by only adding deionized water. Eluent generation eliminates carbonate contamination and errors from manual preparation. A capillary scale system with µL/min flow rates can run 24/7, always on and always ready for samples.
High-performance anion-exchange chromatography with pulsed amperometric detection is valuable for oligosaccharide analysis with the value derived from the high-resolution separation followed by sensitive detection of native oligosaccharides. In this presentation the application of HPAE-PAD to oligosaccharides released from glycoproteins is demonstrated.
More from Chromatography & Mass Spectrometry Solutions (20)
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
3. 3
Or is this how you label your vial?
Hopefully so!
4. 4
How Important is Vial Labeling
“We’ve done some pretty clever things in the lab to minimize
sequencing errors, but this one still keeps me up at night. I’ve
asked everyone in the industry that I meet and all of our new
hires if they have any ideas and so far no one has offered
more than what we are currently doing.”
- CEO of a large environmental lab in US
6. 6
Vial Identification Workflow – 30,000ft
Vial
Sample
Marked Vial
Cap/Closure
Experiment
Type
Mark
Vial
Close
Vial
Storage Tray,
in a position
Autosampler
Determine and Enter Instrument
Sequence Data
Analysis
Add
Sample
Temp storage
Load
Sample Set
# - Individual
Identity
Marking Detail
Disposal
Long Term
Storage
UnLoad
Reference Data
7. 7
Situational Analysis
• Vial labeling manual & error prone
• Vial labeling is “expensive”, from the rework perspective
• Vial labeling has “no good” solution yet, and existing
solutions tend to be ad hoc
• Vial labeling is often ignored and is often abdicated to
the instrument autosampler sequence
• Rather than value add, it’s necessary evil
• Vial labeling is temporary & fragile
• Vial labeling is not automated or considered as part
workflow efficiency improvements
• Vial labeling detail is compromised by the methods used
for marking
• Vial labeling tends to be user specific “coding” & not
universal throughout a laboratory
• Vial labeling depends on human resources
8. 8
What vial labeling has become
• The manual nature of vial labeling, as it currently exists in
most laboratories, is error prone, time-consuming and does
not add value to the work flow
9. 9
Research tells us
• The average time it takes to manually label (handwritten or
paper label) is 39 seconds
• The average wage for a laboratory analyst is $29/hr
• A typical laboratory will label 80 vials per day
• Over 92 hours a year labeling vial
• Over $6,250 in labor spent vial labels
• It’s a BIG issue
12. 12
What is Virtuoso?
First of its kind vial identification system, that removes manual
vial labeling errors , automates vial labeling, creates
completely customizable vial identification, and dramatically
increases sample throughput, up to 8X.
14. 14
Virtuoso Benefits
• Facilitates Labeling Requirements
• Fully loaded with standard or fully user-defined templates
• Increases Productivity- Eliminate error-prone manual vial
labeling
• Label a vial in just 5 seconds
• Improve labeling efficiencies by downloading sample lists
• Simplify vial sample identification
• Produces High-Quality Labeling
• Resists common laboratory solvents, blurring, and smudging
• Provides an Advanced Labeling and information System in
One Device
• Designed by experienced analytical scientists
15. 15
Virtuoso - No smudge, no smear, no question
Thermo Scientific Virtuoso Vial Identification
System
• Create customizable vial identification directly on
vial
• Increase vial labelling through-put up to 8 times
• Improves confidence in data by removing
labelling errors