This document provides information about Phytronix, a company that offers multi-vendor analytical instrument services including repairs, maintenance, calibration, relocation, and advisory services. They service various types of analytical instruments from many manufacturers. They describe service options like banks of service hours or service agreements that provide guaranteed response times. They also discuss advisory services like consulting, laboratory design, method development, training, and performance verification to help customers select, set up, and optimize the use of analytical instruments.
Acusera Verify Linearity Verification - June 17 LT674Randox
Our Acusera Linearity Sets are perfect for laboratories wishing to challenge the full reportable range of their instruments. With sets available for Roche & Beckman analysers, our sets are sure to meet all your laboratory and regulatory requirements.
RIQAS is the largest international External Quality Assessment (EQA)/ Proficiency Testing (PT) scheme, there are currently more than 45,000 participants in 133 countries.
Quality Control for Point of Care Testing - White PaperRandox
Point of care testing (POCT) refers to testing that is performed near or at the site of a patient with the result leading to a possible change in the care of the patient. Over the past few years, the popularity and demand of POCT has been growing rapidly. This should come as no surprise as there are many advantages to POCT, for example, the added convenience of being able to obtain a rapid result at the patient’s bedside, thus allowing immediate action, saving time and improving the potential outcome for the patient.
Randox QC offer an extensive range of third party quality controls. Manufactured independently, the Acusera range delivers unbiased performance assessment with any instrument or method, helping to meet ISO 15189:2012 requirements whilst simultaneously eliminating the need for multiple instrument dedicated controls.
Dear Sir / Madam,
Greetings!
Stabicon with three and half years in niche Service provider segment, handling customer ranging from a sole proprietorship pharmaceutical consultancy to multinational pharmaceutical organization with several hundred employees, some of whom go out to perform anything from products manufacturing provider to complete product brand leaders. In course of business we have understood that laboratory activity costing evaluation is a major hurdle and create confusion at management level to take strategic partnering decision of routine Stability, Analytical, Formulation Development activity and etc. There is need for standardized costing model to evaluate in-house GLP regulatory Lab versus strategic partner GLP regulatory lab for activity costing. Please find the enclosed copy of HPLC-UV analysis costing model for Assay/Purity; Related Substances/Impurity/Degradation, Dissolution activity. This presentation will help in taking decision of partnering with specialized lab to support the long-term goals of your business.
We have other costing model available for Formulation Development, Microbiology Analysis ,Analytical Validation, Stability Storage and Complete product Analysis. Apart from these costing models, we also offer service based on Full Time Equivalent, Complete facility setting up and Operation Model.
Let us know if you would be interested in partnering with us with return email specifying area of interest to discuss further.
Attachment Link: HPLC COSTING
Thanks & Regards,
S. Sujin,
Team – Business Development
Email: Sujin@stabicon.com
Stabicon Life Sciences Pvt. Ltd.
Plot No. 28 l Bommasandra Industrial Area l 4th Phase l Jigani hobli l Anekal Taluk l Bangalore - 560 100 l India l
R&D Centre: +91 80 27839259/ 9260 l Corporate Office: +91 80 41285405 l Website: www.stabicon.com l
Accreditations: WHO | NABL | CDSCO | HEALTH CANADA |
About Us: Presentation | Outsourcing | Video | Route Map |
Think Green!!! Before printing this e-mail |
Acusera 24.7 is an interboratory data management software capable of automatically calculating measurement of uncertainty and six-sigma. With real time peer group updates and user friendly comprehensive charts and reports including Levey Jennings and histograms, our Acusera 24.7 software is now smarter, faster and more efficient than ever before!
Acusera Verify Linearity Verification - June 17 LT674Randox
Our Acusera Linearity Sets are perfect for laboratories wishing to challenge the full reportable range of their instruments. With sets available for Roche & Beckman analysers, our sets are sure to meet all your laboratory and regulatory requirements.
RIQAS is the largest international External Quality Assessment (EQA)/ Proficiency Testing (PT) scheme, there are currently more than 45,000 participants in 133 countries.
Quality Control for Point of Care Testing - White PaperRandox
Point of care testing (POCT) refers to testing that is performed near or at the site of a patient with the result leading to a possible change in the care of the patient. Over the past few years, the popularity and demand of POCT has been growing rapidly. This should come as no surprise as there are many advantages to POCT, for example, the added convenience of being able to obtain a rapid result at the patient’s bedside, thus allowing immediate action, saving time and improving the potential outcome for the patient.
Randox QC offer an extensive range of third party quality controls. Manufactured independently, the Acusera range delivers unbiased performance assessment with any instrument or method, helping to meet ISO 15189:2012 requirements whilst simultaneously eliminating the need for multiple instrument dedicated controls.
Dear Sir / Madam,
Greetings!
Stabicon with three and half years in niche Service provider segment, handling customer ranging from a sole proprietorship pharmaceutical consultancy to multinational pharmaceutical organization with several hundred employees, some of whom go out to perform anything from products manufacturing provider to complete product brand leaders. In course of business we have understood that laboratory activity costing evaluation is a major hurdle and create confusion at management level to take strategic partnering decision of routine Stability, Analytical, Formulation Development activity and etc. There is need for standardized costing model to evaluate in-house GLP regulatory Lab versus strategic partner GLP regulatory lab for activity costing. Please find the enclosed copy of HPLC-UV analysis costing model for Assay/Purity; Related Substances/Impurity/Degradation, Dissolution activity. This presentation will help in taking decision of partnering with specialized lab to support the long-term goals of your business.
We have other costing model available for Formulation Development, Microbiology Analysis ,Analytical Validation, Stability Storage and Complete product Analysis. Apart from these costing models, we also offer service based on Full Time Equivalent, Complete facility setting up and Operation Model.
Let us know if you would be interested in partnering with us with return email specifying area of interest to discuss further.
Attachment Link: HPLC COSTING
Thanks & Regards,
S. Sujin,
Team – Business Development
Email: Sujin@stabicon.com
Stabicon Life Sciences Pvt. Ltd.
Plot No. 28 l Bommasandra Industrial Area l 4th Phase l Jigani hobli l Anekal Taluk l Bangalore - 560 100 l India l
R&D Centre: +91 80 27839259/ 9260 l Corporate Office: +91 80 41285405 l Website: www.stabicon.com l
Accreditations: WHO | NABL | CDSCO | HEALTH CANADA |
About Us: Presentation | Outsourcing | Video | Route Map |
Think Green!!! Before printing this e-mail |
Acusera 24.7 is an interboratory data management software capable of automatically calculating measurement of uncertainty and six-sigma. With real time peer group updates and user friendly comprehensive charts and reports including Levey Jennings and histograms, our Acusera 24.7 software is now smarter, faster and more efficient than ever before!
QC Multi rules - Improving Laboratory Performance Through Quality ControlRandox
Randox Quality Control's latest educational guide examines and explains what QC Multi-Rules are, How to identify an out of control event with QC rules, How to use QC Multi-Rules, The different types of analytical errors, The tools to assist labs and how a lab can troubleshoot QC errors.
this is just a review of Quality Control Scheme integrated by Dr Westgard and his son, as here in ordinary clinic lab that QA Scheme is followed, and the LH 500 and our ACT5 Diff Coulter Counter, we are able to get the Yearly Sigma Scale performance for each analytes, our TAE for each analytes, I compute based on Rico's accepted biological variation as I deemed it is much pertinent, thus the EQAS in the peer group, cumulative bias average for 6 months and the IQAS's LJ Chart has the CV%. The two instruments are well maintained , with carryover check for each modes, Accuracy / Precision Check By the Engineer, the Calibration, is always Passed the required threshold for each parameter.
This powerpoint presentation is graciously dedicated to the father and son, the WESTGARDS...we owe you this quality assurance for each instruments we have, either in Biochem or Hematology, we salute you and more power, God Bless. From Sis Rina, our simple JPC lab here in the Gulf--thanks so much!
Acusera Third Party Quality Controls for Medical Laboratories Randox
With over 350 parameters available in our Acusera range, choice and flexibility is guaranteed. Moreover the availability of truly independent third party controls coupled with the added advantages of highly accurate target values, increased stability and unparalleled quality will optimise performance, save valuable time and minimise waste in any laboratory.
Our comprehensive range of multi-analyte controls have been uniquely developed with ease of use in mind, combining up to 100 parameters in one convenient control laboratories can significantly reduce the need for multiple, costly single analyte controls.
Consolidation
100% human controls for immunoassay purposes
Most accurate target values
Unrivalled stability
Most consistent controls
True third party controls
Improving Laboratory Performance Through Quality Control - The role of EQA in...Randox
Randox Quality Control's five simple steps to QC success. The second education guide from Randox QC for clinical laboratory staff. The guide will examine how EQA works, benefits of EQA and what a laboratory should look for when choosing an EQA scheme.
Using Fusion QbD as an Analytical Quality by Design Software for Method Devel...Waters Corporation
This presentation describes the benefits of a hardware and software platform that dramatically advances LC and LC-MS method development by applying Analytical Quality by Design (AQbD) approaches in a 100% regulatory compliance supported framework. This AQbD aligned platform includes Waters Empower™ Chromatography Data System Software with enhanced Fusion QbD® Software, the Waters® ACQUITY UPLC H-Class PLUS, a PDA detector, and QDa Mass Detector. New software capabilities that optimize and simplify the use of mass detection in the AQbD method development workflow have been added.
Visit methods.waters.com for more information
The laboratory shall determine measurement uncertainty for each measurement procedure,
in the examination phases used to report measured quantity values on patients’ samples. The
laboratory shall define the performance requirements for the measurement uncertainty of each
measurement procedure and regularly review estimates of measurement uncertainty.
Modern liquid chromatography hardware and software embrace larger parts of our laboratory workflows than ever before. From sample preparation to sample vial labeling, from setting-up Liquid Chromatography runs to instant result calculation – everywhere along the workflow software and hardware automate work steps which have required manual action before. Next to better productivity, the automation and improved technologies also result in enhanced quality and result consistency.
The seminar reviews very practical examples which all users can relate too. It covers an attractive variety of application areas and analytical challenges.
Monitoring External Quality Assessment / Proficiency Testing Performance - Investigating the source of the problem.
In order to identify the source of the problem it is useful to be aware of the most common causes of poor EQA performance. Errors can occur at any
stage of the testing process however EQA is most concerned with detecting analytical errors i.e. errors that occur during the analysis of the sample.
Most analytical errors can be easily divided into three main areas; clerical errors, systematic errors and random errors. Systematic errors result in
inaccurate results that consistently show a positive or negative bias. Random errors on the other hand affect precision and result in fluctuations in
either direction.
Understanding The Process and Benefits of Proficiency Testing - Steve HepburnMara International
The 3rd GCC Laboratory Proficiency Conference is organized as part of the strategic orientations of the GCC Standardization
Organization (GSO) for the development of the standardization and quality infrastructure, thereby contributing to the development of commerce and industry and to the support of national economy in the GCC member states.
Since the field of proficiency testing is newly introduced in the GCC member states and as the infrastructure of laboratories has not yet taken the shape of national or regional organizations representing the laboratories and reflecting their requirements, GSO is in need of meeting with a considerable group of laboratories to explore and prioritize GCC member states’ requirements in terms of the fields which must top the list of the fields to be developed and upgraded.
Based on the study conducted by GSO during 2011 on the status of proficiency testing activities in the member states which shown that the laboratories operating in the member states are in need of a unified data center on proficiency testing activities, GSO
organized two conferences in 2013 and 2014 on the subject. The conferences scored high rates of success in terms of the selected scientific material, quality of speakers and the targeted audience.
Accordingly, GSO conceptualization of the method of coordinating and upgrading the activity of proficiency tests in the GCC member states included a recommendation on the organization of annual training courses and awareness symposia by the GSO on the fields of proficiency tests.
This year’s Conference will be held in Dubai during two days the 24th and 25th of March 2015, and will coincide with the annual Analytical Industry exhibition ARABLAB which will be held in Dubai during the period 23 – 26 March 2015.
Today’s laboratories want more from their liquid chromatography system: Higher performance. Better reliability. More consistent and comprehensive analytical workflows. And most of all, more predictable and reproducible results. At the same time, you want
As we have seen with the advent of the shale oil revolution in the United States, the development of new technology plays an important role in the oil and gas industry. It’s an enabler in reducing capital costs, simplifying production and increasing capacity of new or existing facilities. It can make a marginal project into a profitable development.
Progressing technology, while dealing with significant risk, is a challenge that can be overcome through a technology qualification process. A Technology Qualification Program (TQP) provides a means to identifying the risks and taking the correct steps to mitigate it; not avoid it.
This lecture summarizes the required steps involved in qualifying technology and how to keep track of technology development through the Technology Readiness Level (TRL) ranking system. In addition, some of the pitfalls in executing a TQP program are identified and discussed with emphasis on both component and system testing. Examples are given to illustrate the danger in taking shortcuts when executing the qualification plan.
Data from a recent subsea separation qualification program is presented comparing test results between CFDs, model fluid and actual crude testing at operating conditions. Knowing the limitations of the tools and testing system selected is an important step in closing the gaps identified in the TQP program.
The TRL has evolved at a faster pace and has become more acceptable in the oil and gas industry then the TQP. Nonetheless, continued standardization of both the TQP and TRL is still necessary in order to reduce overall cost of developing technology and allow faster implementation.
GPTS, PT provider from India, has designed ppt presentation on Overview of Proficiency testing to guide employees of testing laboratories and manufacturing companies about PT services. The topics covers in the presentation slides are what is PT, Why it requires, Elements of pt and Proficiency testing process etc.
QC Multi rules - Improving Laboratory Performance Through Quality ControlRandox
Randox Quality Control's latest educational guide examines and explains what QC Multi-Rules are, How to identify an out of control event with QC rules, How to use QC Multi-Rules, The different types of analytical errors, The tools to assist labs and how a lab can troubleshoot QC errors.
this is just a review of Quality Control Scheme integrated by Dr Westgard and his son, as here in ordinary clinic lab that QA Scheme is followed, and the LH 500 and our ACT5 Diff Coulter Counter, we are able to get the Yearly Sigma Scale performance for each analytes, our TAE for each analytes, I compute based on Rico's accepted biological variation as I deemed it is much pertinent, thus the EQAS in the peer group, cumulative bias average for 6 months and the IQAS's LJ Chart has the CV%. The two instruments are well maintained , with carryover check for each modes, Accuracy / Precision Check By the Engineer, the Calibration, is always Passed the required threshold for each parameter.
This powerpoint presentation is graciously dedicated to the father and son, the WESTGARDS...we owe you this quality assurance for each instruments we have, either in Biochem or Hematology, we salute you and more power, God Bless. From Sis Rina, our simple JPC lab here in the Gulf--thanks so much!
Acusera Third Party Quality Controls for Medical Laboratories Randox
With over 350 parameters available in our Acusera range, choice and flexibility is guaranteed. Moreover the availability of truly independent third party controls coupled with the added advantages of highly accurate target values, increased stability and unparalleled quality will optimise performance, save valuable time and minimise waste in any laboratory.
Our comprehensive range of multi-analyte controls have been uniquely developed with ease of use in mind, combining up to 100 parameters in one convenient control laboratories can significantly reduce the need for multiple, costly single analyte controls.
Consolidation
100% human controls for immunoassay purposes
Most accurate target values
Unrivalled stability
Most consistent controls
True third party controls
Improving Laboratory Performance Through Quality Control - The role of EQA in...Randox
Randox Quality Control's five simple steps to QC success. The second education guide from Randox QC for clinical laboratory staff. The guide will examine how EQA works, benefits of EQA and what a laboratory should look for when choosing an EQA scheme.
Using Fusion QbD as an Analytical Quality by Design Software for Method Devel...Waters Corporation
This presentation describes the benefits of a hardware and software platform that dramatically advances LC and LC-MS method development by applying Analytical Quality by Design (AQbD) approaches in a 100% regulatory compliance supported framework. This AQbD aligned platform includes Waters Empower™ Chromatography Data System Software with enhanced Fusion QbD® Software, the Waters® ACQUITY UPLC H-Class PLUS, a PDA detector, and QDa Mass Detector. New software capabilities that optimize and simplify the use of mass detection in the AQbD method development workflow have been added.
Visit methods.waters.com for more information
The laboratory shall determine measurement uncertainty for each measurement procedure,
in the examination phases used to report measured quantity values on patients’ samples. The
laboratory shall define the performance requirements for the measurement uncertainty of each
measurement procedure and regularly review estimates of measurement uncertainty.
Modern liquid chromatography hardware and software embrace larger parts of our laboratory workflows than ever before. From sample preparation to sample vial labeling, from setting-up Liquid Chromatography runs to instant result calculation – everywhere along the workflow software and hardware automate work steps which have required manual action before. Next to better productivity, the automation and improved technologies also result in enhanced quality and result consistency.
The seminar reviews very practical examples which all users can relate too. It covers an attractive variety of application areas and analytical challenges.
Monitoring External Quality Assessment / Proficiency Testing Performance - Investigating the source of the problem.
In order to identify the source of the problem it is useful to be aware of the most common causes of poor EQA performance. Errors can occur at any
stage of the testing process however EQA is most concerned with detecting analytical errors i.e. errors that occur during the analysis of the sample.
Most analytical errors can be easily divided into three main areas; clerical errors, systematic errors and random errors. Systematic errors result in
inaccurate results that consistently show a positive or negative bias. Random errors on the other hand affect precision and result in fluctuations in
either direction.
Understanding The Process and Benefits of Proficiency Testing - Steve HepburnMara International
The 3rd GCC Laboratory Proficiency Conference is organized as part of the strategic orientations of the GCC Standardization
Organization (GSO) for the development of the standardization and quality infrastructure, thereby contributing to the development of commerce and industry and to the support of national economy in the GCC member states.
Since the field of proficiency testing is newly introduced in the GCC member states and as the infrastructure of laboratories has not yet taken the shape of national or regional organizations representing the laboratories and reflecting their requirements, GSO is in need of meeting with a considerable group of laboratories to explore and prioritize GCC member states’ requirements in terms of the fields which must top the list of the fields to be developed and upgraded.
Based on the study conducted by GSO during 2011 on the status of proficiency testing activities in the member states which shown that the laboratories operating in the member states are in need of a unified data center on proficiency testing activities, GSO
organized two conferences in 2013 and 2014 on the subject. The conferences scored high rates of success in terms of the selected scientific material, quality of speakers and the targeted audience.
Accordingly, GSO conceptualization of the method of coordinating and upgrading the activity of proficiency tests in the GCC member states included a recommendation on the organization of annual training courses and awareness symposia by the GSO on the fields of proficiency tests.
This year’s Conference will be held in Dubai during two days the 24th and 25th of March 2015, and will coincide with the annual Analytical Industry exhibition ARABLAB which will be held in Dubai during the period 23 – 26 March 2015.
Today’s laboratories want more from their liquid chromatography system: Higher performance. Better reliability. More consistent and comprehensive analytical workflows. And most of all, more predictable and reproducible results. At the same time, you want
As we have seen with the advent of the shale oil revolution in the United States, the development of new technology plays an important role in the oil and gas industry. It’s an enabler in reducing capital costs, simplifying production and increasing capacity of new or existing facilities. It can make a marginal project into a profitable development.
Progressing technology, while dealing with significant risk, is a challenge that can be overcome through a technology qualification process. A Technology Qualification Program (TQP) provides a means to identifying the risks and taking the correct steps to mitigate it; not avoid it.
This lecture summarizes the required steps involved in qualifying technology and how to keep track of technology development through the Technology Readiness Level (TRL) ranking system. In addition, some of the pitfalls in executing a TQP program are identified and discussed with emphasis on both component and system testing. Examples are given to illustrate the danger in taking shortcuts when executing the qualification plan.
Data from a recent subsea separation qualification program is presented comparing test results between CFDs, model fluid and actual crude testing at operating conditions. Knowing the limitations of the tools and testing system selected is an important step in closing the gaps identified in the TQP program.
The TRL has evolved at a faster pace and has become more acceptable in the oil and gas industry then the TQP. Nonetheless, continued standardization of both the TQP and TRL is still necessary in order to reduce overall cost of developing technology and allow faster implementation.
GPTS, PT provider from India, has designed ppt presentation on Overview of Proficiency testing to guide employees of testing laboratories and manufacturing companies about PT services. The topics covers in the presentation slides are what is PT, Why it requires, Elements of pt and Proficiency testing process etc.
El Museo Arqueológico de Puente Genil ubicado en el antiguo convento de "La Victoria" datado del siglo XVII. El museo abrió sus puertas en el año 1991, desde esa fecha se llevan a cabo trabajos de restauración, exposición y divulgación de un Patrimonio histórico artístico de la localidad pontanense.
With deep industry knowledge, OneSource addresses your lab requirements to help optimize your business outcomes, delivering everything from
everyday instrument repair to data integrity services. OneSource takes a one-of-kind managed approach, utilizing a powerful, interwoven suite of
solutions including analytics, compliance, laboratory computing, scientific lab support, asset management, lab relocation, and other services.
DCN Diagnostics. Design and Development of Lateral Flow Assay SystemsBrendan O'Farrell
DCN Diagnostics designs and develops rapid assay systems for medical and veterinary diagnostics, bio-defense, agriculture, environmental testing and other market segments. DCN's service offering includes contract assay development, education and training courses in lateral flow technologies, industrial design and mechanical engineering services related to development of related devices for rapid diagnostics. Our specialties include lateral flow, flow through and microfluidic assay formats, and we have developed qualitative, quantitative, visual or fluorescent assay systems. DCN's ISO 9001:228 and EN 13485 compliant quality system is set up to allow us to deliver the full FDA compliant design history file. Our process and unique teams of highly experienced development scientists working alongside our engineering teams allow us to deliver the product, not just the parts. DCN Diagnostics is the sole supplier of cellulose nanobead technology for lateral flow diagnostics outside of Japan and can supply technical consulting and development assistance to companies wishing to develop and manufacture highly sensitive and quantitative lateral flow assays using the NanoAct (tm) beads. Our experience in multiplexing and joint ownership in the Symbolics patents covering aspects of multipex arraying in lateral flow formats allows DCN to assist our clients in creating highly unique and functional assays for any environment or application. DCN also provides our unique UltraGold (tm) colloidal gold for use in lateral flow assays. DCN's 40nm gold colloid is highly controlled, very stable and designed specifically for use in lateral flow and flow through assays.
Evolution Measurement are leading suppliers of measurement solutions. Covering Electrical, Temperature and Pressure measurement. Our experienced Engineers can develop, build, supply and install bespoke solutions specific to your measurement needs.
This presentation covers the benefits of an automated calibration system and how we can help you.
Modern business drivers are continually pushing to reduce the time it takes to get a product or service to market, reduce the risk and cost associated with that, and to improve quality.
In laboratories, delivering an analytical result that’s ‘right first time’ (RFT) is the answer. There is no reprocessing data or re-running injections and no out of specification (OOS) results or reporting/calculation errors.
Using chromatography data system tools for RFT analysis automatically gives high quality of results and confidence in results, lower cost of analysis, improved lab efficiency, and faster release to market and return on investment (ROI).
For more than 25 years, Applied Systems has been engaged in international projects devoted to the development of high-end measurement and test systems as well as customizable visualization software.
Our profound experience in industrial automation along with proven development techniques allow us to create solutions that are tailored to meet every client’s need.
For more than 25 years, Applied Systems has been engaged in international projects devoted to the development of high-end measurement and test systems as well as customizable visualization software.
Our profound experience in industrial automation along with proven development techniques allow us to create solutions that are tailored to meet every client’s need
Learn about a1-cbiss' refrigeration solutions that cover everything from refrigerant leak detection and monitoring through to emissions control in this brochure
3.0 Project 2_ Developing My Brand Identity Kit.pptxtanyjahb
A personal brand exploration presentation summarizes an individual's unique qualities and goals, covering strengths, values, passions, and target audience. It helps individuals understand what makes them stand out, their desired image, and how they aim to achieve it.
Cracking the Workplace Discipline Code Main.pptxWorkforce Group
Cultivating and maintaining discipline within teams is a critical differentiator for successful organisations.
Forward-thinking leaders and business managers understand the impact that discipline has on organisational success. A disciplined workforce operates with clarity, focus, and a shared understanding of expectations, ultimately driving better results, optimising productivity, and facilitating seamless collaboration.
Although discipline is not a one-size-fits-all approach, it can help create a work environment that encourages personal growth and accountability rather than solely relying on punitive measures.
In this deck, you will learn the significance of workplace discipline for organisational success. You’ll also learn
• Four (4) workplace discipline methods you should consider
• The best and most practical approach to implementing workplace discipline.
• Three (3) key tips to maintain a disciplined workplace.
Accpac to QuickBooks Conversion Navigating the Transition with Online Account...PaulBryant58
This article provides a comprehensive guide on how to
effectively manage the convert Accpac to QuickBooks , with a particular focus on utilizing online accounting services to streamline the process.
Attending a job Interview for B1 and B2 Englsih learnersErika906060
It is a sample of an interview for a business english class for pre-intermediate and intermediate english students with emphasis on the speking ability.
As a business owner in Delaware, staying on top of your tax obligations is paramount, especially with the annual deadline for Delaware Franchise Tax looming on March 1. One such obligation is the annual Delaware Franchise Tax, which serves as a crucial requirement for maintaining your company’s legal standing within the state. While the prospect of handling tax matters may seem daunting, rest assured that the process can be straightforward with the right guidance. In this comprehensive guide, we’ll walk you through the steps of filing your Delaware Franchise Tax and provide insights to help you navigate the process effectively.
India Orthopedic Devices Market: Unlocking Growth Secrets, Trends and Develop...Kumar Satyam
According to TechSci Research report, “India Orthopedic Devices Market -Industry Size, Share, Trends, Competition Forecast & Opportunities, 2030”, the India Orthopedic Devices Market stood at USD 1,280.54 Million in 2024 and is anticipated to grow with a CAGR of 7.84% in the forecast period, 2026-2030F. The India Orthopedic Devices Market is being driven by several factors. The most prominent ones include an increase in the elderly population, who are more prone to orthopedic conditions such as osteoporosis and arthritis. Moreover, the rise in sports injuries and road accidents are also contributing to the demand for orthopedic devices. Advances in technology and the introduction of innovative implants and prosthetics have further propelled the market growth. Additionally, government initiatives aimed at improving healthcare infrastructure and the increasing prevalence of lifestyle diseases have led to an upward trend in orthopedic surgeries, thereby fueling the market demand for these devices.
What is the TDS Return Filing Due Date for FY 2024-25.pdfseoforlegalpillers
It is crucial for the taxpayers to understand about the TDS Return Filing Due Date, so that they can fulfill your TDS obligations efficiently. Taxpayers can avoid penalties by sticking to the deadlines and by accurate filing of TDS. Timely filing of TDS will make sure about the availability of tax credits. You can also seek the professional guidance of experts like Legal Pillers for timely filing of the TDS Return.
Putting the SPARK into Virtual Training.pptxCynthia Clay
This 60-minute webinar, sponsored by Adobe, was delivered for the Training Mag Network. It explored the five elements of SPARK: Storytelling, Purpose, Action, Relationships, and Kudos. Knowing how to tell a well-structured story is key to building long-term memory. Stating a clear purpose that doesn't take away from the discovery learning process is critical. Ensuring that people move from theory to practical application is imperative. Creating strong social learning is the key to commitment and engagement. Validating and affirming participants' comments is the way to create a positive learning environment.
Premium MEAN Stack Development Solutions for Modern BusinessesSynapseIndia
Stay ahead of the curve with our premium MEAN Stack Development Solutions. Our expert developers utilize MongoDB, Express.js, AngularJS, and Node.js to create modern and responsive web applications. Trust us for cutting-edge solutions that drive your business growth and success.
Know more: https://www.synapseindia.com/technology/mean-stack-development-company.html
Unveiling the Secrets How Does Generative AI Work.pdfSam H
At its core, generative artificial intelligence relies on the concept of generative models, which serve as engines that churn out entirely new data resembling their training data. It is like a sculptor who has studied so many forms found in nature and then uses this knowledge to create sculptures from his imagination that have never been seen before anywhere else. If taken to cyberspace, gans work almost the same way.
RMD24 | Debunking the non-endemic revenue myth Marvin Vacquier Droop | First ...BBPMedia1
Marvin neemt je in deze presentatie mee in de voordelen van non-endemic advertising op retail media netwerken. Hij brengt ook de uitdagingen in beeld die de markt op dit moment heeft op het gebied van retail media voor niet-leveranciers.
Retail media wordt gezien als het nieuwe advertising-medium en ook mediabureaus richten massaal retail media-afdelingen op. Merken die niet in de betreffende winkel liggen staan ook nog niet in de rij om op de retail media netwerken te adverteren. Marvin belicht de uitdagingen die er zijn om echt aansluiting te vinden op die markt van non-endemic advertising.
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2. OUR VISION
Becoming the Canadian Leader
in analytical instrumentation and
the World Leader in high-throughput
analysis by mass spectrometry.
Our Mission
Providing exceptional products
and services in analytical
instrumentation to ensure that
our customers get better and
faster results.
3. MULTI-VENDOR SERVICE
Phytronix offers comprehensive repair and maintenance services for all of your laboratory instruments.
Our multidisciplinary team has in-depth knowledge and technical expertise to perform all analytical
instrument repairs with a fast on-site response time and at a competitive price.
Our multi-vendor services can provide:
Maintenance
Installation Evaluation Repairs Calibration
Laboratory
relocation
Performance
verification
On most types of laboratory
Instruments, such as:
• Mass spectrometers
• Chromatographs
• Mechanical pumps
• Gas generators
• Fumehoods
• Spectrophotometers
• Spectrometers
• Microplate readers
• Imagers
For most manufacturers,
such as:
• CTC Analytics
• Molecular Devices®
• Agilent® Technologies
• Waters® Corporation
• Thermo Scientific®
• Sciex™
• Shimadzu™
• Bruker Daltonics®
• Edwards Vacuum
• ADS Laminaire
• F-DGSi
• PEAK Scientific
4. 4 • Phytronix
YOUR SERVICE OPTIONS
In order to maintain your analytical instrumentation in optimal working order, we focus on your
specific requirements and will work with you to determine which service option is the best fit.
Supplementing our everyday “On-Call Repair” option, we can offer various contracts to meet your needs:
Bank Of Service
Hours
Bank of Service
Hours - Combo
Service
Agreement
Response
Time
Guaranteed
On-Site-Response
(24 hours, 48 hours)
Guaranteed
On-Site-Response
(24 hours, 48 hours)
Guaranteed
On-Site-Response
(24 hours, 48 hours)
Hours Bank of Hours
(100, 200, 300,…)
Bank of Hours
(100, 200, 300,…)
Unlimited
Duration Until the hours
are spent
Until the hours
are spent
1 year
Instruments
Covered
All All Specified on Contract
Parts Ordered by customer
or billable
Ordered by Phytronix
and charged to your
Combo account
Included
Preventive
Maintenance
As Needed
(Parts Billable)
As Needed
(Parts charged to
yourCombo account)
Included–Specified
on Contract
5. FAQ’S
You hesitate between the Bank of service hours or the service agreement, here are some frequently
asked questions and answers to guide your decision.
What Type of Agreements do You Offer?
Phytronix offers either Bank of Service Hours or Service Agreement the equivalent to a manufacturer
service contract for a competitive price.
What is a Bank of Service Hours?
Prepaid hours with a guaranteed response time used to cover all repairs and/or maintenance
of your analytical instrumentation, regardless of manufacturer or age of your equipment.
Which Instruments are Covered?
All analytical instruments from all manufacturers can be covered with your Bank of Service Hours.
With the service agreement, only specified instruments are covered and it is not offered for all
manufacturers.
What is the Response Time?
Both contract options have a standard 48 hours guaranteed On-Site-Response. However, 24 hours
response time is available.
What is the Agreement Duration?
A Bank of Service Hours contract has no time limitation, the agreement ends when all hours are spent.
The Service Agreement is usually valid for 1 year, unless otherwise specified in the contract.
Are the Parts Included?
Defective parts are covered by the Service Agreement. Consumables are not included. For the Bank
of Service Hours, a Combo Option can be added to accelerate the ordering of parts. The Combo is an
amount prepaid to Phytronix that can be used to order defective or consumables parts. This amount
can be converted into bank hours at any time.
6. 6 • Phytronix
ADVISORY SERVICES
Use our experience to your advantage! We can lead your choice to the right instrument, prepare your
laboratory for your new acquisition, help with the method development and train your end users.
CONSULTING
We can offer strategic insights for selection, delivery and implementation of new or used analytical
instrumentation into your lab. Make the right instrumental choice to meet your budgetary and
technical needs by comparing equipment’s specifications, price and advantages:
• Single Quadrupole (SQ) or Time of Flight (TOF)
• QTOF or Orbitrap
• Triple Quadrupole (TQ) w/ or w/o ion mobility
• UPLC or HPLC
• ITEX or P&T
• Pressure swing (PSA) or membrane gas generator
• Chemical Hood or Safety Cabinet
LABORATORY DESIGN
We can provide recommendations for setting up your laboratory or any infrastructure design
planning around your choice of instruments. Over the last decade, Phytronix has designed several
’top-of-the-line’ laboratories. Our experienced team of engineers can manage your laboratory design
and relocation needs.
LABORATORY PLANNING AND DESIGN
• Planning and Consultation
• Construction Site Supervision
• Laboratory instrument installation (GC, GC-MS, LC, LC-MS, ICP, ICP-MS)
• Uninterruptable Power Supply (UPS) implementation for analytical instruments
LABORATORY RELOCATION
• Instrument Verification Before and After Relocation
• Professional Preventative Maintenance, De-Installation and Packaging
• Qualified Monitoring of the Relocation Process
• Temporary storage available if necessary
7. METHOD DEVELOPMENT
Our team of experienced Chemists will help you develop robust analytical methods for your new
or existing instrumentation. From optimizing your sample preparation to in-depth instrument
and application support, our dedicated team will provide a tangible advantage to your laboratory.
• Extraction method (Liquid-Liquid, solid phase extraction, protein precipitation)
• Analytical method (LC-MS, GC-MS, HPLC, GC, ITEX)
• Automation method (Dilution, Derivatization, STD addition)
TRAINING
We offer personalized courses to help your team acquire theoretical and practical training on any
advanced analytical instrumentation. Phytronix offers courses in Mass Spectrometry and on most
separation techniques used in the laboratory.
The courses are designed to correspond to your specific needs and can be adapted in duration
and group size.
• Theoretical (Mass spectrometry, Chromatography, Vaccum techniques)
• Maintenance (LC-MS, GC-MS, HPLC, GC)
• User (Operation, Guideline, Software)
PERFORMANCE VERIFICATION (PV)
Complying with a GxP environment can be difficult when analytical instruments are involved.
One solution to reduce this complexity for Qualifications (OQ, PQ) is to harmonize your processes
by developing one generic protocol regardless of manufacturer. A single Standard Operation
Procedure (SOP) to verify your instruments performance will give your laboratory advantages such as:
simple control, easy to manage, and maximize confidence during audit.
We build your Performance Verification (PV) according to governmental instances and
your particular needs:
• Chromatographs (HPLC, UPLC, GC)
• Mass spectrometers (LC-MS & GC-MS)
8. 8 • Phytronix
Phytronix Instruments Inc.
Montréal Area
4975, Ambroise-Lafortune, Suite 100
Boisbriand (Québec) Canada J7H 0A4
P 450 419-6415 F 844 891-2549
Toronto Area (GTA)
3, Summerland Terrace, Suite 1704
Toronto (Ontario) Canada M9A 0B4
P 416 899-0073 F 844 891-2549
Phytronix Technologies
Québec Area (Québec Metro High Tech Park)
4535, bld Wilfrid-Hamel, suite 120
Québec (Québec) Canada G1P 2J7
P 418 692-1414 F 418 692-4940
Toll free: 1 877 792-6207 Follow us @Phytronix linkedin.com/companies/phytronix
phytronix.com
