1) tiamo is Metrohm's new control and database software for titration systems and laboratory automation. It allows for titration, dosing, and complete automation of analytical workflows.
2) tiamo offers a modern user interface, powerful report generation, flexible method editor, real-time parallel titrations, client-server database, and export of data to LIMS systems.
3) As tiamo can integrate existing Titrino and new Titrando systems, it protects customers' investments while offering compatibility across different Metrohm instruments.
The document provides an overview of the 888 Titrando and 890 Titrando potentiometric titration systems from Metrohm. It summarizes their key features, which include a touch control interface, intelligent dosing units and exchange units, support for automation via sample changers, and compliance with GLP/GMP standards. The systems enable potentiometric and Karl Fischer titration using intelligent electrodes and software for method development and data management.
The Titrando is an intelligent Karl Fischer titrator that provides high-level automation and data management capabilities. It offers favorites for quick method starts, intelligent dosing elements, iConnect for mobile measuring input, and compliance with GMP/GLP and FDA regulations. The Titrando integrates with tiamo control and database software to enable complete laboratory automation through parallel titration and sample changer control.
The drug or drug combination may not be official in any pharmacopoeias.
A proper analytical procedure for the drug may not be available in the literature due to patent regulations.
Analytical methods may not be available for the drug in the form of a formulation due to the interference caused by the formulation excipients.
Analytical methods for the quantitation of the drug in biological fluids may not be available.
Analytical methods for a drug in combination with other drugs may not be available.
The existing analytical procedures may require expensive reagents and solvents. It may also involve cumbersome extraction and separation procedures and these may not be reliable.
Calibration and validation of HPLC methods involves establishing that the instrument produces accurate and reproducible results. Key aspects include:
1. Calibration involves checking parameters like flow rate accuracy, wavelength accuracy, and detector linearity using reference standards.
2. Validation establishes method performance meets requirements. It involves determining accuracy over 3 concentration levels, precision through repeatability studies, and linearity through correlation coefficients.
3. Qualification includes design, installation, operational, and performance qualification to prove equipment works correctly and leads to expected results.
This document discusses headspace analysis, which analyzes the gas above a sample in a chromatography vial. Headspace analysis is suited for very volatile analytes in solid or liquid samples, such as residual solvents in pharmaceuticals, flavors in beverages, and alcohol in blood or urine. It has advantages like minimal sample preparation and easy automation. Key factors that affect headspace analysis efficiency are the partition coefficient (K value) and phase ratio (b value), both of which can be optimized based on temperature, salts added, sample volume, and vial design. A typical headspace analyzer automatically analyzes up to 10 vials using a motorized needle and can be connected to a GC instrument. Headspace analysis is commonly used
The document discusses Karl Fischer titration (KFT) techniques for determining water content. It describes two common methods - volumetric KFT, which uses a burette to dispense Karl Fischer reagent, and coulometric titration, which generates iodine electrochemically. The key reaction involves iodine oxidizing an intermediate alkylsulfite to alkylsulfate, consuming water. Factors like solvent choice, water content, pH, and kinetics are discussed. The document also outlines how volumetric and coulometric titrators function and how the endpoint is detected.
analytical method validation and validation of hplcvenkatesh thota
The document summarizes a seminar on analytical method validation and validation of HPLC. It discusses parameters for method validation according to USP, BP, and ICH guidelines such as accuracy, precision, linearity, range, specificity, detection limit, and quantitation limit. It also covers validation of typical HPLC systems through qualification, design, installation, operational, and performance qualification. Key parameters evaluated during HPLC method validation are discussed, including system suitability tests involving retention factor, relative retention, theoretical plates, resolution, and tailing factor.
The document provides an overview of the ICH Q3C guideline for residual solvents. It classifies residual solvents into 3 classes based on risk: Class 1 solvents to be avoided, Class 2 solvents to be limited, and Class 3 solvents with low toxic potential. Limits are defined for each class, with Class 1 solvent limits being the strictest. Options for describing limits of Class 2 solvents include assuming a daily dose of 10g or adding amounts in components. Analytical procedures and reporting levels are also outlined. The goal is to recommend safe levels of residual solvents to protect patient safety.
The document provides an overview of the 888 Titrando and 890 Titrando potentiometric titration systems from Metrohm. It summarizes their key features, which include a touch control interface, intelligent dosing units and exchange units, support for automation via sample changers, and compliance with GLP/GMP standards. The systems enable potentiometric and Karl Fischer titration using intelligent electrodes and software for method development and data management.
The Titrando is an intelligent Karl Fischer titrator that provides high-level automation and data management capabilities. It offers favorites for quick method starts, intelligent dosing elements, iConnect for mobile measuring input, and compliance with GMP/GLP and FDA regulations. The Titrando integrates with tiamo control and database software to enable complete laboratory automation through parallel titration and sample changer control.
The drug or drug combination may not be official in any pharmacopoeias.
A proper analytical procedure for the drug may not be available in the literature due to patent regulations.
Analytical methods may not be available for the drug in the form of a formulation due to the interference caused by the formulation excipients.
Analytical methods for the quantitation of the drug in biological fluids may not be available.
Analytical methods for a drug in combination with other drugs may not be available.
The existing analytical procedures may require expensive reagents and solvents. It may also involve cumbersome extraction and separation procedures and these may not be reliable.
Calibration and validation of HPLC methods involves establishing that the instrument produces accurate and reproducible results. Key aspects include:
1. Calibration involves checking parameters like flow rate accuracy, wavelength accuracy, and detector linearity using reference standards.
2. Validation establishes method performance meets requirements. It involves determining accuracy over 3 concentration levels, precision through repeatability studies, and linearity through correlation coefficients.
3. Qualification includes design, installation, operational, and performance qualification to prove equipment works correctly and leads to expected results.
This document discusses headspace analysis, which analyzes the gas above a sample in a chromatography vial. Headspace analysis is suited for very volatile analytes in solid or liquid samples, such as residual solvents in pharmaceuticals, flavors in beverages, and alcohol in blood or urine. It has advantages like minimal sample preparation and easy automation. Key factors that affect headspace analysis efficiency are the partition coefficient (K value) and phase ratio (b value), both of which can be optimized based on temperature, salts added, sample volume, and vial design. A typical headspace analyzer automatically analyzes up to 10 vials using a motorized needle and can be connected to a GC instrument. Headspace analysis is commonly used
The document discusses Karl Fischer titration (KFT) techniques for determining water content. It describes two common methods - volumetric KFT, which uses a burette to dispense Karl Fischer reagent, and coulometric titration, which generates iodine electrochemically. The key reaction involves iodine oxidizing an intermediate alkylsulfite to alkylsulfate, consuming water. Factors like solvent choice, water content, pH, and kinetics are discussed. The document also outlines how volumetric and coulometric titrators function and how the endpoint is detected.
analytical method validation and validation of hplcvenkatesh thota
The document summarizes a seminar on analytical method validation and validation of HPLC. It discusses parameters for method validation according to USP, BP, and ICH guidelines such as accuracy, precision, linearity, range, specificity, detection limit, and quantitation limit. It also covers validation of typical HPLC systems through qualification, design, installation, operational, and performance qualification. Key parameters evaluated during HPLC method validation are discussed, including system suitability tests involving retention factor, relative retention, theoretical plates, resolution, and tailing factor.
The document provides an overview of the ICH Q3C guideline for residual solvents. It classifies residual solvents into 3 classes based on risk: Class 1 solvents to be avoided, Class 2 solvents to be limited, and Class 3 solvents with low toxic potential. Limits are defined for each class, with Class 1 solvent limits being the strictest. Options for describing limits of Class 2 solvents include assuming a daily dose of 10g or adding amounts in components. Analytical procedures and reporting levels are also outlined. The goal is to recommend safe levels of residual solvents to protect patient safety.
1. Atomic absorption spectroscopy is an analytical technique used to determine the concentration of elemental impurities in samples. It works by measuring the amount of light absorbed by atomic vapor of an element at a specific wavelength.
2. There are different components used for atomic absorption spectroscopy including a flame, graphite furnace, or hydride system for atomization. Sample preparation and instrument optimization are also important steps.
3. Common elements that can be analyzed include sodium, lithium, and potassium using a flame atomization system. Graphite furnace spectroscopy and hydride generation are also introduced for improved sensitivity. Background correction methods are discussed to improve accuracy.
This document provides an overview of HPLC methodology and validation requirements. It discusses the key components of an HPLC test procedure including system suitability testing, relative response factors, and the validation parameters of specificity, linearity, accuracy, precision, LOD/LOQ, and robustness. Validation requirements depend on whether the method is compendial or non-compendial, with full validation needed for non-compendial methods. System suitability criteria and validation acceptance limits are outlined for various analytical techniques like assay, impurities testing, and dissolution.
IMPURITY PROFILING (SOURCES OF IMPURITIES)N Anusha
The description, characterization and quantitation of identified and unidentified impurities present in the drug substances is known as impurity profile.
IMPURITIES in pharmaceuticals are unwanted chemicals, that even in small amounts may influence the efficacy and safety of the pharmaceutical products.
This document provides an overview of high-performance liquid chromatography (HPLC). It describes HPLC as a chromatographic technique used to separate components of a mixture for identifying, quantifying, or purifying individual components. The document outlines the history, instrumentation, operation, types, advantages, and disadvantages of HPLC. It explains that HPLC involves a mobile phase, column, pump, injector, detector, and computer to separate sample components based on their interactions with the stationary phase.
Validation of pharaceutical water system and pure steamJp Prakash
This document discusses the validation of pharmaceutical water systems and pure steam. It covers the validation sequences of design qualification, installation qualification, operational qualification, and performance qualification. Design qualification involves validating components like piping, tanks, filters, and distillation stills. Installation qualification ensures proper installation. Performance qualification demonstrates the system can reliably produce water and steam meeting quality requirements over extended use. Validation is necessary to assure safety, efficacy and quality according to regulations.
To recommend acceptable amounts for residual solvents in pharmaceuticals for the safety of the patient. The guideline recommends use of less toxic solvents and describes levels considered to be toxicologically acceptable for some residual solvents.
The guideline applies to all dosage forms and routes of administration.
This guidelines does not address all possible solvents, only those identified in drugs at that time, neither address solvents intentionally used as excipients nor solvates.
The maximum acceptable intake per day of residual solvent in pharmaceutical products is defined as “permitted daily exposure” (PDE)
Previously, another terms were used like “Tolerable daily intake” (TDI) & “Acceptable daily intake” (ADI) by different organization & authorities, but now usually this new term “PDE” is used
The document discusses column efficiency in chromatography. It introduces the van Deemter equation, which describes the factors that influence column efficiency through the plate height (H). The factors are eddy diffusion (A term), longitudinal diffusion (B term), and resistance to mass transfer (C term). Smaller particle size, better packing, and optimal flow rate can improve efficiency by minimizing the terms in the van Deemter equation. The C term, in particular, increases with flow rate, so there is an optimal flow where efficiency is highest.
Performance qualification of High performance liquid chromatography Atchaya Thalapathy
This document discusses performance qualification (PQ) of high performance liquid chromatography (HPLC). PQ is part of the instrument qualification process and demonstrates that the HPLC system consistently performs according to specifications. The document outlines several PQ tests for the HPLC including injector precision and linearity, resolution between peaks, solvent delivery flow rate accuracy and precision, and detector parameters. It provides details on how to conduct these tests and acceptance criteria to ensure the HPLC is functioning properly.
A Review on Step-by-Step Analytical Method Validationiosrphr_editor
When analytical method is utilized to generate results about the characteristics of drug related samples it is essential that the results are trustworthy. They may be utilized as the basis for decisions relating to administering the drug to patients. Analytical method validation required during drug development and manufacturing and these analytical methods are fit for their intended purpose. To comply with the requirements of GMP pharmaceutical industries should have an overall validation policy which documents how validation will be performed. The purpose of this validation is to show that processes involved in the development and manufacture of drug, production and analytical testing can be performed in an effective and reproducible manner. This review article provides guidance on how to perform validation characteristics for the analytical method which are utilized in pharmaceutical analysis.
Analysis of fermentation products of (2) (1)prakash64742
The document provides information on the analysis of fermentation products of spirits. It discusses the key constituents typically found in spirits like brandy, gin, rum, whisky and vodka. These include alcohols, acids, esters, aldehydes and others. The document also describes analytical tests prescribed for analyzing spirits, such as tests for alcohol content, total solids, acidity, esters and others. Distillation is used to produce spirits from fermented liquors resulting in products high in alcohol that do not spoil microbially.
Nano liquid chromatography uses columns with internal diameters between 20-100 μm and flow rates of nanoliters per minute, providing advantages over traditional HPLC including lower mobile phase and sample consumption, high separation efficiency even with small samples, and easy coupling to mass spectrometry. The document discusses how nano LC is well-suited for pharmaceutical analysis applications requiring detection of drugs and pharmaceuticals at nano or low levels.
University Institute of Pharmaceutical Sciences is a flag bearer of excellence in Pharmaceutical education and research in the country. Here is another initiative to make study material available to everyone worldwide. Based on the new PCI guidelines and syllabus here we have a presentation dealing with qualifications of HPLC which is the " High Performance Liquid Chromatography".
Thank you for reading.
Hope it was of help to you.
UIPS,PU team
The document provides information on charged aerosol detection (CAD) technology. It discusses the evolution of CAD products, how CAD works, comparisons to other detection methods like ELSD, and example applications. Key points covered include how CAD provides a uniform response for analytes independent of chemical structure, its wide dynamic range of up to four orders of magnitude, and how it can detect both non-volatile and semi-volatile compounds on HPLC and UHPLC systems without the need for reference standards.
The document outlines common problems encountered during HPLC troubleshooting and provides potential causes and solutions for each. It discusses five major categories of symptoms: pressure abnormalities, leaks, chromatogram issues, injector problems, and other issues detected by smell, sight or sound. Correcting any problems should be recorded in the system record book to aid in resolving future issues.
The document discusses the development and validation of an LC-MS/MS bioanalytical method for the determination of a drug in human plasma. It describes the objectives, which are to develop a specific, reliable and cost-effective method. It outlines the key steps in method development including literature search, reference standard preparation, extraction procedure selection, and optimization of separation and detection. The validation parameters that will be evaluated are also summarized, including specificity, accuracy, precision, recovery, matrix effects and stability.
qualification of analytical instruments..M pharmacy 1st year.validationSohailPattan
The document discusses the qualification and calibration of analytical instruments like electronic balances and UV-Visible spectrophotometers. It provides details on the various tests and parameters to be checked during qualification of these instruments to ensure they meet performance requirements. These include tests for baseline flatness, wavelength accuracy, transmittance, absorbance, emission lines, stray light, resolution and photometric linearity. The document also outlines the recommended frequency of qualification and calibration.
Handling of Refernce Standards_Dr.A.Amsavel Dr. Amsavel A
Definition
Requirements
Guidelines
Pharmacopiea
Types of Reference Standards
SOP for handling of Reference Standards
Qualification of Secondary Standards
Assigning Potency, Storage and Use
Documents & Records
Reduce The Risk Critical To Protect Critical To Monitorjellobrand
The document discusses how IBM Tivoli Monitoring (ITM) can provide system performance and state monitoring of servers, applications, and infrastructure to complement Tivoli Storage Manager (TSM) backup and recovery. ITM monitors resources like CPU, memory, and network performance and detects issues before they cause outages. It offers out-of-the-box reporting, monitoring, situations, and automated responses to improve problem resolution. When used together, ITM and TSM provide a comprehensive solution for data protection, backup monitoring, and overall system health.
Your data is in Prometheus, now what? (CurrencyFair Engineering Meetup, 2016)Brian Brazil
Prometheus is a next-generation monitoring system with a time series database at it's core. Once you have a time series database, what do you do with it though? This talk will look at getting data in, and more importantly how to use the data you collect productively.
Contact us at prometheus@robustperception.io
1. Atomic absorption spectroscopy is an analytical technique used to determine the concentration of elemental impurities in samples. It works by measuring the amount of light absorbed by atomic vapor of an element at a specific wavelength.
2. There are different components used for atomic absorption spectroscopy including a flame, graphite furnace, or hydride system for atomization. Sample preparation and instrument optimization are also important steps.
3. Common elements that can be analyzed include sodium, lithium, and potassium using a flame atomization system. Graphite furnace spectroscopy and hydride generation are also introduced for improved sensitivity. Background correction methods are discussed to improve accuracy.
This document provides an overview of HPLC methodology and validation requirements. It discusses the key components of an HPLC test procedure including system suitability testing, relative response factors, and the validation parameters of specificity, linearity, accuracy, precision, LOD/LOQ, and robustness. Validation requirements depend on whether the method is compendial or non-compendial, with full validation needed for non-compendial methods. System suitability criteria and validation acceptance limits are outlined for various analytical techniques like assay, impurities testing, and dissolution.
IMPURITY PROFILING (SOURCES OF IMPURITIES)N Anusha
The description, characterization and quantitation of identified and unidentified impurities present in the drug substances is known as impurity profile.
IMPURITIES in pharmaceuticals are unwanted chemicals, that even in small amounts may influence the efficacy and safety of the pharmaceutical products.
This document provides an overview of high-performance liquid chromatography (HPLC). It describes HPLC as a chromatographic technique used to separate components of a mixture for identifying, quantifying, or purifying individual components. The document outlines the history, instrumentation, operation, types, advantages, and disadvantages of HPLC. It explains that HPLC involves a mobile phase, column, pump, injector, detector, and computer to separate sample components based on their interactions with the stationary phase.
Validation of pharaceutical water system and pure steamJp Prakash
This document discusses the validation of pharmaceutical water systems and pure steam. It covers the validation sequences of design qualification, installation qualification, operational qualification, and performance qualification. Design qualification involves validating components like piping, tanks, filters, and distillation stills. Installation qualification ensures proper installation. Performance qualification demonstrates the system can reliably produce water and steam meeting quality requirements over extended use. Validation is necessary to assure safety, efficacy and quality according to regulations.
To recommend acceptable amounts for residual solvents in pharmaceuticals for the safety of the patient. The guideline recommends use of less toxic solvents and describes levels considered to be toxicologically acceptable for some residual solvents.
The guideline applies to all dosage forms and routes of administration.
This guidelines does not address all possible solvents, only those identified in drugs at that time, neither address solvents intentionally used as excipients nor solvates.
The maximum acceptable intake per day of residual solvent in pharmaceutical products is defined as “permitted daily exposure” (PDE)
Previously, another terms were used like “Tolerable daily intake” (TDI) & “Acceptable daily intake” (ADI) by different organization & authorities, but now usually this new term “PDE” is used
The document discusses column efficiency in chromatography. It introduces the van Deemter equation, which describes the factors that influence column efficiency through the plate height (H). The factors are eddy diffusion (A term), longitudinal diffusion (B term), and resistance to mass transfer (C term). Smaller particle size, better packing, and optimal flow rate can improve efficiency by minimizing the terms in the van Deemter equation. The C term, in particular, increases with flow rate, so there is an optimal flow where efficiency is highest.
Performance qualification of High performance liquid chromatography Atchaya Thalapathy
This document discusses performance qualification (PQ) of high performance liquid chromatography (HPLC). PQ is part of the instrument qualification process and demonstrates that the HPLC system consistently performs according to specifications. The document outlines several PQ tests for the HPLC including injector precision and linearity, resolution between peaks, solvent delivery flow rate accuracy and precision, and detector parameters. It provides details on how to conduct these tests and acceptance criteria to ensure the HPLC is functioning properly.
A Review on Step-by-Step Analytical Method Validationiosrphr_editor
When analytical method is utilized to generate results about the characteristics of drug related samples it is essential that the results are trustworthy. They may be utilized as the basis for decisions relating to administering the drug to patients. Analytical method validation required during drug development and manufacturing and these analytical methods are fit for their intended purpose. To comply with the requirements of GMP pharmaceutical industries should have an overall validation policy which documents how validation will be performed. The purpose of this validation is to show that processes involved in the development and manufacture of drug, production and analytical testing can be performed in an effective and reproducible manner. This review article provides guidance on how to perform validation characteristics for the analytical method which are utilized in pharmaceutical analysis.
Analysis of fermentation products of (2) (1)prakash64742
The document provides information on the analysis of fermentation products of spirits. It discusses the key constituents typically found in spirits like brandy, gin, rum, whisky and vodka. These include alcohols, acids, esters, aldehydes and others. The document also describes analytical tests prescribed for analyzing spirits, such as tests for alcohol content, total solids, acidity, esters and others. Distillation is used to produce spirits from fermented liquors resulting in products high in alcohol that do not spoil microbially.
Nano liquid chromatography uses columns with internal diameters between 20-100 μm and flow rates of nanoliters per minute, providing advantages over traditional HPLC including lower mobile phase and sample consumption, high separation efficiency even with small samples, and easy coupling to mass spectrometry. The document discusses how nano LC is well-suited for pharmaceutical analysis applications requiring detection of drugs and pharmaceuticals at nano or low levels.
University Institute of Pharmaceutical Sciences is a flag bearer of excellence in Pharmaceutical education and research in the country. Here is another initiative to make study material available to everyone worldwide. Based on the new PCI guidelines and syllabus here we have a presentation dealing with qualifications of HPLC which is the " High Performance Liquid Chromatography".
Thank you for reading.
Hope it was of help to you.
UIPS,PU team
The document provides information on charged aerosol detection (CAD) technology. It discusses the evolution of CAD products, how CAD works, comparisons to other detection methods like ELSD, and example applications. Key points covered include how CAD provides a uniform response for analytes independent of chemical structure, its wide dynamic range of up to four orders of magnitude, and how it can detect both non-volatile and semi-volatile compounds on HPLC and UHPLC systems without the need for reference standards.
The document outlines common problems encountered during HPLC troubleshooting and provides potential causes and solutions for each. It discusses five major categories of symptoms: pressure abnormalities, leaks, chromatogram issues, injector problems, and other issues detected by smell, sight or sound. Correcting any problems should be recorded in the system record book to aid in resolving future issues.
The document discusses the development and validation of an LC-MS/MS bioanalytical method for the determination of a drug in human plasma. It describes the objectives, which are to develop a specific, reliable and cost-effective method. It outlines the key steps in method development including literature search, reference standard preparation, extraction procedure selection, and optimization of separation and detection. The validation parameters that will be evaluated are also summarized, including specificity, accuracy, precision, recovery, matrix effects and stability.
qualification of analytical instruments..M pharmacy 1st year.validationSohailPattan
The document discusses the qualification and calibration of analytical instruments like electronic balances and UV-Visible spectrophotometers. It provides details on the various tests and parameters to be checked during qualification of these instruments to ensure they meet performance requirements. These include tests for baseline flatness, wavelength accuracy, transmittance, absorbance, emission lines, stray light, resolution and photometric linearity. The document also outlines the recommended frequency of qualification and calibration.
Handling of Refernce Standards_Dr.A.Amsavel Dr. Amsavel A
Definition
Requirements
Guidelines
Pharmacopiea
Types of Reference Standards
SOP for handling of Reference Standards
Qualification of Secondary Standards
Assigning Potency, Storage and Use
Documents & Records
Reduce The Risk Critical To Protect Critical To Monitorjellobrand
The document discusses how IBM Tivoli Monitoring (ITM) can provide system performance and state monitoring of servers, applications, and infrastructure to complement Tivoli Storage Manager (TSM) backup and recovery. ITM monitors resources like CPU, memory, and network performance and detects issues before they cause outages. It offers out-of-the-box reporting, monitoring, situations, and automated responses to improve problem resolution. When used together, ITM and TSM provide a comprehensive solution for data protection, backup monitoring, and overall system health.
Your data is in Prometheus, now what? (CurrencyFair Engineering Meetup, 2016)Brian Brazil
Prometheus is a next-generation monitoring system with a time series database at it's core. Once you have a time series database, what do you do with it though? This talk will look at getting data in, and more importantly how to use the data you collect productively.
Contact us at prometheus@robustperception.io
When first designing industrial automation projects, it’s easy to make some common mistakes that can make integrating harder than it needs to be and cause headaches down the road. The best way to set yourself up for success is to recognize best practices as soon as possible. Not only does this save time on rework and future development, but it also allows for more predictability, better organization, and increased functionality.
Powering Real-Time Decisions with Continuous Data StreamsSafe Software
In an era where making swift, data-driven decisions can set industry leaders apart, understanding the world of data streaming and stream processing is crucial. During this webinar, we'll explore:
Stream Processing Overview: Dive into what stream processing entails and the value it brings organizations.
Stream vs. Batch Processing: Learn the key differences and benefits of stream processing compared to traditional batch processing, highlighting the efficiency of real-time data handling.
Mastering Data Volumes: Discover strategies for effectively managing both high and low volume data streams, ensuring optimal performance.
Boosting Operational Excellence: Explore how adopting data streaming can enhance your organization's operational workflows and productivity.
Spatial Data's Role in Streams: Understand the importance of spatial data in stream processing for more informed decision-making.
Interactive Demos: Watch practical demos, from dynamic geofencing to group-based processing.
Plus, we’ll show you how you can do it without coding! Register now to take the first step towards more informed, timely, and precise decision-making for your organization.
Microtorque Tightening - Smart Tools for the Smart FactoryCeciliaHamrn
Realizing the Smart Factory with Atlas Copco MicroTorque
Industry 4.0 – The Fourth Industrial Revolution – is driving the evolution of the assembly process. The digitalization
of manufacturing and assembly means shifting the way we look at manufacturing in terms of production optimization and
automation.
The more informed you are, the better decisions you can make. Having smart tools on your line means that you have
specific tightening information fed into the production system, information communicated to you concerning critical
details of your components, materials and tightening process. This provides a valuable opportunity to increase efficiency and
results with pro-active problem solving,alongside with considerable energy savings from efficiency improvements.
We call it – Smart Connected Assembly.
Tally.ERP 9 is a business management software that allows users to manage accounting, finance, point of sale, payroll, and branch management from a centralized application. It has features such as simplicity, speed, power, flexibility, scalability, multi-lingual capability, and real-time processing. Tally.ERP 9 also offers technical support, online help, remote access, and an auditors' edition. Users can create companies, make accounting entries, generate reports, and customize settings through its user-friendly interface.
1) Trilogy's managed IT service promises to automate essential recurring IT tasks, identify problems before they occur, and provide greater control and visibility over a company's technology platform.
2) This will save companies a minimum of 25% on their IT costs while freeing up IT teams to focus on business applications that drive performance instead of routine infrastructure tasks.
3) Trilogy claims their service offers real-time visibility into a company's entire IT infrastructure with powerful reporting capabilities through customized scripts tailored for each business.
KantanMT is a cloud-based machine translation platform that reduces translation costs and speeds up the translation process using customization features. It supports over 760 language pairs and guarantees client data confidentiality. Users can build customized translation engines by uploading training data like translation memories and monolingual files, then translate documents with the click of a button.
Enterprise Storage Solutions for Overcoming Big Data and Analytics ChallengesINFINIDAT
Big Data and analytics workloads represent a new frontier for organizations. Data is being collected from sources that did not exist 10 years ago. Mobile phone data, machine-generated data, and website interaction data are all being collected and analyzed. In addition, as IT budgets are already being pressured down, Big Data footprints are getting larger and posing a huge storage challenge.
This paper provides information on the issues that Big Data applications pose for storage systems and how choosing the correct storage infrastructure can streamline and consolidate Big Data and analytics applications without breaking the bank.
InfiniBox bridges the gap between high performance and high capacity for Big Data applications. InfiniBox allows an organization implementing Big Data and Analytics projects to truly attain its business goals: cost reduction, continual and deep capacity scaling, and simple and effective management — and without any compromises in performance or reliability. All of this to effectively and efficiently support Big Data applications at a disruptive price point.
Learn more at www.infinidat.com.
Microservices and Prometheus (Microservices NYC 2016)Brian Brazil
Brian Brazil is an engineer passionate about reliable systems. He has experience at Google SRE and Boxever. He is the founder of Robust Perception and a contributor to open source projects including Prometheus. Prometheus is a monitoring system designed for microservices that allows inclusive, scalable monitoring across languages and services. It uses labels, queries, and federation to provide powerful yet manageable monitoring of dynamic environments.
Thango : Extrusion cost savings - public presentationThango
Discover the features of Thango(C): the new SW-HW integrated system that allows consistent cost savings in the die correction and die seign process management! Let's Thango together! Start saving now by joining our team of International Thango users.
www.aluthango.com, thango@aluthango.com
It is no longer efficient, nor even possible, to properly manage your infrastructure with manual processes performed in an ad hoc, incident-based manner. You must be able to continuously monitor, assess, adjust and restructure every part of your multiplatform, distributed, interconnected and internet-dependent cyber-multiverse to respond to constantly changing business requirements.
Elevate Capacity Management (formerly Athene) provides leading companies with the cross-platform capacity management solution they need to meet their capacity management challenges. The new release of Elevate Capacity Management adds new features to ensure data integrity, improve data filtering, and provide more flexibility in customizing the most important thresholds in your IT environment.
View this webinar on-demand and learn about these new features including:
• Performance enhancement for large scale data ingestion and reporting
• The ability to use virtually any metric as a threshold for monitoring and alerting
• A faster and more scalable multi-threaded data management architecture
Prometheus is a next-generation monitoring system. It lets you see you not just what your systems look like from the outside, but also gives visibility into the internals and business aspects of your systems. This allows everyone to benefit, including both operations and developers. This talk will look at the concepts behind monitoring with Prometheus, how it's designed, why it's suitable for Cloud Native environments and how you can get involved.
An overview of the different sets of functionality of Tableau solution suite, and how it can address the many facets of a comprehensive data mining solution.
How to Improve Data Labels and Feedback Loops Through High-Frequency Sensor A...InfluxData
Ezako is a startup specializing in time series analysis. Ezako helps its clients detect anomalies and label their time series data. It helps accelerate the labeling process and analyze vast amounts of data from a variety of sensors in real-time. The company provides anomaly insights and makes it easier for data scientists. Ezako is the creator of Upalgo, which is a time series data management tool that uses AI to automatically detect anomalies in streaming data.
During this webinar, Ezako will dive into how high-frequency sensors can generate huge amounts of data which can become desynchronized. This can result in data quality issues as it can contain errors and glitches. Ezako uses machine learning, labelling and feedback loops to identify these errors. Discover how the company helps improve its clients’ data quality and reduce the number of validation mistakes.
The document discusses ancoraDocs Invoices, an invoice processing software system. It can process thousands of invoices per year for companies of various sizes in an automated way. The system speeds up invoice data entry, improves data accuracy, and helps gain better control over cash flow. It can be customized for other applications beyond invoice processing like purchase orders or HR documents.
Advantages And Disadvantages Of Cyber-Crime In The HotelPatty Buckley
This document discusses cybercrime and transaction processing systems in hotels. It defines cybercrime and lists some types that could affect hotels, such as hacking reservations or stealing credit card numbers. It also defines a transaction processing system (TPS) as a system that processes transactions, gives examples of what it could be used for in a hotel like payroll and purchases, and lists advantages like cost effectiveness and increased efficiency and disadvantages like costs and need for maintenance. It recommends a hotel implement a TPS to help with transactions.
Manual titration can be automated with ECO TITRATOR - save time and increase ...Metrohm India Limited
The Eco Titrator is a compact, automatic titration device that can save up to 120 titration methods. It performs titrations simply and reliably with a touch interface. It offers precise dosing, GLP-compliant documentation, and can be used for a variety of applications across industries like food and beverages, water analysis, petrochemistry, and more. Local sales organizations provide support worldwide.
Global webinar on Advanced solutions for battery material characterizationMetrohm India Limited
Webinar highlights:
-Introduction into the working principle of li-ion batteries and solid-state batteries
-Combined precision and automation: The Microcell HC setup and Metrohm Autolab devices
-The basic principle: quick and precise adjustment of the sample’s temperature by Peltier-technique
-One modular setup for different battery-related applications: determination of the conductivity of liquid and solid electrolytes, the MacMullin number of electrolyte-soaked separator foils, and the electrochemical properties of interfaces
Do you have that spark to move the world with your innovative research? Presenting IIT Bombay Metrohm Young Chemist Award 2019 – a perfect stage for all the researchers in Chemistry domain to showcase their work. Innovation in research is the essence of this contest and we recognise & award the brilliance that completes this criteria in all realms.
Application note on purified water for mammalian and bacterial cell cultureMetrohm India Limited
To achieve success in mammalian cell culture it is necessary to use extremely pure media and buffers. The use of Type I ultrapure water
to effectively eliminate the presence of biologically active species and other contaminants which could interfere with the culturing
process is essential. General laboratory grade purified water (Type II) with low levels of bacterial and organic contamination is usually
sufficiently pure for bacterial cell culture.
This document discusses quality control and analysis in power plants, focusing on three key areas:
1. Process water analysis, including parameters like pH, conductivity, hardness, and impurities. Continuous monitoring is important for processes and water chemistry.
2. Turbine oil and lubricant analysis to check properties like acid/base numbers and water content per industry standards.
3. Fuel and operating material analysis using ion chromatography to determine halogens and sulfur in samples like coal.
The document provides an overview of analytical techniques and standards for monitoring various circuits and materials in power plants to ensure safe, efficient, and reliable operations. Metrohm offers solutions for many of the described applications and parameters.
The 875 KF Gas Analyzer provides a robust solution for determining trace amounts of water in gases using automated coulometric Karl Fischer titration. It excels through its durable design and can analyze both liquid and permanent gases. The system consists of a control unit and analysis module equipped to handle gases and perform the water analysis cell fully automatically. It is ideal for routine water analysis in laboratories and industries such as refrigerants and natural gas.
Ti-Touch is a new device that aims to simplify titration experiments. It uses touchscreen technology to allow users to easily perform titrations on a mobile platform. This new device could make titration experiments more accessible and reduce errors by automating much of the process.
The document describes two new pH meters from Metrohm: the 780 pH Meter and the 781 pH/Ion Meter. Both meters offer high quality, easy operation, and advanced features. The 781 meter allows for both pH and ion concentration measurements using ion-selective electrodes. Both meters provide calibration functions, electrode testing, data storage, and quality control monitoring. The document compares the key specifications and capabilities of the two meters.
The 756 KF Coulometer provides automated coulometric Karl Fischer titration for determining low water contents down to the microgram range. It features a backlit LCD screen, integrated printer, methods memory, and interfaces for connecting additional devices. The instrument guarantees accurate and reproducible results for applications such as solvents, industrial products, finished products, and solids using appropriate sample introduction methods and optional accessories like the 768 KF Drying Oven.
Metrohm – customized analysis for surface finishing, Process control in elect...Metrohm India Limited
Metrohm offers analytical solutions for quality control of basic chemicals and raw materials used in surface finishing processes. Titration can be used to determine concentrations of common acids and bases. Ion chromatography can detect impurities in chemicals like hydrogen peroxide and isopropanol by using inline matrix elimination. When ultratraces need to be found, inline preconcentration can be added for high sensitivity analysis.
Metrohm offers analytical solutions for quality control of basic chemicals and raw materials used in surface finishing processes. Titration can be used to determine concentrations of common acids and bases. Ion chromatography can detect impurities in chemicals like hydrogen peroxide and isopropanol by using inline matrix elimination. When ultratraces need to be found, inline preconcentration can be added for high sensitivity analysis.
The document describes two pH meters, the 780 pH Meter and 781 pH/Ion Meter, produced by Metrohm. Both devices combine high quality with advanced design and offer numerous measurement and calibration functions. The 781 meter allows for additional ion concentration measurements using ion-selective electrodes. Both meters feature easy operation, automated quality control functions, and compatibility with Metrohm accessories for enhanced measurement capabilities.
This document discusses analytical instrumentation for battery research. It summarizes several techniques for characterizing batteries including: electrochemical characterization to determine current/voltage characteristics and test charging; determination of water content which must be very low; and determination of anions and cations by ion chromatography to analyze electrolyte composition. Sophisticated instrumentation is needed for production and analysis of battery materials and cells to advance progress in battery research.
We offer you state-of-the-art instrumentation helping you to check and improve the quality of biofuels and corresponding blends as well as to comply with the standards – in your laboratory but also atline and online in the process environment
The document describes various accessories available from Metrohm for analytical instrumentation such as sample changers, thermal sample preparation devices, dosing units, filtration equipment, software, additional stations, eluent and calibration techniques, and kits for voltammetry and mercury/arsenic analysis to enhance automation and efficiency. The accessories aid in sample handling, separation, data management, and analysis across various applications like Karl Fischer titration, ion chromatography, and voltammetry. Contact information is provided for Metrohm India Limited and their local distributor.
Metrohm has taken ion chromatography to an entirely new level. We are proud to offer you the Professional IC product family – the first ion chromatography systems made up of intelligent components for:
- Anions and cations in drinking water
- Ultratrace analysis
- Ions in complex sample matrices
- Method development in R & D
Your key benefits with Metrohm ion chromatography:
* High sensitivity right down to the ppt level
* Accurate and reproducible results
* Ease of use due to
intelligent IC components
* monitoring and controlling functions
*Metrohm Inline Sample Preparation (MISP)
* Low cost of ownership
* Reliable and affordable service and support
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
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Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
3. • tiamo points the way 4/5
• tiamo at a glance 6
• tiamo makes work a pleasure 7
• tiamo brings you more... 8/9
• ... and more... 10/11
• ... and even more 12/13
• Future-proof thanks to client-server option 14/15
• Unlimited flexibility 16/17
• Further innovative features of tiamo 18/19
• Prepared for the audit 20/21
• Ordering information 22
• System requirements 23
3
5. tiamo – titration and more
tiamo is a control and database software for titrators and
dosing devices as well as for complete laboratory auto-
mation up to a client-server system. This is why the name
tiamo stands for «titration and more» – tiamo can do
more than just titrate. tiamo is a titration network (NTDS
= Networked Titration Data System).
tiamo is the result of Metrohm’s largest and most modern
software project. With its numerous innovations, user
friendliness and flexibility, tiamo is the leading software
package for titrations.
the way
Bringing together what belongs together
tiamo is the successor to TiNet and Workcell. Metrohm
now offers you worldwide a uniform software package
for laboratory automation. This means that, as an interna-
tionally operating company, all your subsidiaries can use a
single software platform in their laboratories for titrations.
Your benefits: data and methods can be exchanged
without any losses.
tiamo brings together the world of Titrinos and the new
Titrando system generation. In the software sector such
compatibility with existing Metrohm instruments is not just
a matter of course. The whole Titrino family, which was
previously also controlled by TiNet, can continue to be
operated under tiamo, and this after being on the market
for more than ten years! That's how Metrohm protects
your investments!
5
6. tiamo at a glance
tiamo is easy to use
• New, progressive software interface
• Freely configurable desktop thanks to new Layout Manager
• Powerful report generator
• Automatic database backup
• Graphical method editor
tiamo communicates
• Real client-server database software
• Real parallel titrations
• Data export in XML, etc.
• E-Mail function for results and messages
tiamo overcomes boundaries
• Titrando and Titrino can be used in one system
• Central user administration
• Complete traceability of all results
• Extended method commands
• Developed and validated for cGxP
6
7. tiamo makes work a pleasure
Your new workplace
The modern user interface makes it easy for
you to familiarize yourself with tiamo. All the
commands and controls are to be found where
you expect them to be.
The tiamo bar allows direct access to the four
program parts of tiamo:
• Workplace
• Database
• Methods
• Configuration
These buttons may be visible or concealed,
depending on the user’s access rights.
The information windows are in the center. In
the run window you can comfortably enter all
the sample data, whether for a single sample
or for a whole sample series.
The live display window informs you about
freely definable method instructions and shows
the live curve during the titration. The method
window provides information about the cur-
rent method status. If necessary, you have live
access to the method parameters. In the report
window you can view the current reports of
the last determinations.
7
8. tiamo brings you more...
Layout Manager – each user gets his or her own tiamo
With the novel Layout Manager the user interface can be arranged so that each user only sees
those windows that are really necessary. This saves time; cluttered-up screens are now a thing of
the past.
You can also freely define what information is to be shown in the windows.
Making four from one – parallel titrations
You can subdivide the user interface even further to create up to four independent workplaces.
In this way you can elegantly control different titration systems that are all connected to the same
PC. And all this in parallel – and, if necessary, with different users. This means that tiamo offers
maximum utilization of the analytical system.
tiamo carries out tedious routine work
Do you enter your sample data manually or do you use a barcode reader? In both cases tiamo
helps you to fill in the sample table. Continually repeated sample identifications can be saved as
text templates. tiamo also takes care of the sequential numbering. Importing the sample table?
Just let your LIMS draw up the sample table for tiamo! Avoid surprises when using a sample
changer – let tiamo check the sample table for sample weights that are too high. You can use
the sample assignment table to link sample numbers with methods. This makes your tiamo the
easiest to operate routine system in your lab!
8
10. ... and more...
Database
The database is a further trump from tiamo.
Not only your determinations, but all the
settings, methods and user information are
stored in the tiamo database and protected
against manipulation and loss.
Data Manager
Manage your data in the determination over-
view, where you can obtain the most important
information about any sample in tabular and
freely configurable form. Powerful search and
filter tools provide support. Even among thou-
sands of titrations you are sure to find your own
particular determination – in just a few seconds.
Curve window
The titration curve is shown for each
determination. The curve layout can be
freely defined. Do you want to include
the titration curve in a Word document?
No problem.
10
11. Total traceability Immediately recognize what matters
Who carried out a determination and when? Provide yourself with a quick overview in
What titrator was used? What alterations the results window. No long searching
have been made to the determination and by for the result – here you will find all the
whom? The unique traceability of the tiamo important results and calculation details
system leaves no questions unanswered. in compact form.
11
12. ... and even more
Determination reprocessing
Wrong sample weight? No problem. With the reprocessing function the sample weight can be
quickly corrected or a calculation formula adapted. Endpoint not recognized correctly? tiamo
can help here as well. You can evaluate the curve again. And you do not have to worry about
the documentation. tiamo automatically records all alterations.
History
tiamo manages all the versions of a determination. The history function provides you with the
necessary overview.
Signatures
You can provide digital signatures for the determinations. tiamo offers signatures at two levels. As
soon as a determination has a level 2 signature, the data are protected against further alterations.
Report generator
The unique report generator allows you to
arrange your analytical report layout as you
want. You can adapt one of the many report
templates to suit your particular requirements.
There is no limit to what you can do; you can
include any imaginable information in your
tiamo report.
Do you need an analysis report? Just mark the
determination in the database, select a report
template and off it goes. You can even send
your analytical reports comfortably by E-Mail!
Data export
Do you want to process your data further in
Excel or are you planning to include tiamo
in a LIMS? No problem – tiamo offers you a
wide range of export formats, including the
modern XML format. All imaginable office
applications, databases and long-term
archiving programs are available for your
data. tiamo's flexibility is unbeatable!
Control chart
tiamo can produce a control chart for your
determinations at the touch of a button.
Present your measured values in chrono-
logical order. Print them out, save them
as a pdf document or use them in Office
applications. Ready!
12
14. Future-proof thanks
to client-server option
Client-server database
In the simplest case you just install the database on your local computer. tiamo will grow together
with your requirements. As soon as data security and central data management make it necessary,
you can set up tiamo in a client-server configuration.
Install the database on a server and all measuring and office computers will act as clients. All
results are stored centrally and can be viewed and reprocessed by all client PCs. In addition, all
clients access the same pool of methods.
Data security
tiamo supports you in safeguarding your data. Activate the automatic backup function; tiamo
will then automatically make complete copies of all determinations and configurations. This means
that if the worst comes to the worst you can recover all your settings, system configurations and
determinations within a very short time.
Central control
In addition to data security, the client-server version provides you with the possibility of central
user administration. From your office you can activate new users, assign rights of access to data
and methods or implement security policies. The administration of titration systems has never
been so simple.
14
15. Example of a client-server system comprising four lab workplaces and two office PCs.
15
16. Unlimited flexibility
Method editor – clarity creates order
The block-by-block presentation of a method is clear and tidy. This makes operation child’s play.
You just make a selection from the list of method templates provided, quickly insert a calculation
template, add a report template and you can start the titration. It’s as easy as that!
Quick access to details
The detailed parameters can be accessed quickly with a double-click on the particular method
block.
You regard increased flexibility as being the key to solving your future problems?
Then tiamo is the ideal tool for you. Flexibility is one of the main advantages of this software
package. You can compile measuring commands, titrations, queries, calculations, database entries,
export instructions and sample changer commands, and this in any sequence, according to the
motto: «Nothing is impossible».
START EXIT SERIES START SERIES END
Main track Exit track Series start track Series end track
MOVE CALC CAL LOOP pH MOVE
Move to sample Calculations Calibration Cond beaker
DET pH REPORT MOVE LIFT
DET pH Report Buffer Work position
PUMP DATABASE CAL MEAS pH END
Rinse electrode Database CAL MEAS pH Series end track
END EXPORT MOVE
Main track Export Move rinse beaker
END PUMP
Exit track Rinse buffer
LIFT
Shift position
END
Series start track
16
17. Titration and more
In addition to the commands that are necessary to control the measuring, dosing, titrating and
automation devices, tiamo also lets you:
• Show messages on the screen to guide the user through a sample preparation procedure.
• Ask for the sample size and monitor result limits.
• Assign the results to different databases.
• Print out a result report and send it by E-Mail.
• Inform your colleagues automatically by E-Mail about any interference to the titration system.
• Program recurring sequences and decisions.
17
18. Further innovative features of tiamo
Configuration
All the tiamo settings are made in the configuration section.
Plug and play
Our modern USB devices ensure that all connected devices appear in the devices window.
Connect up – ready! All device data are adopted automatically.
Titrants under control
Simple organization of your titrants and solutions:
• In addition to the basic information, tiamo manages all the data required for traceability.
• tiamo even checks the working life and titer validity for you.
• If you use our uniquely intelligent dosing systems with the new «Chip on board» technology,
tiamo will prevent mix-ups.
Sensor Organizer
tiamo also manages your sensors perfectly. In this way you can ensure that all calibration intervals
are observed and only perfectly functioning electrodes are used. The calibration history of each
sensor is saved to ensure complete traceability.
Safely managed
If a computer crash should occur then your system will be quickly ready for use again if you have
automatically saved all your configuration settings. This means that «disaster recovery» poses no
problems.
18
20. Prepared for the audit
tiamo guarantees data security
Whether GMP or GLP rules, regulations on the security of electronic data (e.g. 21 CFR Part 11)
or the requirement that all results are traceable – tiamo has been developed from the very start to
meet all these requirements and therefore sets new standards.
Security has priority
Protect your data with the comprehensive security functions of tiamo. Let tiamo or Windows
monitor the passwords. Define the rules for assigning digital signatures and control access to your
data.
User administration
Add new users to the list from your office computer – tiamo assists you in doing this. Arrange the
access rights of each user in accordance with your company’s security policy. tiamo sets no limits,
but will convince you with its unique flexibility.
Complete Audit Trail
Each action performed by a tiamo user is stored automatically in the Audit Trail. This means that
you can obtain a detailed protocol about who did what and when. Data for an audit can be
prepared by pressing a button.
Version check
All data records are stored in tiamo together with their version. Protect your results against
accidental or deliberate manipulation. Use the history function to show each version of your data.
All alterations to electronic data are documented automatically – audits can no longer worry you.
Traceability
Be absolutely certain and place your confidence in the complete traceability of Metrohm software
and hardware for your titrations. Each data record contains all the raw data necessary to ensure
traceability. Unique in the world is the fact that each component used to generate the data is
documented.
20
22. Ordering information
tiamo is available in different versions and offers a suitable system for every application.
tiamo 1.0 light tiamo 1.0 full tiamo 1.0 multi
Order number 6.6056.101 6.6056.102 6.6056.103
Max. no. of devices per PC 21) Unlimited Unlimited
Supported devices See2) See2) See2)
Dialog languages English, German English, German English, German
Meets the requirements • •
of FDA 21 CFR Part 11
User administration • • •
Security policy • •
Audit Trail • •
Client-server support •
Licenses 1 1 3
Additional licenses (optional) •3)
Data export to LIMS • •
Parallel titration • •
Upgrade available •4) •5)
1) Please note that a balance or a barcode reader also counts as a connected device.
2)
Titrandos 808, 809, 835, 836, 841
Titrinos 702, 716, 718, 719, 720, 721, 736, 751, 758, 784, 785, 794, 795,
798, 799
Measuring instruments 712
KF Coulometers 756, 831
Sample changers 730, 774, 778, 789, 814, 815
Others 846, balance, barcode reader...
3) 6.6056.001 tiamo multi: 1 additional license
6.6056.002 tiamo multi: 5 additional licenses
6.6056.003 tiamo multi: 10 additional licenses
The serial no. of the tiamo multi version is required for ordering additional licenses!
4) 6.6056.106 tiamo 1.0 light upgrade to full (1 license)
6.6056.107 tiamo 1.0 light upgrade to multi (3 licenses)
5) 6.6056.108 tiamo 1.0 full upgrade to multi (3 licenses)
License policy for the client-server version
Metrohm offers you a favorable license program. tiamo multi uses runtime licenses, i.e. a license
is only required for those tiamo installations that are in use at the same time. In practice this
means that you do not need to purchase a separate license for your office computer. As a result,
when you have finished making measurements in the laboratory you can continue to use tiamo
in your office without needing a further license.
Free-of-charge updates!
You really should choose tiamo. As a Metrohm customer you will receive all future tiamo
software updates free of charge. You will also profit from new and extended tiamo functions.
22
23. System requirements
Minimum system requirements
• Processor Pentium 4; clock rate 1 GHz
• Working memory 512 MB
• Free hard disk memory 150 MB for program
• Free data memory 2 GB (for approx. 5000 determinations)
• Operating system Windows 2000 SP1, Windows XP Professional
• Connections free USB connection and/or free serial connection (RS 232C)
Additional system requirements for tiamo server
• Data line 10 MBit/s
• Operating system Windows 2000 SP1, Windows XP Professional, Windows
2000/2003 Server
23
24. I o n a n a l y s i s
Metrohm Ltd.
CH-9101 Herisau/Switzerland
Phone +41 71 353 85 85
Fax +41 71 353 89 01
www.metrohm.com
info@metrohm.com
www.titration-and-more.com
Layout Ecknauer+Schoch ASW, printed in Switzerland by Metrohm AG, Herisau
Subject to modifications
8.032.6003 – 2004-12