This document provides a quality assurance equipment measurement summary report. It details the purpose, scope, methodology, and results of measuring the accuracy and linearity of 31 LTX systems using a HP3458A standard voltage meter. Measurements from 2.5V to 5.4V on 26 sample parts were analyzed against tolerance guidelines to verify the equipment is operating within acceptable accuracy and precision limits established by standard operating procedures. Issues requiring further investigation or unacceptable results are identified. The next scheduled measurement system evaluation is also noted.
The comparison of measuring equipment against a standard instrument of higher accuracy is known as calibration. It is performed to detect, correlate, adjust, rectify and document
the accuracy of the equipment under test. Periodic calibrations are required to detect and correct the error. Periodic calibrations are an integral part of any quality system.
—Continuous Stirred Tank Reactor (CSTR) here is
considered as a nonlinear process. The CSTR is widely used in
many chemical plants. Due to changes in process parameters the
accuracy of final product can be reduced. In order to get accurate
final product the faults developed in CSTR during the chemical
reaction need to be diagnosed. If not, the faults may lead to
degrade the performance of the system. For this purpose there
are various fault diagnosis methods are to be considered. Among
the methods, the neural network predictive controller can be used
to detect faults in CSTR. Servo response is performed to
understand the behavior of CSTR. By detecting various faults
and with suitable control techniques, the accuracy of the
desirable products in CSTR can be improved
Test Strategies for Conventional Software, Unit Testing, Targets for Unit Test Cases, Common Computational Errors in Execution Paths, Other Errors to Uncover, Problems to uncover in Error Handling, Drivers and Stubs for Unit Testing, Fundamentals of Software Engineering
Software Testing Strategies, General Characteristics of Strategic Testing, Verification and Validation, Organizing for Software Testing, A Strategy for Testing Conventional Software, Levels of Testing for Conventional Software, Testing Strategy applied to Conventional Software, Startegic Issues-Ensuring a Successful Software Test Strategy, Fundamentals of Software Engineering
The comparison of measuring equipment against a standard instrument of higher accuracy is known as calibration. It is performed to detect, correlate, adjust, rectify and document
the accuracy of the equipment under test. Periodic calibrations are required to detect and correct the error. Periodic calibrations are an integral part of any quality system.
—Continuous Stirred Tank Reactor (CSTR) here is
considered as a nonlinear process. The CSTR is widely used in
many chemical plants. Due to changes in process parameters the
accuracy of final product can be reduced. In order to get accurate
final product the faults developed in CSTR during the chemical
reaction need to be diagnosed. If not, the faults may lead to
degrade the performance of the system. For this purpose there
are various fault diagnosis methods are to be considered. Among
the methods, the neural network predictive controller can be used
to detect faults in CSTR. Servo response is performed to
understand the behavior of CSTR. By detecting various faults
and with suitable control techniques, the accuracy of the
desirable products in CSTR can be improved
Test Strategies for Conventional Software, Unit Testing, Targets for Unit Test Cases, Common Computational Errors in Execution Paths, Other Errors to Uncover, Problems to uncover in Error Handling, Drivers and Stubs for Unit Testing, Fundamentals of Software Engineering
Software Testing Strategies, General Characteristics of Strategic Testing, Verification and Validation, Organizing for Software Testing, A Strategy for Testing Conventional Software, Levels of Testing for Conventional Software, Testing Strategy applied to Conventional Software, Startegic Issues-Ensuring a Successful Software Test Strategy, Fundamentals of Software Engineering
This webinar will provide pesticides residue analysts with valuable information on software method development and data processing for the analysis of pesticide residues in food for both LC–MS and GC–MS. Technical experts will review the latest in software advances to help with data interpretation and reporting.
Speaker at seminar "The Pharmaceutical quality system: ICH Q8/ICH Q9" - University of Parma, 18 May 2012.
Describing steps, tools, and approaches developed for application of QbD to manufacturing processes that have analogous application to the development and use of analytical methods.
This presentation include general introduction to validation of analytical method . analytical method validation include following points such as :
Introduction
Objective ,Types of analytical procedures to be validated,Validation parameters as per ICH and USP , cleaning validation , procedure , validation data, accuracy , range , precision, LOD, LOQ ,linearity, ruggedness , robustness
ICH and WHO Guideline for Validation and Calibration.pptxRAHUL PAL
Validation: Action of proving and documenting that any process, procedure or method actually and consistently leads to the expected results.
Calibration: The set of operations that establish, under specified conditions, the relationship between values indicated by an instrument or system for measuring (for example, weight, temperature and pH), recording, and controlling, or the values represented by a material measure, and the corresponding known values of a reference standard.
Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria or meets the requirements of the client or customer. QC is similar to, but not identical with, quality assurance (QA).
QC IN clinical biochemistry labs and hospitals
The analyst is required to analyze a number of QC samples throughout the run where there are decisions to be made based on a window of acceptance for each QC sample analyzed.
This webinar will provide pesticides residue analysts with valuable information on software method development and data processing for the analysis of pesticide residues in food for both LC–MS and GC–MS. Technical experts will review the latest in software advances to help with data interpretation and reporting.
Speaker at seminar "The Pharmaceutical quality system: ICH Q8/ICH Q9" - University of Parma, 18 May 2012.
Describing steps, tools, and approaches developed for application of QbD to manufacturing processes that have analogous application to the development and use of analytical methods.
This presentation include general introduction to validation of analytical method . analytical method validation include following points such as :
Introduction
Objective ,Types of analytical procedures to be validated,Validation parameters as per ICH and USP , cleaning validation , procedure , validation data, accuracy , range , precision, LOD, LOQ ,linearity, ruggedness , robustness
ICH and WHO Guideline for Validation and Calibration.pptxRAHUL PAL
Validation: Action of proving and documenting that any process, procedure or method actually and consistently leads to the expected results.
Calibration: The set of operations that establish, under specified conditions, the relationship between values indicated by an instrument or system for measuring (for example, weight, temperature and pH), recording, and controlling, or the values represented by a material measure, and the corresponding known values of a reference standard.
Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria or meets the requirements of the client or customer. QC is similar to, but not identical with, quality assurance (QA).
QC IN clinical biochemistry labs and hospitals
The analyst is required to analyze a number of QC samples throughout the run where there are decisions to be made based on a window of acceptance for each QC sample analyzed.
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Memorandum Of Association Constitution of Company.pptseri bangash
www.seribangash.com
A Memorandum of Association (MOA) is a legal document that outlines the fundamental principles and objectives upon which a company operates. It serves as the company's charter or constitution and defines the scope of its activities. Here's a detailed note on the MOA:
Contents of Memorandum of Association:
Name Clause: This clause states the name of the company, which should end with words like "Limited" or "Ltd." for a public limited company and "Private Limited" or "Pvt. Ltd." for a private limited company.
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Registered Office Clause: It specifies the location where the company's registered office is situated. This office is where all official communications and notices are sent.
Objective Clause: This clause delineates the main objectives for which the company is formed. It's important to define these objectives clearly, as the company cannot undertake activities beyond those mentioned in this clause.
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Capital Clause: This clause specifies the authorized capital of the company, i.e., the maximum amount of share capital the company is authorized to issue. It also mentions the division of this capital into shares and their respective nominal value.
Association Clause: It simply states that the subscribers wish to form a company and agree to become members of it, in accordance with the terms of the MOA.
Importance of Memorandum of Association:
Legal Requirement: The MOA is a legal requirement for the formation of a company. It must be filed with the Registrar of Companies during the incorporation process.
Constitutional Document: It serves as the company's constitutional document, defining its scope, powers, and limitations.
Protection of Members: It protects the interests of the company's members by clearly defining the objectives and limiting their liability.
External Communication: It provides clarity to external parties, such as investors, creditors, and regulatory authorities, regarding the company's objectives and powers.
https://seribangash.com/difference-public-and-private-company-law/
Binding Authority: The company and its members are bound by the provisions of the MOA. Any action taken beyond its scope may be considered ultra vires (beyond the powers) of the company and therefore void.
Amendment of MOA:
While the MOA lays down the company's fundamental principles, it is not entirely immutable. It can be amended, but only under specific circumstances and in compliance with legal procedures. Amendments typically require shareholder
Falcon stands out as a top-tier P2P Invoice Discounting platform in India, bridging esteemed blue-chip companies and eager investors. Our goal is to transform the investment landscape in India by establishing a comprehensive destination for borrowers and investors with diverse profiles and needs, all while minimizing risk. What sets Falcon apart is the elimination of intermediaries such as commercial banks and depository institutions, allowing investors to enjoy higher yields.
Implicitly or explicitly all competing businesses employ a strategy to select a mix
of marketing resources. Formulating such competitive strategies fundamentally
involves recognizing relationships between elements of the marketing mix (e.g.,
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2. 1. Purpose: verify QC measuring equipment within acceptable accuracy and
precision investigating measurement system evaluation.
2. REFERENCE:SOP EBV-A52T/F065
EBV-5-1-1/191
3. SCOPE:
EQUIPMENT:LTX SYSTEM
CONTROL ITEM:R&R
→ SAMPLE PARTS MEASURE
ACCURACY & LINEARITY
→ VOLTAGE METER AND SOURCE MEASURE
STANDARD METER: HP3458A
APPRAISE; 31 SYSTEMS
4. METHODOLOGY
4.1 ACCURACY&LINEARITY
4.1.1 Accuracy and linearity can be attained by finding the biases between the true
value and observed value(according to EBV-5-1-1/191)
4.2.2 Action: 26 sets systems
Ext. std meter: HP3458A
Measure coverage: 2.5v ~5.4v
Finished:
By wilson cheng
4.2.3 Accuracy & Linearity procedure file:
DLTA_MSE.XLS
DLTA_DATA.XLS
DLTA_RST.XLS
4.2.4 guide lines for accuracy and linearity (%tolerance analysis)
<5% satisfactory
5% to 10% maybe acceptable need to be investigated
>10% not acceptable
5 Result and Analysis
5.1Accuracy and Linearity
6.Next MSE schedule:
2