The document discusses the qualification of an FTIR analytical instrument. It describes various parameters used to ensure instrument quality such as validation, calibration, and maintenance. Qualification involves collecting evidence that the instrument is suitable for its intended purpose and includes design qualification, installation qualification, operational qualification, and performance qualification phases. The document then discusses specific tests and acceptance criteria for qualifying an FTIR, including tests for resolution, wave number accuracy and reproducibility, transmittance reproducibility, and other tests to evaluate the instrument over time according to ASTM standards.
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
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
This presentation explains about qualifications of HPTLC, types of qualifications, design qualification , installation qualification ,operational qualification, performance qualification ,documentation of qualification .
It is process of “Establishing documentary evidence that provide a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality attributes”.
In the pharmaceutical industry, it is very important that in addition to final testing and compliance of products, it is also assured that the process will consistently produce the expected results.
Validation is action of proving in accordance with the principles of good manufacturing practices, that any procedure, process, equipment, material, activity or system actually leads to expected results.
Cleaning validation is documented evidence with a high degree assurance that one can consistently clean a system or a piece of equipment to predetermined and acceptable limits.
The primary regulatory concern driving the need for cleaning validation is cross contamination of the desired drug substance either by other API from previous batch runs or by residues from the cleaning agents used.
The prime purpose of validating a cleaning process is to ensure compliance with federal and other standard regulations
1. Cross contamination with active ingredients
Contamination of one batch of product with significant levels of residual active ingredients from previous batch cannot be tolerated.
In addition to the obvious problems posed by subjecting consumers or patients to unintended contaminants, potential clinically significant synergistic interactions between pharmacologically active chemicals are a real concern.
2. Contamination with unintended materials or compounds
While inert ingredients used in drug products are generally recognized as safe for human consumption, the routine use, maintenance and cleaning of equipment's provide the potential contamination with such items as equipment parts, lubricants and chemical cleaning agents3. Microbiological contamination
Maintenance , cleaning and storage conditions may provide adventitious microorganisms with the opportunity to proliferate within the processing equipment.
In this slide contains definition and details of Qualification Of HPLC
Presented by: KHALID KUWAITY (Department of pharmaceutical analysis).RIPER, anantapur
QUALIFICATION OF MANUFACTURING EQUIPMENTSANKUSH JADHAV
it gives the information about qualification of various manufacturing equipment which is used into the pharmaceutical labs. (only for information purpose)
In this slide contains introduction, qualification, preventive maintenance, requalification method.
Presented by: Malarvannan M (Department of pharmaceutical analysis).RIPER, anantapur
Qualification of Dissolution Test Apparatus and Validation of Utility System this presentation will help to enhance your knowledge in validation and qualification area.
This presentation explains about qualifications of HPTLC, types of qualifications, design qualification , installation qualification ,operational qualification, performance qualification ,documentation of qualification .
It is process of “Establishing documentary evidence that provide a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality attributes”.
In the pharmaceutical industry, it is very important that in addition to final testing and compliance of products, it is also assured that the process will consistently produce the expected results.
Validation is action of proving in accordance with the principles of good manufacturing practices, that any procedure, process, equipment, material, activity or system actually leads to expected results.
Cleaning validation is documented evidence with a high degree assurance that one can consistently clean a system or a piece of equipment to predetermined and acceptable limits.
The primary regulatory concern driving the need for cleaning validation is cross contamination of the desired drug substance either by other API from previous batch runs or by residues from the cleaning agents used.
The prime purpose of validating a cleaning process is to ensure compliance with federal and other standard regulations
1. Cross contamination with active ingredients
Contamination of one batch of product with significant levels of residual active ingredients from previous batch cannot be tolerated.
In addition to the obvious problems posed by subjecting consumers or patients to unintended contaminants, potential clinically significant synergistic interactions between pharmacologically active chemicals are a real concern.
2. Contamination with unintended materials or compounds
While inert ingredients used in drug products are generally recognized as safe for human consumption, the routine use, maintenance and cleaning of equipment's provide the potential contamination with such items as equipment parts, lubricants and chemical cleaning agents3. Microbiological contamination
Maintenance , cleaning and storage conditions may provide adventitious microorganisms with the opportunity to proliferate within the processing equipment.
In this slide contains definition and details of Qualification Of HPLC
Presented by: KHALID KUWAITY (Department of pharmaceutical analysis).RIPER, anantapur
QUALIFICATION OF MANUFACTURING EQUIPMENTSANKUSH JADHAV
it gives the information about qualification of various manufacturing equipment which is used into the pharmaceutical labs. (only for information purpose)
In this slide contains introduction, qualification, preventive maintenance, requalification method.
Presented by: Malarvannan M (Department of pharmaceutical analysis).RIPER, anantapur
Qualification of Dissolution Test Apparatus and Validation of Utility System this presentation will help to enhance your knowledge in validation and qualification area.
qualification of instrument(UV & FTIR) BY Bhumi Suratiya, M.Pharm sem 2.pptxBhumiSuratiya
So, Here it's presentation on Qualification of instrument(UV & FTIR) BY Bhumi Suratiya, M.Pharm sem 2. Qualification of analytical instruments. it also includes design qualifications (DQ), Installation qualification(IQ)
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QUALIFICATION OF UV-VISIBLE SPECTROPHOTOMETER, FTIR, DSC, HPLCAnupriyaNR
Analytical method qualification consists of a simplified evaluation of a subset of validation characteristics with a goal to demonstrate that an analytical method is scientifically sound and suitable for its intended use. In contrast to validation, analytical method qualification is performed without predefined acceptability criteria. Qualification may be performed as a prerequisite to method validation, or when an assay for product knowledge has not yet been established as a test for a critical product quality attribute. Qualification of equipment is pre-requisite for validation of the process in which the equipment is being used. Many types of equipment have measuring devices on them. Calibration of measuring devices is a part of qualification. Calibration of measuring devices is important, as the data is often collected through them. If the data collected is not from measuring devices that have been calibrated, the data cannot be relied upon. Thus the whole validation exercise can be questioned.
Calibration is the activity of checking, by comparison with a standard, the accuracy of a measuring instrument of any type. It may also include adjustment of the instrument to bring it into alignment with the standard
DATION OF EQUIPMENT ICH AND WHO GUIDELINES FOR CALIBRATION AND VALIDATION OF ...deepalisanap31
Introduction to equipment
Calibration
ICH guidelines for calibration of equipment
WHO guidelines for calibration of equipment
Example for calibration of UV
Validation
ICH guidelines for validation of equipment
WHO guidelines for validation of equipment
Example for validation of tablet compression machine
A validation programme involves various components in pharmaceutical organisation related to process, equipment and product.
It is a regulatory requirement for pharmaceutical companies to perform Instrument Validation on all new instruments.
Instrument Validation requires detailed knowledge of the instrumentation system being validated and is therefore usually performed by the company supplying the instrument.
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June 3, 2024 Anti-Semitism Letter Sent to MIT President Kornbluth and MIT Cor...Levi Shapiro
Letter from the Congress of the United States regarding Anti-Semitism sent June 3rd to MIT President Sally Kornbluth, MIT Corp Chair, Mark Gorenberg
Dear Dr. Kornbluth and Mr. Gorenberg,
The US House of Representatives is deeply concerned by ongoing and pervasive acts of antisemitic
harassment and intimidation at the Massachusetts Institute of Technology (MIT). Failing to act decisively to ensure a safe learning environment for all students would be a grave dereliction of your responsibilities as President of MIT and Chair of the MIT Corporation.
This Congress will not stand idly by and allow an environment hostile to Jewish students to persist. The House believes that your institution is in violation of Title VI of the Civil Rights Act, and the inability or
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The House of Representatives will not countenance the use of federal funds to indoctrinate students into hateful, antisemitic, anti-American supporters of terrorism. Investigations into campus antisemitism by the Committee on Education and the Workforce and the Committee on Ways and Means have been expanded into a Congress-wide probe across all relevant jurisdictions to address this national crisis. The undersigned Committees will conduct oversight into the use of federal funds at MIT and its learning environment under authorities granted to each Committee.
• The Committee on Education and the Workforce has been investigating your institution since December 7, 2023. The Committee has broad jurisdiction over postsecondary education, including its compliance with Title VI of the Civil Rights Act, campus safety concerns over disruptions to the learning environment, and the awarding of federal student aid under the Higher Education Act.
• The Committee on Oversight and Accountability is investigating the sources of funding and other support flowing to groups espousing pro-Hamas propaganda and engaged in antisemitic harassment and intimidation of students. The Committee on Oversight and Accountability is the principal oversight committee of the US House of Representatives and has broad authority to investigate “any matter” at “any time” under House Rule X.
• The Committee on Ways and Means has been investigating several universities since November 15, 2023, when the Committee held a hearing entitled From Ivory Towers to Dark Corners: Investigating the Nexus Between Antisemitism, Tax-Exempt Universities, and Terror Financing. The Committee followed the hearing with letters to those institutions on January 10, 202
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3. Introduction
A simple apparatus to complex computerized systems, is used in the
pharmaceutical industry to acquire data that will help ensure that
products meet their specifications.
Qualification, calibration, validation, and maintenance are the
parameters used to demonstrate that an instrument is qualified and
under control.
Generally, the more complex the instrument, or the higher the criticality
of the measurement, the greater the amount of work that is required to
ensure that quality data will be generated. In addition, attention must be
paid to ensuring that data integrity and security are maintained.
Instruments can generally be classified as belonging to Groups A, B, or
C. It should be noted that the same type of instrument can fit into one or
more categories, depending on its intended use.
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6. Analytical Instrument Qualification:
AIQ is the collection of documented Evidence that an
instrument performs suitably for its intended purpose.
Analytical Method Validation:
Analytical method validation is the collection of documented
evidence that an analytical procedure is suitable for its intended
use.
System Suitability Tests:
System suitability tests verify that the system will perform in
accordance with the criteria set forth in the procedure.
Quality Control Check Samples:
Many analysts carry out their tests on instruments that have
been standardized by using reference materials and/or calibration
standards.
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7. VALIDATION
It is a act of demonstrating and documenting that the process operates
effectively and reproducibly to produce a product meeting its
predetermined specifications and quality attributes.
The aim of validation is to show that the critical steps are under
control and lead continuously to the desirable quality.
CALIBRATION
Calibration is a comparison between measurements – one of known
magnitude or correctness made or set with one device and another
measurement made in as similar a way as possible with a second
device.
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8. QUALIFICATION:
Qualification is an act or process to assure something complies with some
conditions, standard or specific requirements.
Qualification Phases
The qualification phases consist of mainly 5 phases.
Its start with User requirement specification (URS).
URS is a document which states the laboratory requirement and technical
and operational requirements that should be met.
The other phases consist of
Design Qualification (DQ)
Installation Qualification (IQ)
Operational Qualification (OQ)
Performance Qualification (PQ)
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9. Apart from URS, DQ, IQ, OQ and PQ; some other parameters are
to be performed such as Factory acceptance test (FAT) and site
acceptance test (SAT) where applicable.
When the instrument undergoes major repairs or modifications,
this should be evaluated using change control.
Relevant IQ,OQ, and/or PQ tests should be repeated to verify that
the instrument continues to operate satisfactorily.
If an instrument is moved to another location, an assessment
should be made of what, if any, qualification stage should be
repeated.
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10. • Design Qualification:
Documented evidence which shows that the plant design agrees
with the design specifications of the customer.
• Installation Qualification:
Written evidence is given that all parts of equipment are installed according to
the equipment supplier’s and purchase specifications.
• Operational qualification:
Documented evidence which shows that all parts of the plant and equipment
work within their specifications and process parameters.
• Performance Qualification:
Provides documented evidence that all parts of a plant and other processes
produce products of specified quality under conditions of normal production
for a longer period of time.
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11. FTIR
Fourier transform infrared spectroscopy (FTIR) is a technique which is
used to obtain an infrared spectrum of absorption, emission,
photoconductivity or Raman scattering of a solid, liquid or gas.
An FTIR spectrometer simultaneously collects spectral data in a wide
spectral range. This confers a significant advantage over a dispersive
spectrometer which measures intensity over a narrow range of
wavelengths at a time.
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12. CALIBRATION
WAVE NUMBER PRESCISION:
• This is performed for substances with well known peak wave number(s)
position such as carbon dioxide, water vapour, polystyrene ,ammonia.
• Test is performed to know whether the exact peak wave numbers are
shown at that time of validation.
• Thus the result is obtained from the difference between the peak wave
numbers position for a substance with a well known peak wave numbers
and the values indicated by the system.
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13. 0% TRANSMITTANCE:
• A sample which do not allow the transmission of light is measured in
order to investigate the 0% transmittance.
• This test thus can be used to find out error caused by stray light and
secondary emission spectra.
100% TRANSMITTANCE
• This is investigated by performing analysis with out a sample.
• By performing analysis with out the sample 100% transmittance can be
investigated.
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14. LINEARITY OF CURVE:
A calibration curve for the % transmittance and the
concentration is created and the linearity of the inspected.
REPRODUCIBILITY:
A stable sample is measured twice with in a short period and confirmed
whether the variation in the measurement values such as wave numbers
and transmittance are obtained.
VALIDATION OF FTIR:
• To perform FTIR validation and to confirm
that it is operating properly, diverse IR inspection
was performed by measuring the spectra of polystyrene film.
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15. INSTALLATION OF VALIDATION PROGRAMME
• Software validates the Shimadzu Fourier transform
infrared spectrophotometer IRPrestige-21/IRAffinity1/
FTIR-8000 series by the IR solution software to control them and data
processing
• The Validation program is automatically installed when the IR
solution is installed, therefore the Validation program does not need to
be separately installed.
PERFORMANCE QUALIFICATION
• POWER SPECTRUM
• Power spectrum gives the plot of portion of signal's power(energy per
unit time) falling with in the given frequency bins.
• This test estimates the intensity of power spectrum at a specified
wave numbers .
• When the measured intensity is equal to or larger than the criterion
value, the test is passed.
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17. RESOLUTION
• The resolution is checked by recording the spectrum of polystyrene film of
approximately 35µm in thickness.
• The difference between percentage transmittance at the absorption
maximum A at 2870 cm-1 and absorption minima B at 2849.5 cm-1 must
be greater than 18.
• The difference between percentage transmittance at the absorption
maximum C at 1589 cm-1 and absorption minima D at 1583 cm-1 must be
greater than 12.
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18. WAVE NUMBER ACCURACY
• The wave number scale is usually calibrated by the
use of several characteristic wave numbers of a polystyrene film.
3060.0(+/-1.5) cm-1
2849.5(+/-1.5) cm-1
1942.9(+/-1.5) cm-1
1601.2(+/-1.0) cm-1
1583.0(+/-1.0) cm-1
1154.5(+/-1.0) cm-1
1028.3(+/-1.0) cm-1
• The software then judges whether the values are within in the allowable
range.
• The program labels the results “PASS” if all the peak numbers are within
the range.
• In case of dispersive spectrophotometer the permissible level of frequency
at 1601.2 cm-1 and at 1028.3 cm-1 should be with in +/- 2.0 cm-1.
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19. WAVE NUMBER REPRODUCIBILTY
• This program specifies three points to measure the peak wave numbers.
• Then it obtains the actual peak wave numbers at each point by measuring
the polystyrene film twice.
• It should satisfy 5 cm-1 around 3000 cm-1of polystyrene absorption wave
number,1 cm-1 around 1000 cm-1.
• The software determines whether the differences between each of two
measurements are within the allowable range and it labels the result PASS if
they are with in the range.
• EP 4.0 doesn’t include this inspection
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20. TRANSMITANCE REPRODUCIBILTY
• This program specifies peak wave number at three points and the
transmittance at each point is measured is twice.
• The transmittance reproducibility should satisfy 0.5%T when the
several points of polystyrene absorption from 3000 cm-1to 1000 cm-1are
measured twice.
• Then it is determined whether the differences between the two data
are within the allowable range and it labels the result PASS if they are
with in the range.
• All of the above furnished data should be represented in
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21. AS PER ASTM E1421-94 Level Zero
• This soft ware complies describes with in the description in the
ASTM(American Society for Testing and materials).
• The FTIR abnormalities or large changes over short term and
long term is assessed by these tests.
• The three parameters checked by this program are:
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22. ENERGY SPECTRUM TEST
Power spectra obtained in the inspection are compared with
reference data and the spectra are checked for changes over long
periods.
ONE HUNDRED PERCENT LINE TEST
100% T line spectra are calculated for power spectra & are measured
continuously in inspection and the spectra are checked for changes
over short periods.
POLYSTYRENE TEST
Evaluation is performed using differences between spectra obtained
for polystyrene film in inspection and the stored reference data.
When the differences are with in the standard, "pass” results.
All of the above furnished data should be represented in Validation
Report.
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