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
Reference standards in Pharmaceutical Industriesbhavanavedantam
This presentation is brief introduction about reference standards that are using in pharmaceutical industries for calibration of different instruments, methods and pharmaceutical chemicals...
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
Reference standards in Pharmaceutical Industriesbhavanavedantam
This presentation is brief introduction about reference standards that are using in pharmaceutical industries for calibration of different instruments, methods and pharmaceutical chemicals...
Analytical method validation as per ich and usp shreyas B R
Analytical method validation is a process of documenting/ proving that an analytical method provides analytical data acceptable for the intended use.After the development of an analytical procedure, it is must important to assure that the procedure will consistently produce the intended a precise result with high degree of accuracy. The method should give a specific result that may not be affected by external matters. This creates a requirement to validate the analytical procedures. The validation procedures consists of some characteristics parameters that makes the method acceptable with addition of statistical tools.
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
Analytical method validation, ICH Q2 guidelineAbhishek Soni
Analytical Method Validation, ICH Q2 Guideline.
General principles related to the analytical method validation.
Validation of analytical method as per International Council for Harmonisation(ICH) guidelines and the United States Pharmacopeia(USP).
Glossary.
Useful in understanding the terms :
Specificity
Linearity
Range
Accuracy
Precision
Detection limit
Quantitation limit
Robustness
Ruggedness
System suitability testing
Validation: Validation is a documented program that provides high degree of assurance that a specific process, method or system consistently produces a result meeting pre-determined acceptance criteria.
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)
Analytical method validation as per ich and usp shreyas B R
Analytical method validation is a process of documenting/ proving that an analytical method provides analytical data acceptable for the intended use.After the development of an analytical procedure, it is must important to assure that the procedure will consistently produce the intended a precise result with high degree of accuracy. The method should give a specific result that may not be affected by external matters. This creates a requirement to validate the analytical procedures. The validation procedures consists of some characteristics parameters that makes the method acceptable with addition of statistical tools.
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
Analytical method validation, ICH Q2 guidelineAbhishek Soni
Analytical Method Validation, ICH Q2 Guideline.
General principles related to the analytical method validation.
Validation of analytical method as per International Council for Harmonisation(ICH) guidelines and the United States Pharmacopeia(USP).
Glossary.
Useful in understanding the terms :
Specificity
Linearity
Range
Accuracy
Precision
Detection limit
Quantitation limit
Robustness
Ruggedness
System suitability testing
Validation: Validation is a documented program that provides high degree of assurance that a specific process, method or system consistently produces a result meeting pre-determined acceptance criteria.
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)
Undertand requirements of normality in ANSI/ASQ Z1.9 and how that affects analysis of meter test data.
Review typical meter test data distributors and how to determine if meter test data is normal
Introduction to working with non-normal data
NDSRIs - Nitrosamine Drug Substance-Related Impurities (NDSRIs)Chandra Prakash Singh
NDSRIs impurities share structural similarity to the API (having the API or API fragment in the chemical structure) and are therefore unique to each API.
NDSRIs generally form in the drug product through nitrosation of APIs (or API fragments) that have secondary or tertiary amines when exposed to nitrosating agents such as residual nitrites in excipients used to formulate the drug product.
Generally, the presence of high levels of NDSRIs has been associated with drug products rather than APIs because NDSRI formation usually results from a reaction between the API or API fragment and nitrosating agents in the drug formulation.
However, NDSRIs can potentially form in APIs when nitrosating agents are present in the API manufacturing process or when APIs undergo processing steps that can potentially induce their formation such as fluid bed drying at an elevated temperature and jet milling because these can create favorable conditions in which nitrogen oxides can react with at-risk APIs.
NDSRIs often lack carcinogenicity and mutagenicity study data (typically from animal studies) from which an AI limit can be determined.
This guidance provides a recommended methodology for AI limit determination that uses structural features of NDSRIs to generate a predicted carcinogenic potency categorization and corresponding recommended AI limit that manufacturers and applicants can apply, in the absence of other FDA recommended AI limits, in their evaluations of approved and marketed drug products as well as products in development or under review by FDA.
Currently Identified Risk Factors for Presence of Nitrosamines.pptxChandra Prakash Singh
N-Nitrosamines can be formed when an amine and nitrosating agent are combined under favourable conditions although other generation pathways are also possible, such as e.g. oxidation and reduction processes from hydrazine-type compounds and N-nitro derivatives.
Root causes for N-nitrosamines in medicinal products identified to date can be grouped as risk factors linked exclusively with the manufacturing process and storage of active substance and/or as risk factors associated with manufacture and storage of the finished product.
Moreover, there are risk factors specifically linked to GMP aspects.
Basic Understanding of LCMS
Ion Optics Path and Parameters.
Mass spectrometry measures the mass-to-charge ratio of ions to identify unknown compounds, to quantify known compounds, and to provide information about the structural and chemical properties of molecules.
The mass spectrometer has a series of quadrupole filters that transmit ions according to their mass-to-charge (m/z) ratio.
When the energy of the accelerated electrons is higher than a certain threshold value (which depends on the metal anode), a second type of spectrum is obtained superimposed on top of the white radiation. It is called the characteristic radiation and is composed of discrete peaks.
The energy (and wavelength) of the peaks depends solely on the metal used for the target and is due to the ejection of an electron from one of the inner electron shells of the metal atom.
This results in an electron from a higher atomic level dropping to the vacant level with the emission of an X-ray photon characterised by the difference in energy between the two levels.
CHARACTERIZATION OF CRYSTALLINE AND PARTIALLY CRYSTALLINE SOLIDS BY X-RAY POWDER DIFFRACTION (XRPD)
USP <941>
Every crystalline phase of a given substance produces a characteristic X-ray diffraction pattern.
Diffraction patterns can be obtained from a randomly oriented crystalline powder composed of crystallites (crystalline regions within a particle) or crystal fragments of finite size.
Essentially three types of information can be derived from a powder diffraction pattern:
The angular position of diffraction lines (depending on geometry and size of the unit cell).
The intensities of diffraction lines (depending mainly on atom type and arrangement and preferred orientation within the sample.
Diffraction line profiles (depending on instrumental resolution, crystallite size, strain, and specimen thickness).
LCMS - Ion Optics Path and Parameters
Source and gas parameters: These parameters can change depending on the ion source used.
Compound parameters: These parameters consist mostly of voltages in the ion path. Optimal values for compound-dependent parameters vary depending on the compound being analyzed.
Resolution parameters: These parameters affect the resolution and calibration.
Detector parameters: These parameters affect the detector.
A divert valve allows you to switch portions of the mobile phase to waste before the mass spectrometer.
This is particularly important for the portion containing all the un-retained components – many of which are likely to be involatile and contaminate the source. If you really want to keep things clean use a divert valve to divert everything to waste except the compounds of interest.
The integrated diverter valve, which is located next to the ion source, can be plumbed in injector mode or diverter mode.
LCMS Interface
API techniques (ESI, APCI and APPI)
In LCMS, ions can be generated through either the continuous or pulsed (discontinuous) modes.
The three API techniques (ESI, APCI and APPI) that were introduced operates in the continuous mode, giving a constant flow/supply of ions to the MS.
On the other hand, the pulsed mode generates a discontinuous source of ions such as the Matrix-Assisted Laser Desorption/Ionization (MALDI).
Analytical control strategy - Part -4 : How the ACS Applies to the Product Lifecycle and How the modern concept of a lifecycle model can be applied to analytical procedures.
How the modern concept of a lifecycle model, which is based on process validation and described in ICH guidelines Q8, Q9, and Q10, can be applied to analytical procedures.
Biological screening of herbal drugs: Introduction and Need for
Phyto-Pharmacological Screening, New Strategies for evaluating
Natural Products, In vitro evaluation techniques for Antioxidants, Antimicrobial and Anticancer drugs. In vivo evaluation techniques
for Anti-inflammatory, Antiulcer, Anticancer, Wound healing, Antidiabetic, Hepatoprotective, Cardio protective, Diuretics and
Antifertility, Toxicity studies as per OECD guidelines
A review of the growth of the Israel Genealogy Research Association Database Collection for the last 12 months. Our collection is now passed the 3 million mark and still growing. See which archives have contributed the most. See the different types of records we have, and which years have had records added. You can also see what we have for the future.
Normal Labour/ Stages of Labour/ Mechanism of LabourWasim Ak
Normal labor is also termed spontaneous labor, defined as the natural physiological process through which the fetus, placenta, and membranes are expelled from the uterus through the birth canal at term (37 to 42 weeks
Operation “Blue Star” is the only event in the history of Independent India where the state went into war with its own people. Even after about 40 years it is not clear if it was culmination of states anger over people of the region, a political game of power or start of dictatorial chapter in the democratic setup.
The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
Acetabularia Information For Class 9 .docxvaibhavrinwa19
Acetabularia acetabulum is a single-celled green alga that in its vegetative state is morphologically differentiated into a basal rhizoid and an axially elongated stalk, which bears whorls of branching hairs. The single diploid nucleus resides in the rhizoid.
Macroeconomics- Movie Location
This will be used as part of your Personal Professional Portfolio once graded.
Objective:
Prepare a presentation or a paper using research, basic comparative analysis, data organization and application of economic information. You will make an informed assessment of an economic climate outside of the United States to accomplish an entertainment industry objective.
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
Executive Directors Chat Leveraging AI for Diversity, Equity, and InclusionTechSoup
Let’s explore the intersection of technology and equity in the final session of our DEI series. Discover how AI tools, like ChatGPT, can be used to support and enhance your nonprofit's DEI initiatives. Participants will gain insights into practical AI applications and get tips for leveraging technology to advance their DEI goals.
2024.06.01 Introducing a competency framework for languag learning materials ...Sandy Millin
http://sandymillin.wordpress.com/iateflwebinar2024
Published classroom materials form the basis of syllabuses, drive teacher professional development, and have a potentially huge influence on learners, teachers and education systems. All teachers also create their own materials, whether a few sentences on a blackboard, a highly-structured fully-realised online course, or anything in between. Despite this, the knowledge and skills needed to create effective language learning materials are rarely part of teacher training, and are mostly learnt by trial and error.
Knowledge and skills frameworks, generally called competency frameworks, for ELT teachers, trainers and managers have existed for a few years now. However, until I created one for my MA dissertation, there wasn’t one drawing together what we need to know and do to be able to effectively produce language learning materials.
This webinar will introduce you to my framework, highlighting the key competencies I identified from my research. It will also show how anybody involved in language teaching (any language, not just English!), teacher training, managing schools or developing language learning materials can benefit from using the framework.
A Strategic Approach: GenAI in EducationPeter Windle
Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
2. Ordinary name
Number of digits
after
decimal position
(g)
Accuracy
Class
d value
(g)
Minimum weight
Ultra Micro Balances 7 I 0.0000001 0.082 mg*
Micro Balances 6 I 0.000001 0.82 mg
Semi-micro Balances 5 I 0.00001 8.2 mg
Analytical Balances 4 I 0.0001 82 mg
Precision Balances 1 to 3 II 0.001$ 820 mg$
Technical Balances 0 to 1 III 1$$ 82000 mg /820 g$$
Classification of Balance
*Minimum weight = (2000 × 0.41d) = 2000 x 0.41 x 0.0000001 = 0.000082 g = 0.082 mg
$ for Number of digits after decimal position (g) = 3
$ $ for Number of digits after decimal position (g) = 0
3. Class Maximum Permissible Error (MEP) % MEP
Suitable for weighing
instruments
Class E1 from nominal value at1 kg is < 0.5mg 0.00005 --
Class E1 weights are the highest accuracy class, and are intended to be used for traceability
between national mass standards and OIML class.
Class E2 from nominal value at 1kg is <1.6mg. 0.00016 Accuracy class I
Class F1 from nominal value at 1kg is <5mg. 0.0005 Accuracy class I
Class F2 from nominal value at 1kg is <16mg. 0.0016 Accuracy class II
Class M1 from nominal value at 1kg is <50mg. 0.005 Accuracy class II
Class M2 from nominal value at 1kg is <160mg. 0.016 Accuracy class III
Class M3 from nominal value at 1kg is <500mg. 0.05 Accuracy class III
Classification of Weights
(as per International Organization of Legal Metrology (OIML))
Each class specifies maximum permissible errors from a range of nominal conventional
mass values, but the classification that can be given to a weight also depends up on its
material, density, corrosion resistance, hardness, wear resistance, brittleness, magnetic
properties, construction and surface finish.
4. This chapter states the requirements for balances used for materials that must be
“accurately weighed”.
USP General Chapters <41> BALANCES
Unless otherwise specified, when substances must be “accurately weighed,” the weighing
shall be performed using a balance that is calibrated over the operating range and
meets the requirements defined for repeatability and accuracy.
5. Accuracy:
The accuracy of a balance is satisfactory if its weighing value, when tested with a suitable
weight(s), is within 0.10% of the test weight value.
USP General Chapters <41> BALANCES
Accuracy
Balance Capacity Accuracy test weight range (5% to 100%)
200 g 10 g to 200 g
Test Weight :
1. A test weight is suitable if it has a mass between 5% and 100% of the balance's
capacity.
2. The test weight's maximum permissible error (mpe), or alternatively its calibration
uncertainty, shall be NMT one-third of the applied test limit of the accuracy test.
6. Repeatability:
Ability of a weighing instrument to display identical measurement values for repeated
weighings of the same objects under the same conditions, e.g., the same measurement
procedure, same operator, same measuring system, same operating conditions, and same
location over a short period of time. Repeatability usually is expressed as the standard
deviation of multiple weighings.
Repeatability is assessed by weighing one test weight NLT 10 times.
USP General Chapters <41> BALANCES
Repeatability
Test Weight:
1. Test weight should be a few percent of the nominal capacity of the balance.
2. The test weight must be within the balance‘s operating range, but the weight need not
be calibrated. Because the standard deviation is virtually independent of sample mass
within the balance's capacity.
3. Use of a small test weight, which may be difficult to handle, is not required.
7. Calculation
Repeatability = (2 × (standard deviation or 0.41d))/Desired smallest net weight
USP General Chapters <41> BALANCES
Repeatability
Acceptance criteria:
Case I: If the standard deviation is more than 0.41d (where d is the scale interval)
Repeatability is satisfactory if two times the standard deviation of the weighed value,
divided by the desired smallest net weight (i.e., smallest net weight that the users plan to use
on that balance), does not exceed 0.10%.
Case II: If the standard deviation is more than 0.41d (where d is the scale interval)
Repeatability is satisfactory if 2×0.41d, divided by the desired smallest net weight, does not
exceed 0.10%.
8. USP 40 and USP41 - Repeatability
Repeatability is satisfactory if two times the standard deviation of the weighed value,
divided by the desired smallest net weight (i.e., smallest net weight that the users plan to
use on that balance), does not exceed 0.10%. If the standard deviation obtained is less
than 0.41d, where d is the scale interval, replace this standard deviation with 0.41d. In this
case, repeatability is satisfactory if 2 × 0.41d, divided by the desired smallest net weight,
does not exceed 0.10%.
USP General Chapters <41> BALANCES
The change made in USP for measurement of Repeatability
USP 37 - Repeatability
Repeatability is satisfactory if two times the standard deviation of the weighed value,
divided by the nominal value of the weight used, does not exceed 0.10%. If the standard
deviation obtained is less than 0.41d, where d is the scale interval, replace this standard
deviation with 0.41d. In this case, repeatability is satisfactory if two times 0.41d, divided
by the nominal value of the weight used, does not exceed 0.10%.
9. Performance Qualification:
1. The tests should be recorded in such a manner that the data can be used to easily track
balance performance and to assist in laboratory investigations as needed.
2. Meaningful acceptance criteria can be set depending on the required weighing
tolerance, i.e., the maximum allowed deviation permitted by specifications,
regulations, etc., of a quantity to be weighed from its target value.
3. Procedures should be in place to address test results that are outside acceptable ranges
and to provide assurance that balance cleanliness and environment have not affected
the result.
4. Also, a procedure should be in place for removing a balance from operation when
observed results fall outside acceptable ranges.
USP General Chapters <1251> Weighing on an Analytical Balance
10. Property Definition Examples Acceptance Criteria
Sensitivity
Change in the displayed value
divided by the load on the
balance, which causes
this change.
The test load at or sufficiently
close to the capacity of the
balance.
NMT 0.05% deviation from 1
(the sensitivity of a correctly
adjusted balance), where
<41> is applicable. For other
uses, respective tolerance
requirement divided by 2.
Linearity
Ability of a balance to follow
the linear relationship
between a load and the
indicated weighing value.
Nonlinearity usually is
expressed as the largest
magnitude of any linearity
deviation within the test
interval.
From 3 to 6 points over the
range of the balance.
NMT 0.05% deviation where
<41> is applicable. For other
uses, respective tolerance
requirement divided by 2.
USP General Chapters <1251> Weighing on an Analytical Balance
Performance Tests and Acceptance Criteria
11. Property Definition Examples Acceptance Criteria
Eccentricity
Deviation in the measurement
value caused by eccentric
loading in other words, the
asymmetrical placement of
the center of gravity of the
load relative to the load
receiver. Eccentricity usually
is expressed as the largest
magnitude of any of the
deviations between an off
center reading and the center
reading for a given test load.
Performed in the center of
gravity and the four quadrants
(for rectangular platter
shapes) or at analogous
locations for other platter
shapes. Test load usually
should be 30% of the capacity
of the balance or higher (refer
to the manufacturer's manual
for any possible upper
limit).
NMT 0.05% deviation where
<41> is applicable.
For other uses, respective
tolerance requirement divided
by 2.
Repeatability
Repeatability usually is
expressed as the standard
deviation of multiple
weighings.
10 replicate weighings (using
a test weight that is a few
percent of the nominal
capacity of the balance).
Requirement from <41>
where applicable.
For other uses, user specified
requirements will apply.
Performance Tests and Acceptance Criteria
12. Sensitivity, linearity, and eccentricity all account for systematic deviations; i.e., they limit
the accuracy of the balance (based on the definition of accuracy in Validation of
Compendial Procedures <1225> and ICH Q2). In the International Vocabulary of
Metrology (VIM) and documents of the International Organization for Standardization, this
concept is referred to as trueness.
Performance Tests
Because deviations are largely independent from each other, it is not likely that all
deviations occur simultaneously and have the same algebraic sign. Therefore the
arithmetic addition of all individual deviations to assess the balance accuracy would
constitute a rather conservative approach. A quadratic addition of the individual deviations
is a more realistic approach.
By allocating 50% of the weighing tolerance budget to the acceptance criteria of the
individual properties, e.g., sensitivity, linearity, and eccentricity, analysts ensure adherence
to the required weighing tolerance. Therefore, the acceptance criteria for the individual
properties that account for the systematic deviations are set to weighing tolerance divided
by 2.
13. Depending on the acceptance criterion, it may be sufficient to consider only the nominal
weight value of the test weights. If the nominal value of the test weight is considered,
analysts should ensure that the maximum permissible error does not exceed one-third of the
acceptance criterion.
Alternatively, if the certified value of the test weight is considered, its calibration uncertainty
should not exceed one-third of the acceptance criterion.
If more than one weight is used to perform the test, the calibration uncertainties of the
weights must be summed and the sum should not exceed one-third of the acceptance
criterion.
Performance Tests
Repeatability preferably is tested with a test weight of a few percent of the balance capacity.
At the lower end of its measurement range, the performance of laboratory balances is limited
by the finite repeatability, and limitations induced by systematic deviations normally can be
neglected. Therefore, the whole weighing tolerance budget can be allocated to the
acceptance criterion of the repeatability test.
For tests such as eccentricity or repeatability, the use of certified weights is optional, but
analysts must ensure that the mass of the weight does not change during the test.
14. The minimum net sample weight, in short, minimum weight, mmin, of an analytical
balance can be expressed by the equation:
Minimum Weight
In order to satisfy the required weighing tolerance, when samples are weighed the amount of
sample mass (i.e., the net weight) must be equal to or larger than the minimum weight. The
minimum weight applies to the sample weight, not to the tare or gross weight.
Simplified Formula
mmin = (2 x (s or 0.41d) x 100)/0.1
= 2000 × (s or 0.41d)
mmin = k × s/required weighing tolerance
where
k = is the coverage factor (usually 2 or larger)
S = is the standard deviation (in a mass unit, e.g., in mg) of NLT 10 replicate
measurements of a test weight. If the standard deviation obtained is less than 0.41d,
where d is the scale interval, the standard deviation is replaced by 0.41d.
Required weighing tolerance = 0.1%
15. The lower limit of 0.41d for the standard deviation results from the rounding error of the
digital indication of a weighing instrument. The rounding error that is allocated to a single
reading is calculated as 0.29d.
Minimum Weight
The minimum weight describes the lower limit of the balance below which the required
weighing tolerance is not adhered to.
Note that a weighing always consists of two readings, one before and one after
placing/removing the sample on/from the pan, with the difference between the two
indications being the net sample weight. The two individual rounding errors are usually
added quadratically, leading to 0.41d.
Taring the instrument after placing the tare container on the pan does not affect the rounding
error as the zero indication is also rounded.
16. LOCATION
1. The balance should be located in a room that is temperature and humidity controlled.
2. The location should have a clean, consistent electrical power supply.
3. The location should be free of drafts and should not be near ovens, furnaces, air
conditioner ducts, or cooling fans from equipment or computers.
4. The balance should be positioned away from outside windows so that direct sunlight
does not strike the balance.
5. The balance should not be installed near sources of electromagnetic radiation such as
radio-frequency generators, electric motors, or hand-held communication devices
(including cordless telephones, cellular telephones, and walkie-talkies).
6. The balance should not be located near magnetic fields induced by laboratory
instrumentation or other equipment.
Support Surface & Location
SUPPORT SURFACE
The balance should be installed on a solid, level, nonmagnetic surface that minimizes
the transmission of vibration (e.g., a floor-mounted, granite weigh bench). If a metallic
support surface is used, the surface should be grounded in order to prevent
the buildup of static electricity.