Who uses reference materials?
Reference materials are a critical component of the analytical testing workflow. Through calibration of measurement systems, validation of methods, and quality control programs, reference materials ensure accuracy in testing. From certified reference materials (CRMs) and other quality grades of reference materials, to certificates of analysis, metrological traceability and other concepts, the world of reference materials is vast, and at times, confusing.
These charts present critical reference material topics, offering information on metrological traceability, the hierarchy of reference materials, certificates of analysis, reference material formats and uses, and fit-for-purpose selection considerations. Proper selection of the right reference material for the laboratory’s testing application is important, because results are only as accurate as your reference.
Figure 1. Metrological Traceability – SI Unit of Measurement
Metrological traceability and SI Units of your reference materials
Metrological traceability is an important concept in the world of reference materials. A fundamental term in metrological traceability is the SI unit of measurement. The International System of Units, or SI, defines the seven units of measure as the basic set from which all other SI units can be derived. The two most common SI units of measure for traceability of reference materials are kilogram and mole.
Metrological traceability means measurements can be meaningfully compared, across difference places, at different times, by different people, using different equipment. The measurement result must be related to a reference through a documented and unbroken chain of calibrations, tracing back to the SI unit of measurement.
ISO 17034 and quality grades of standards, reference materials and certified reference materials
National Metrology Standard (e.g. NIST, JRC, NMI Australia)
Compendial Standard (e.g. USP, EP, BP, JP, IP) Issued by an authorized body Considered to provide the highest level of accuracy & traceability Certified Reference Material (CRM) (ISO 17034, 17025) Considered to provide the highest level of accuracy, uncertainty, and traceability to an SI unit of measurement Manufactured by an accredited Reference Material Producer Reference Material (RM) (ISO 17034) Fulfilling ISO requirements which are less demanding than for CRMs Manufactured by an accredited Reference Material Producer
Analytical Standard (ISO 9001) Certificate of Analysis available Level of certification varies
Reagent Grade / Research Chemical May come with a Certificate of Analysis Are not characterised for use as reference materials
Figure 2. The Hierarchy of Reference Materials – What are the Different Types?
The reference material hierarchy includes five major quality grades, from national metrology and other primary standards to Certified Reference Materials (CRMs), Reference Materials (RMs), Analytical Standards, and research grade or research chemicals. Level of certification and traceability requirements increase for each higher level. Where national governments give standardization to the top level, specific ISO guidelines provide standardization for CRMs and RMs. These ISO requirements include ISO 17034, ISO/IEC 17025 and ISO Guide 31.
Reference material producers must meet these ISO requirements to manufacture CRMs or RMs. For both of these quality grades, Certificates of Analysis must be provided, and the information contained within is defined by the aforementioned ISO guidelines. The quality specifications for the last two levels are defined by each individual producer rather than by a national government or ISO accreditations specific to CRMs and RMs.
What is measured in each grade of reference material?
Purity and Identity of the material are typically included in the Certificate of Analysis for each of the five quality grades. Content and Stability are required for the primary standards or ISO-defined CRM and RM.
Analytical standards and research chemicals may or may not include these two parameters as their inclusion is dependent on the producer. Analytical Standards can also in some cases be Quality Control materials compliant with ISO Guide 80.
Homogeneity is required for the primary standards, CRM, and RM, but this parameter will not be found with the lower quality grades. Uncertainty and Traceability information are limited to just the primary standards and CRM. In the pharmaceutical world, secondary standards can be CRMs or RMs, but here, there are two different types of traceability – to the SI unit of measurement for the ISO-defined CRM as well as traceability to the primary compendial standard, which is a requirement specific to pharmaceutical secondary standards.
Table 1. The Hierarchy of Reference Materials – What’s the Difference?
|Parameter||NMI Standard||Compendial Standard||Certified Reference|
|Reference Material||Analytical Standard||Research Chemical|
|Type||Primary Measurement Standard or Primary Standard (Pharma)||Primary or Secondary Standard|
Understanding your reference material certificate of analysis
With the Certified Reference Material (CRM) or Reference Material grade comes the Certificate of Analysis (CoA). Within the CoA, there are several quality parameters which are critical to understand: accuracy, consistency, homogeneity, purity, and stability. Also, what is being certified is important to understand – namely, the certified property value, whether a concentration, potency or content.
Be sure to examine the CoA for the producer’s quality systems, the reference material’s certification process, and supporting information on traceability for a CRM. The CoA is important since it can give the laboratory information which ensures the reference material’s certification is fit for purpose within the testing method or application.
Comparison to a primary source or certified second source – curve/calibration standard. Comparison of multiple independent preparations.
Lot-to-lot consistency verified by comparing to the previous lot.
Expiration date established though real-time stability studie.
Across the batch of ampoules/vial.
Consistent with the neat material. No contamination or degradation.
Reference Material Formats – Do you need a neat, solution or matrix material?
Reference materials can be used in different formats in the testing laboratory, depending on product availability and method requirements. The three formats for reference materials are a neat or powder form, in solution, or matrix. The Supelco® family of reference materials includes CRMs, RMs, or Analytical Standards in each format depending on the testing laboratory’s need and testing application.
Table 2. Different Formats – How Reference Materials are Used in the Testing Laboratory
|Neat Analyte||In Solution||In Matrix|
|Uses||Weigh daily/weekly to make|
stock levels & working solutions
|Ready-made, certified and|
ready to use or dilute
|Ready-made and certified at|
working level in matrix of choice
Flexible to use in a
variety of applications
Larger unit sizes available
|Convenient – Saves time|
Concentration is certified
Stable – protected from
evaporation, transpiration, O2
|Convenient – Saves time|
Remove need to further dilute
into matrix of choice
Concentration and stability is
certified and traceable
|Cons||Maybe hard to handle: Hygroscopic, viscous, unstable|
Potentially greater week-week variability in results
|Need correct mix of analytes at right concentration and volumes|
Diluent compatibility with method
|Long-term analyte stability|
in matrix vs. diluent
Special handling considerations & storage of biological matrices
Choose the correct reference material for your testing purpose
For instrument qualifications and calibrations, establishing and maintaining traceability is critical. The selected reference material should help the laboratory achieve this. In daily routine system suitability applications, it might be important to qualify something that is practical and easy to use, yet reliable and cost effective for everyday use. In method validation, it’s critical to use highly accurate and precise materials to show that the laboratory method is accurate and precise. For identity and screening purposes, important attributes of reference materials include proven authenticity and identity. For quantitation, assays, or stability assessment, stable and accurate reference materials are needed.
Table 3. Use of Reference Materials – Type of Test
|Type of test||Use of Reference Material||Examples||Requirements of the Reference Material|
|Establish system performance|
Routine balance calibrations
|Daily / weekly|
System / method specific
Establish routine performance
|Pre-use Balance calibrations|
System performance checks for
|Qualify as suitable|
Specificity & interferences
LOD/LOQ & Linearity
|Pharma QC; Environmental testing|
Standards of the analyte(s), interferences, impurities
|Identity||Comparison of unknown to known||In-coming raw materials in|
pharma, food etc.
|Content or assay||Quantitation of analytes||Pesticide/toxin limits|
Pharma QC – API content
|Stability assessment||Monitor product stability||Pharma QC||Stable, homogenous|
|Internal Quality Control||Method accuracy||Routine quantitation of analytes|
Which quality grade is the best fit for purpose?
Fit for purpose decisions in selection of reference materials can depend on several factors, from regulatory requirements, availability, and type of testing application to level of accuracy and sample matrix.
Table 4. Fit for Purpose Guidance in Standard Selection
|Type of Test||NMI Standard||Compendial Standard||Certified Reference|
|Analytical Standard||Reagent Chemical||Attribute|
|Method validation||✔||✔||✔||✓||Accuracy, Precision,|
|Content or assay||✓||✔||✔||✔||maybe||Qualified standard|
To learn more about the Supelco® family of reference materials please visit the website here.