技術資料

Making Sense of the Data: Qualitative versus Quantitative

18 Feb 2026

I have been involved in several conversations recently where the terms “qualitative” and “quantitative” have been used incorrectly when discussing data. Let’s take some time to go over the definitions of both terms and discuss when it is appropriate to use each term. Analytical data processing is typically broken into two unique categories: qualitative and quantitative. These two terms can often be confused but fundamentally they are different approaches that can have significant implications in accurate data reporting.

So, what is the difference, why does it matter, and when should we use them? To dive into this, some definitions will be defined below:

Qualitative data [1]:
Data representing information and concepts that are not represented by numbers.

Quantitative data [2]:
Data represented numerically including anything that can be counted, measured, or given a numerical value.

Accuracy [3]:
Degree of conformity of a measure to a standard or true value.

Precision [4]:
How well measurements agree with each other across multiple tests.

Graphical Representation of Accuracy and Precision [3,4]

Accuracy and Precision

Mean [5]:
The total sum of values in a sample divided by the number of values in your sample.

Standard deviation (SD or σ) [6]:
A measure of how dispersed the data is in relation to the mean.

Percent relative standard deviation (%RSD) [7]:
The standard deviation expressed as a fraction of the mean and reported as
a percentage of the mean (%RSD) aka coefficient of variation.

Let’s look at an example using a cannabinoid data set. This experiment monitored 16 cannabinoids in cannabis flower over three distinct injections. The data was processed via instrument software and the mean, standard deviation, and % RSD were subsequently tabulated in Excel. Results can be found in Table 1.

Table 1: Data Collected for 16 Monitored Cannabinoids Where ND Is Non-Detectable

AnalyteInjection 1Injection 2Injection 3MeanSD% RSD
RtAreaRtAreaRtAreaRtAreaRtAreaRtArea
CBDVANDNDNDNDNDNDNDNDNDNDNDND
CBDVNDNDNDNDNDNDNDNDNDNDNDND
CBDA2.01130042.00130062.01130692.00130260.0036.960.100.28
CBGA2.086248632.096231802.096258972.096246470.001371.360.100.22
CBG2.21223282.21222092.21221912.21222430.0074.450.110.33
CBD2.34146862.34144362.36145942.34145720.00126.440.090.87
THCVNDNDNDNDNDNDNDNDNDNDNDND
THCVANDNDNDNDNDNDNDNDNDNDNDND
CBN3.3413113.3417303.3519743.3516720.01335.330.1820.06
CBNANDNDNDNDNDNDNDNDNDNDNDND
Δ9-THCNDNDNDNDNDNDNDNDNDNDNDND
Δ8-THCNDNDNDNDNDNDNDNDNDNDNDND
CBLNDNDNDNDNDNDNDNDNDNDNDND
CBC5.07162845.07771945.08467825.07767530.01455.680.136.75
THCA-ANDNDNDNDNDNDNDNDNDNDNDND
CBCANDNDNDNDNDNDNDNDNDNDNDND

There are different ways to make these calculations. If making the calculations by hand, the following formulas should be followed:

image 5
image 6
image 7

An alternative approach to these calculations is using an application like Excel. In an ideal situation, acceptable standard deviation and %RSD values often vary by industry and method. For cannabis/hemp analysis, an acceptable %RSD is between 10-20% [6-8], depending on the state regulations. For this example, we are going to assume the average at 15% RSD. As mentioned above, a total of 16 cannabinoids were monitored, six were detectable.

Because of the inconsistencies in response from injection to injection and the elevated %RSD value, CBN can only be reported as qualitative. This can be typical for CBN as it is a degradation product (minor cannabinoid) of Δ9- THC rather than a primary cannabinoid.

The five additional detectable cannabinoids demonstrate %RSD values ≤7%, indicating reproducible accurate data from injection to injection, and ensuring valid quantitation of data.

When processing data for means of reporting, it is important to differentiate if it is qualitative or quantitative. These two reporting mechanisms vary depending on the work being performed and, in some instances, one method be more relevant than the other. Statistical analysis like standard deviation and %RSD can help ensure that the method is working appropriately and the data is precise when performing quantitative analysis. These calculations will help indicate which analytes should only be reported as qualitative or quantitative when method reporting is required.

References:

  1. NIH, National Library of Medicine, Qualitative Data, (2022). https://www.nnlm.gov/guides/data-glossary/qualitative-data#:~:text=Definition,Relevant%20Literature  
  2. NIH, National Library of Medicine, Quantitative data, (2022). https://www.nnlm.gov/guides/data-glossary/quantitative-data
  3. Merriam-Webster.com, Accuracy, (2026). https://www.merriam-webster.com/dictionary/accuracy
  4. MedCalc, MedCalc Manual, Accuracy and precision, (2026) https://www.medcalc.org/en/manual/accuracy-precision.php  Accessed August 24, 2025.
  5. M. Hurley, S. Tenny, NIH, National Library of Medicine, Mean, StatPearls Publishing, (2025) https://www.ncbi.nlm.nih.gov/books/NBK546702/
  6. NIH, National Library of Medicine, Finding and using health statistics, Common terms and equations: Standard deviation,  https://www.nlm.nih.gov/oet/ed/stats/02-900.html  Accessed August 24, 2025.
  7. G. Christian, P. Dasgupta, K. Shug, Analytical Chemistry, Seventh edition, John Wiley & Sons (2014) 74. https://kvmwai.edu.in/upload/StudyMaterial/Analytical-Chemistry-by-Gary-D_-Christian-Purnendu-K_-Dasgupta-Kevin-A_-Schug-z-lib_org_.pdf
  8. Calculator.net, Math: Standard Deviation Calculator. https://www.calculator.net/standard-deviation-calculator.html  Accessed August 24, 2025
  9. New Jersey Cannabis Regulatory Commission, Testing guidance, revision 2.0 (February 6, 2025). https://www.nj.gov/cannabis/documents/businesses/Business%20Resources/NJ-CRC_Testing_Guidance_2-19-25.pdf

Author

  • Melinda Ulrich

    Melinda “Mel” Urich is an applications scientist in the LC Solutions department. Her primary focus is on the development of novel applications in the cannabis and food markets. In her previous role at Restek as an LC manufacturing chemist, she led the synthesis of silica, bonding of stationary phases as well as new process implementations and improvements. Mel attended Juniata College where she earned her BS in Chemistry and performed research in Atomic Force Microscopy AFM).

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