---
title: "Temperature Mapping: Ensure Quality & Compliance | Dickson"
description: This guide from Dickson describes the key concepts of temperature mapping and the areas where it can be used, helping your organization ensure product quality is protected and compliance is maintained.
---

[Dickson Resource Blog](https://info.dicksondata.com/blog)

# [Temperature Mapping: Ensure Quality & Compliance | Dickson](https://info.dicksondata.com/blog/temperature-mapping-quality-compliance)

 Written by [Antoine N](https://info.dicksondata.com/blog/author/antoine-n) | May 19, 2020 10:04:13 PM

In regulated industries, we often encounter materials and processes that are highly sensitive to temperature and humidity. The storage of certain pharmaceuticals is one example. In these situations, temperature mapping, also referred to as thermal mapping, is a GxP method that is used to prevent the impact of temperature or humidity fluctuations to product quality. (Note that in this context, “thermal mapping” collectively refers to both temperature and humidity.) 

As its name suggests, temperature mapping involves meticulous, three dimensional mapping of a controlled space, and can be done on the scale of individual process chambers like ovens or freezers, warehouses, or even [across distribution and supply networks](http://intelsius.com/wp-content/uploads/2011/10/Pharma-Cold-Chain-Bishara_APR.pdf). In the context of GxP, temperature mapping is a way to validate and document that [a temperature-controlled space is suitable](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_7.pdf?ua=1) for its purpose.  

Temperature *mapping* should not be confused with the continuous temperature *monitoring* that would be a customary part of manufacturing, storage, and distribution of sensitive products. In temperature mapping, many data loggers are placed throughout the region of interest, more than would be used for typical monitoring, in order to develop a comprehensive picture of the conditions inside a space. 

Mapping is done over a representative period of time, across a range of operating conditions (for example, with the space empty and loaded to capacity, as well as stress conditions like during door opening or power outages). The results of a mapping exercise can then be used to make a [plan for routine monitoring](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_6.pdf?ua=1), to recommend remedial action, or to develop an SOP for the arrangement of products in the space. 

As with other [GxP methods](https://info.dicksondata.com/blog/an-essential-guide-to-gxp-good-practices-for-heavily-regulated-industries), temperature mapping is used in heavily regulated industries, including:

- Pharmaceutical and biotech manufacturing and testing
- Medical device manufacturing
- Laboratory operations
- Food and Beverages
- Warehousing, distribution, transportation, and other logistics involved with these industries

## Why Temperature and Humidity Mapping Are Important

Accurate and thorough thermal mapping is important for a number of reasons, including:

- **Safeguarding your products, consumers, and your finances.** This is the primary goal, particularly in the case of drug or food storage. The results of a mapping study can be combined with knowledge of the [effects of ](https://pharmacy.ks.gov/docs/default-source/default-document-library/ups-36-good-storage-and-shipping-practices.pdf)[temperature and humidity](https://pharmacy.ks.gov/docs/default-source/default-document-library/ups-36-good-storage-and-shipping-practices.pdf) on product effectiveness, safety, and overall quality to implement systems to prevent these products from experiencing harmful excursions. 

- **Maintaining regulatory compliance.** In the U.S., the FDA regulates the safe handling and storage of foods, tissue and blood samples, pharmaceuticals, medical devices, and the components used to make them, through various parts of [Title 21 of the CFR](https://www.ecfr.gov/cgi-bin/text-idx?SID=85d5a1b2cfd68a86a25eb474688e1bc2&mc=true&tpl=/ecfrbrowse/Title21/21tab_02.tpl). This includes regulations for temperature and humidity control.

- - For example, 21 CFR 211.142 states that drug products should be stored under “appropriate conditions of temperature, humidity, and light so that the identity, strength, quality, and purity of the drug products are not affected”. Regulations for food products and human tissues and cells can be found in 21 CFR 110.80 and 21 CFR 1271.60, respectively. 

- - [FDA inspection citations](https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/inspection-references/inspection-citation) from the last 10 years contain many instances of temperature and humidity control problems, mainly for foods, pharmaceuticals, and human tissue storage.

- - Part of ensuring that these and other similar regulations are followed, and preventing regulatory action, is having a documented temperature mapping process, as well as evidence that the results of the mapping process are used to guide monitoring and control. 

-  
- **Understanding the performance and capability of the HVAC systems**. A thorough mapping study will determine whether the existing HVAC configuration can adequately control conditions in the space. Mapping includes stress testing the system at the extremes of conditions likely to be encountered, including loading, outside temperature and humidity variations, door opening, and power failures. 

- **Developing a data-based foundation for determining your monitoring needs in the future.** This reduces cost and improves overall productivity, by allowing the implementation of [efficient monitoring solutions](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_6.pdf?ua=1) that require minimal manual intervention. Having a complete understanding of the response of your temperature control systems under non-standard conditions also helps to reduce disruption when issues arise. 

The importance of thermal mapping is demonstrated by the number of organizations that have published detailed guidelines, including [the WHO](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_8.pdf?ua=1), [ISPE](https://ispe.org/publications/guidance-documents/good-practice-guide-controlled-temperature-chamber-mapping-monitoring), [USP](https://pharmacy.ks.gov/docs/default-source/default-document-library/ups-36-good-storage-and-shipping-practices.pdf), and [PDA](https://www.pda.org/bookstore/product-detail/4382-tr-64-active-temperature-controlled-systems), among others. 

## Areas Where Mapping Is Critical

There are a number of specific areas where temperature mapping can be applied. Some of the most common include:

- **Warehouses**. Temperature mapping should be considered part of the [OQ and PQ steps](https://info.dicksondata.com/blog/iq-oq-pq-how-to-navigate-essential-quality-assurance-processes) (operational qualification and performance qualification) when commissioning a new warehouse or storage area. 
  
  An example is the temperature mapping of a warehouse that is intended to store pharmaceuticals within a safe storage temperature window, based on prior stability studies, labeling, or recommendations from the manufacturer. The process would involve simultaneous measurements of temperature and humidity at many points within the 3 dimensional space of the warehouse, over a representative time period (usually a few days to a week). Measurement points are carefully selected to identify hot or cold spots, as well as to find trends, for example temperature variation horizontally or vertically across storage racks. Data would also be collected around potential problem areas, like heating/cooling vents, doorways, and skylights, and other critical points around data loggers used for feedback to the HVAC system. 
  
  Data from the mapping study data could then be used to identify areas where remedial action needs to be taken, or where products should not be stored. Any hot or cold spots identified in the mapping study could be used as [locations for routine temperature monitoring](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_6.pdf?ua=1) going forward.

- **Refrigerators, freezers, and cold rooms**. For example, a refrigerator for the storage of time and temperature sensitive pharmaceutical products (TTSPPs). In this case, a mapping study would [indicate areas of the refrigerator that would be unsafe](https://www.who.int/medicines/areas/quality_safety/quality_assurance/TS-mapping-storage-areas-final-sign-off-a.pdf) for storage due to proximity to cooling coils or fans, or where to place temperature probes for feedback to temperature alarms. 
- **Transportation equipment**. Dedicated shipping containers or other transport vehicles can be [mapped in a similar way as a warehouse or cold room](https://www.who.int/medicines/areas/quality_safety/quality_assurance/TS-reefer-qual-final-sign-off-d.pdf). For non-dedicated transport, like a mail truck, another option is to use insulated packaging that has itself been [qualified using a mapping procedure](https://pharmacy.ks.gov/docs/default-source/default-document-library/ups-36-good-storage-and-shipping-practices.pdf) that simulates the shipping process. For refrigerated products, temperature mapping of warehouses and shipping containers can be integrated to [map the full “cold chain” of distribution](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821242/).
- **Processing areas**. It is important that other areas where temperature-sensitive products could be stored are also mapped. Examples of these include manufacturing areas, packing and labeling areas, and loading docks.
- **Stability chambers**. Among other things, stability chambers (chambers with precisely controlled temperature, humidity, and other conditions) can be used for studies to determine the stability of drugs and drug packaging over time. Because the results of these studies will be used to make decisions about shelf stability and safe storage- and often later combined with temperature mapping of storage units- it is particularly important that these chambers be accurately mapped, understood, and monitored. 
- **Ultra-low temperature freezers**. These freezers, which store samples at temperatures as low as -90 °C, are used to store human tissue, cells, and biologics. Due to the extreme sensitivity of the materials stored in them, the College of American Pathologists (CAP) requires [temperature mapping of these freezers](http://elss.cap.org/elss/ShowProperty?nodePath=/UCMCON/Contribution%20Folders/DctmContent/education/OnlineCourseContent/2017/LAP-TLTM/checklists/cl-bap.pdf) as part of their lab accreditation program. In this case, [particular attention should be paid](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479232/) to the arrangement of samples inside the freezer, and the effect of opening the freezer door. 
- **Sterilizing equipment**, for example, [autoclaves used in aseptic processing](https://www.fda.gov/media/71026/download), should be qualified using thermal mapping to ensure adequate temperature uniformity and sufficient lethal temperatures are reached during sterilization cycles. This will ensure that manufacturing parts and packaging materials (e.g. rubber stoppers, caps) are adequately sterilized prior to use in an aseptic environment.
- **Ovens**. Temperature mapping can be used for ovens at a range of scale, from small lab units to production scale, across various industries, including drug manufacturing and industrial scale food preparation. Ovens could be temperature mapped as part of a pre-shipment check, or mapped again after installation.
  
  An example of a mapping exercise in an oven would be to measure the temperature at several points inside the oven, in the corners and the center, for example, at different setpoint temperatures.
- **Incubators**. Incubators, and ovens to some extent, can involve a different aspect of mapping. In addition to storage at constant temperature, they involve heating a material up from ambient temperature. For storage, variation in air temperature typically represents the worst case scenario for variability, since it will change more quickly than the temperature of the product being stored. However, in incubators, where the temperature of the medium can be dynamic, it may be necessary to place temperature data loggers in the medium, in addition to measuring the temperature in the air space.

## 8 Steps to Getting Thermal Mapping Right

- **Develop a test plan**

- - The plan should lay out the number and position of the temperature and humidity data loggers in three dimensions, based on a [site survey](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_8.pdf?ua=1). 
    - The main objective of placement is to characterize the variation across the entire storage space, and to be able to detect spatial trends. 
    - Considerations for data logger placement include:  
          - Dimensions of the space, and how much of the space is usable for product placement
          - Storage arrangement like shelves, racking, and pallet stacking
          - Location of active heating or cooling components
          - Location of doors (internal and external) and skylights
          - Possible temperature stratification over height in areas with high storage, such as mezzanines
          - Any other sources of temperature nonuniformity.
    - The plan should include [mapping the space under empty and loaded conditions](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_7.pdf?ua=1) (OQ and PQ). Cyclical processes should also be considered, like shift changes or weekday versus weekend operations.

- - However, the test plan should not only contain information on how to execute the measurements. A comprehensive plan also includes: 
          1. Objectives of the mapping study. This section will drive decisions made in other parts of the study. For example, the decision of whether or not humidity measurements are performed in a warehouse could be based on a previous study of the effect of humidity on product stability. 
          2. Description of the[type of temperature and humidity measurement equipment](http://www.uspbpep.com/usp31/v31261/usp31nf26s1_c1118.asp) that will be used. This equipment is selected based on factors like accuracy, response time, material compatibility, memory capacity, and measurement range. Temperature measurement could be done by self-contained loggers that measure, record, and store temperatures, or by remote data loggers that send data back to a central recording device. Note that for FDA-regulated operations, software should be compliant with [21 CFR Part 11](https://www.fda.gov/regulatory-information/search-fda-guidance-documents/part-11-electronic-records-electronic-signatures-scope-and-application). 
          3. Rationale for selecting data logger placement, type, monitoring time, and other parameters of the study
          4. Summary of the site survey
          5. Acceptance criteria for temperature and humidity ranges, if applicable. For warehouse storage, this could be based on the known effects of temperature and/or humidity on stability. For ovens and sterilization equipment, it could be based on specifications of the process in which the equipment is used. 
          6. Listing of IDs and serial numbers of individual data loggers and their location
          7. Template for the final report (this is particularly helpful if the same test plan will be used for multiple spaces)
          8. List of members of the mapping team, and a record of approvals and  modifications to the plan

- **Calibrate and program sensors and data loggers**

- **Place measurement equipment and execute measurements in test plan**

- **Retrieve measurement equipment**

- **Download and analyze data**

- **Post-calibrate measurement equipment**

- **Complete mapping report**

- **Make Recommendations**

These steps, with appropriate modifications, can be used across many different temperature controlled spaces. 

It is recommended to repeat mapping periodically, or after significant changes to the space or the temperature control system. For spaces that are sensitive to seasonal variation in temperature and humidity, it may also be necessary to [repeat mapping at different times of the year](https://www.who.int/medicines/areas/quality_safety/quality_assurance/supplement_7.pdf?ua=1) to represent the extremes of outdoor temperature variation. Note that while climate data is useful in determining where mapping is needed, it is not a substitute for mapping.

## Should you bring in outside expertise for a thermal mapping project?

There are three main reasons for calling on outside experts for help with thermal mapping projects. The first is cost. Thermal mapping generally requires specialized equipment and software, and the use of many more temperature monitors than would normally be used during routine operations. For most companies, this equipment would have a very low utilization rate if mapping was performed in-house. In addition, outside experts can handle calibration and maintenance of the measuring equipment, avoiding the need for third-party calibration. 

The second reason is that most companies do not have the required expertise on staff to plan, execute, and interpret the results of a thermal mapping project. As with many aspects of GxP, these projects are highly detail-oriented and require rigorous documentation. 

The complexities of the mapping process leads to a third reason organizations often seek outside help: time. Because of the detailed nature of the work, a typical mapping project can require 130-250 person-hours. The best way to ensure the creation of sound test plans that generate high quality reports and data-based recommendations is to rely on experts who routinely perform this work. This also minimizes the likelihood of mistakes during mapping, which can result in costly fixes or regulatory actions later on. 

## Conclusion

Thermal mapping is a detail-oriented, rigorous process that should be part of the qualification of any new temperature-controlled chamber or storage space. Correctly working through the mapping process will lead to a more efficient temperature control and monitoring scheme, less downtime and product loss due to excursions, and ultimately contribute to an overall GxP environment that ensures product quality and regulatory compliance.

Questions about thermal mapping or other environmental monitoring needs? [Contact Dickson](https://dicksondata.com/resources/contact/) today. 

 

*About the author: Before coming to Dickson, Director of Services Antoine Nguyen spent more than 18 years in quality and validation roles in the pharmaceutical and medical device industries.*

[View full post](https://info.dicksondata.com/blog/temperature-mapping-quality-compliance)

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