Skip to main content Skip to search Skip to main navigation

Deviation Causes as KPIs – Collection vs. Assessment

7 min. reading time | by Felix Kern, PhD and Liwa Schneider
Published in LOGFILE 11/2022

Deviation management plays an increasingly important role in the collection and review of KPIs (Key Performance Indicators) for pharmaceutical production and quality processes. Tracking the cause of deviations in particular provides information on how stable the respective processes are, where there are gaps and where countermeasures need to be taken with corrective and preventive actions (CAPAs).

However, difficulties can arise depending on how these indicators are collected.

In general, there is a wide variety of different causes for deviations. Classic examples are:

  • Environmental conditions: A storm damages the ventilation system for a production plant.
  • Machine: A tabletting stamp breaks due to motor damage.
  • Human Error: An employee forgets to carry out an in-process control due to carelessness.
  • Material: During the incoming goods control, glass particles are found in a raw material.
  • Method: A manufacturing instruction is formulated too imprecisely and left room for interpretation or was not understood by the staff.
    The manufacturing instruction specifies work steps in an illogical order.
  • Data Integrity: A system crash with loss of raw data occurs during measurement in a laboratory.

The KPI ‘human error‘ in particular is gaining in importance and is increasingly being assigned upper limits in the performance targets. A high human error rate can indicate many things. This could be, for example:

  1. A superficial deviation handling. In many cases it is easier to attribute the cause of a deviation to an employee error than to spend time researching what is really behind the error. This could be, for example, training deficits, specification deficits or system deficits.
  2. A systematic staff problem. This can be multi-tasking, for example, which means that staff members perform too many tasks in parallel: A staff member takes care of the operation of two devices at the same time: the visual inspection of units at defined time periods and the cleaning of surfaces.
  3. There is an actual human error. This could be, for example, the deliberate contravention of an instruction or a lack of concentration.

However, attention must also be paid to how the human error rate is collected. Absolute or relative values are possible here. For absolute values, this means that out of 100 deviations, 20 deviations are caused by ‘human error‘. The relative value would be 20%. For tracking, the absolute value is more suitable than the relative value. Why is this so? The following is an example:

Let's assume that out of 100 deviations, we have 50 with the cause ‘human error‘ and 50 with the cause ‘machine‘. Now the target (relative value) for the KPI human error is set at 20% and a project is launched to reduce the human error rate. At the same time, a project is started to stabilise the manufacturing processes.

Through the human error reduction project, the absolute value of deviations with this cause is reduced from 50 to 30. This is huge progress. At the same time, by establishing modern machines and modern processes to protect these machines, the number of deviations with the cause ‘machine‘ is reduced from 50 to 10.

Of 40 remaining deviations, 30 fall into the cause category ‘human error‘, which corresponds to an increased relative value of 75%. This means that despite a respectable reduction in the number of deviations with the cause ‘human error‘ from 50 to 30 deviations (absolute value), the relative value has increased from 50% to 75% (cf. Table 1).

Table 1

However, this only considers the case of a constant production volume. If the production volume increases, for example from 100 to 200 batches, it can be assumed that the absolute value of deviations will also increase. This must then also be taken into account when specifying the KPIs as absolute values.


Summary:

Tracking the cause categories of deviations is becoming increasingly important in the KPIs. The focus here is particularly on the cause ‘human error‘. It makes more sense to track this KPI according to the absolute value than according to the relative value, as we have illustrated in the example. In order to interpret these figures correctly and derive meaningful measures from them, one must consider in advance which factors need to be taken into account for correct collection. This is how the KPIs can be properly evaluated.


Do you have any questions or suggestions? Please contact us at: redaktion@gmp-verlag.de

Dr. Felix Kern
Dr. Felix Kern

You may also be interested in the following articles:

Swissmedic Updates Guidance on GMP Compliance of Foreign Manufacturers

Swissmedic Updates Guidance on GMP Compliance of Foreign Manufacturers

Swissmedic has revised its guidance document “GMP compliance by foreign manufacturers”. The new Version 7.0 has been valid since 7 September 2026. In particular, it introduces new provisions for demonstrating the GMP compliance of manufacturers inspected by the US FDA. 
Read more
Swissmedic Updates Requirements for Cooperation with Pre-Wholesalers

Swissmedic Updates Requirements for Cooperation with Pre-Wholesalers

Swissmedic has revised its Technical Interpretation “Market release and distribution in cooperation with a pre-wholesaler”. The document addresses market release and distribution where a Marketing Authorisation Holder works with a pre-wholesaler (logistics and distribution service provider).
Read more
News: Europe

IPEC Updates Two Guides on Pharmaceutical Excipients

The IPEC Federation has updated two key guides on pharmaceutical excipients. The IPEC Composition Guide for Pharmaceutical Excipients (Version 3, 2026) describes an approach for manufacturers to establish excipient composition profiles. The revised version now covers biotechnology- and fermentation-derived excipients, provides further details on component types and physicochemical characterisation, and includes an example composition profile template.
Read more
Applying the FDA’s 7-Step Model for AI/ML Validation in GMP Environments: One Year Later

Applying the FDA’s 7-Step Model for AI/ML Validation in GMP Environments: One Year Later

Artificial intelligence is becoming increasingly important in GMP-regulated environments, presenting companies with new regulatory challenges. This article summarizes the latest regulatory developments, introduces a validation framework based on the FDA's seven-step model, and outlines initial practical experience with AI/ML validation.

Read more
Question of the Week | GMP-Verlag

What are the General Requirements for Standard Documents?

Here's the answer:
Read more
News: Europe

EDQM: Revised Guidance on Sister File Applications

The European Directorate for the Quality of Medicines & HealthCare (EDQM) has revised its Guidance on applications for “sister files” (PA/PH/CEP (09) 141). The revision is intended to support consistent application of the procedure and provide greater clarity on the classification and assessment of the corresponding CEP applications.
Read more
Previous
Next

Related Products

Skip product gallery
GMP Compliance Adviser | Named User Licence | 12M

GMP Compliance Adviser | Named User Licence | 12M

The GMP Compliance Adviser is an online publication that covers all aspects of Good Manufacturing Practice (GMP) in one source.In the GMP Compliance Adviser you’ll find: GMP in Practice This part contains 21 chapters with GMP expert knowledge to base your decisions upon. It provides practical assistance with checklists, templates and SOP examples. It is written by more than 80 authors with hands-on experience directly linked to the industry. The individual chapters describe the different aspects of GMP in clear language. Technical, organizational and procedural aspects are covered.More than 700 checklists, templates and examples of standard operation procedures taken directly out of practice help you in understanding the GMP requirements.GMP RegulationsThese chapters cover the most important GMP regulations from Europe and the United States (CFR and FDA), but also PIC/S, ICH, WHO and many more.  Sample Documents In addition, the GMP Compliance Adviser contains many sample documents and practical examples that you can use.

delivery time appr. 2-5 workdays after receipt of payment
€1,368.00 net excl. VAT
GMP:KnowHow Pharma Logistics (GDP) | Named User Licence | 12M

GMP:KnowHow Pharma Logistics (GDP) | Named User Licence | 12M

Your knowledge portal for GDP-compliant pharmaceutical logistics.  It is important that you as a logistics service provider, but also as a client in the pharmaceutical industry, comply with regulatory requirements. The GMP:KnowHow knowledge portal guides you through the complex regulatory landscape of the pharmaceutical and logistical supply chain! The knowledge portal gives you an easy-to-understand overview of all the important topics. Interactive graphics help you navigate all areas covered by the EU GDP Guidelines (2013/C 343/01). You also have the relevant passages of the regulations directly at hand for each topic. This allows you to compare the requirements directly and saves valuable research time.One thing is certain: the knowledge portal answers your questions about the supply chain of medicinal products, active pharmaceutical ingredients and medical devices. You don't have to be an expert. Yet.You will find answers to your questions in the GMP:KnowHow Pharma Logistics (GDP). Where does GDP begin, where does GMP end? What does GDP-compliant mean? When do I also have to take GMP requirements into account? What permits do I need for certain activities? What requirements do I have to fulfil? What is the current legal basis? How am I covered? What authorizations do I have for my work, e.g. from my employer? Who is responsible — the client or the contractor? And many more What is the difference to the GMP Compliance Adviser? GMP:KnowHow Pharma Logistics (GDP) is a practical knowledge portal dedicated to Good Distribution Practice (GDP). It is a product that is independent of the GMP Compliance Adviser and concentrates on content that is essential for carriers of medicinal products, active pharmaceutical ingredients and medical devices as well as for logistics clients. The focus is on practical knowledge and how to apply it in your daily business. If necessary, the relevant regulations can be called up immediately alongside the practical knowledge, and you can see the relevant paragraphs at a glance. In addition, sample documents are available to help you make immediate progress. AuthorSimone Ferrante, currently Director Quality at Fisher Clinical Services, previously served as Head of Quality Control and Responsible Person (GDP) for the Grieshaber Group. She is also a long-standing author and GDP expert at GMP-Verlag.

delivery time appr. 2-5 workdays after receipt of payment
€610.00 net excl. VAT
E-Learning GMP:READY | Specialist Knowledge GMP for Engineers

E-Learning GMP:READY | Specialist Knowledge GMP for Engineers

Why are GMP rules important for technicians and engineers? Technicians and engineers play a key role in ensuring compliance with Good Manufacturing Practice (GMP) standards. They are involved in critical activities such as: planning and construction of ventilation systems, maintenance of water treatment plants, calibration of measuring sensors. Therefore, they are jointly responsible for the quality of medicines and must ensure that their work complies with GMP standards.Your advantages: Fast familiarization with GMP topics in approx. 2 hours, time- and location-independent online training, printable personal certificate, 12-month access for initial and follow-up training, automatic updates in case of legal changes,content compliant with Article 7(4) of Directive 2003/94/EC.The Author This e-learning course was developed with the collaboration of Dipl.-Ing. Andreas Nuhn (D & B Pharmadesign GmbH).

delivery time appr. 2-5 workdays after receipt of payment
€245.00 net excl. VAT
GMP Fundamentals | A Step-by-Step Guide

GMP Fundamentals | A Step-by-Step Guide

This handbook is a practical and easy to read guideline, giving you a quick and comprehensive overview of the complex world of Good Manufacturing Practice (GMP) without the need of previously acquired knowledge. Some topics are: GMP: Purpose and basic pharmaceutical terms Laws, licenses and inspections Personnel: Responsibility and hygiene Standard Operating Procedures (SOP) and documentation Design of rooms and facilities Processing and packaging Quality control and market release Suppliers, storage and logistics (Good Distribution Practice = GDP) Alphabetical index and abbreviations Using practical examples and comparisons to every-day life will help to easy understand GMP regulations.GMP Fundamentals is a helpful guide which facilitates the entry into the GMP world and teaches the necessary basics.

delivery immediately after receipt of payment
€44.90 net excl. VAT