3 Types of Human Error and Potential CAPAs to Prevent Them

Human performance plays a crucial role in all aspects of our lives, ranging from everyday tasks to complex professional endeavors. However, even the most skilled individuals are prone to making errors. Understanding the different types of errors and implementing corrective actions can significantly enhance performance and minimize mistakes. In this blog post, we will delve into the three main types of errors: slips, lapses, and mistakes, and explore effective strategies to address each of them.

As we examine the intricacies of human performance and the different types of errors, it becomes clear that a comprehensive approach is required to unlock our full potential. Thankfully, the cognitive scientist Jens Rasmussen's did this for us with his SRK (Skills Based, Rule Based, and Knowledge Based) model. The SRK model offers valuable insights into the underlying mechanisms of human performance and how errors manifest in various contexts. Rasmussen's work emphasized that as individuals acquire expertise in a particular domain, their actions progress through three levels: skills-based, rule-based, and knowledge-based. Slips and lapses primarily occur at the skills-based level, where automated and habitual actions take place. These errors often arise due to momentary distractions or deviations from established routines. Think of being on autopilot. Mistakes, on the other hand, are more likely to occur at the rule-based and knowledge-based levels. They involve conscious decision-making and may stem from faulty assumptions, inadequate knowledge, or flawed reasoning. In these levels, individuals are integrating, interpreting, and applying what they’ve learned or experienced. By incorporating Rasmussen's insights into the SRK model, you can gain a deeper understanding of the cognitive processes underlying slips, lapses, and mistakes. This awareness enables you to tailor CAPAs accordingly, fostering a holistic approach to error prevention and performance improvement.

  1. Slips: Slips are unintentional actions that result in an unintended outcome. The keyword here is “unintentional.” We have to remember that people do not go to work thinking, “today I am going to mess up!” Slips typically occur when a person's performance deviates from their intentions due to a momentary lapse inattention or an automatic response. Slips can be categorized as motor or cognitive slips. For example:

    - A QC technician accidentally selects the wrong reagent or solution due to similar labeling or packaging,
    - Or transfers an incorrect volume of a substance during a pipetting process due to momentary distraction,
    - An operator mishandles a piece of equipment, leading to unintended contamination or spills.

    a. Potential CAPAs:

    i. Increase awareness: Being mindful of one's actions and maintaining focus can reduce the occurrence of slips. Taking a moment to pause, breathe, and concentrate on the task at hand helps prevent distractions. A great tool here is the STAR tool: Stop, Think, Act, Review
    ii. b) Implement reminders and checklists: Utilizing reminders, checklists, or visual cues can help individuals stay on track and avoid slipping into automatic modes of behavior. These aids serve as external prompts and keep important details at the forefront of one's mind.
    iii. c) Improve ergonomics and design: Optimizing the environment and workflow can minimize slips. Simple modifications such as arranging tools and equipment for easy access, reducing clutter, and designing intuitive interfaces can enhance performance and reduce the likelihood of errors.
  2. Lapses: Lapses are errors of omission, where an individual forgets to perform a necessary action or fails to complete a task. They often occur due to a lack of attention, memory failure, or absent-mindedness. For example:

    - An operator forgets to document a critical step or measurement,
    - Or neglects to open their SOP because they’ve done the task a million times and skips a necessary quality control check,
    - A QA release technician overlooks the expiration date of a crucial reagent or material, leading to the release of outdated components.

    Like slips, lapses occur during actions that require little conscious control. Typically, individuals who experience slips and lapses are extremely experienced with the task and because of this, re-training is never the answer..

    a. Potential CAPAs

    i. Utilize reminders and alarms: Employing technology, such as setting reminders on smartphones or using alarm systems, can help counteract memory lapses. These tools provide timely prompts and ensure critical tasks are not overlooked.
    ii. Establish routines: Establishing consistent routines and habits helps minimize lapses by transforming important actions into automatic behaviors. By performing tasks regularly at specific times or following a predetermined sequence, individual scan reduce the risk of omission. GDP errors often are the result of a slip or lapse, so establishing real-time or frequent document review during a shift will help with recognition of these errors.
    iii. Enhance working memory: Techniques such as mnemonic devices, visualization, and association can aid in remembering important information. Breaking complex tasks into smaller, manageable chunks and actively rehearsing key details can improve memory retention.
  3. Mistakes: Mistakes differ from slips and lapses as they involve a conscious decision-making process that leads to an incorrect or undesirable outcome. Mistakes often arise due to flawed reasoning, incorrect assumptions, or inadequate knowledge. When individuals make a mistake, there is almost always some form of problem solving that needs to occur. They typically thought they were doing what they were supposed to, but their planning was flawed. Any shortcomings in an individual’s knowledge or their limitations in applying existing knowledge to new situations will be evident. For example:

    - An operator misinterprets the data analysis results and makes decisions based on flawed interpretations, leading to incorrect adjustments in manufacturing processes,  
    - Engineering qualifies a bioreactor with incorrect specifications, resulting in suboptimal growth conditions for the cells or microorganisms,
    - Quality and Manufacturing management fail to adequately assess potential risks associated with a new manufacturing processor technology, leading to unforeseen safety or quality issues.

    a. Potential CAPAs

    i. Continuous learning and training: To reduce mistakes, individuals must invest in ongoing learning and professional development. Expanding knowledge, staying updated on relevant information, and seeking feedback from peers or mentors can enhance decision-making abilities.
    ii. Encourage a culture of double-checking: Instilling a habit of verifying one's work and seeking second opinions can catch potential mistakes before they cause significant harm. This practice fosters a collective responsibility for quality assurance and encourages critical thinking.
    iii. Foster open communication: Creating an environment where individuals feel comfortable discussing concerns and asking questions is crucial. Encouraging open dialogue and promoting a blame-free culture fosters collaborative problem-solving and minimizes the likelihood of mistakes going unnoticed. After action reviews are an amazing tool used by the military and many other high-risk industries, where an open dialogue between team members can help uncover what was supposed to happen, what actually occurred, what went well and why, and where improvement scan be made.

Understanding the various types of errors and implementing corrective actions is essential for optimizing human performance. By recognizing slips, lapses, and mistakes, individuals can take proactive measures to mitigate their impact. Cultivating mindfulness, utilizing reminders, establishing routines, continuously learning, and fostering open communication are key strategies to enhance performance and reduce errors. By incorporating these practices in to our daily lives, we can strive for excellence in our personal and professional endeavors.


Sarah Boynton, a Consultant on the Quality Executive Partners team, has extensive experience in the biopharmaceutical/cell and gene therapy space, with a particular focus on cGMP training, human performance/error prevention, downstream processing, and non-conformance investigations. Prior to joining QxP, Sarah worked for Catalent Pharma Solutions, KBI Biopharma, AstraZeneca, MedImmune, and GlaxoSmithKline.

Check out Sarah’s other recent blog: “The 5 Questions You Need to Ask After a Human Error Event Occurs.”

Pharmaceutical Industry Trends for 2024 So Far

Christine Feaster
April 24, 2024

Decoding the Technical Transfer Process in Biotech Manufacturing

Sarah Boynton
April 23, 2024

Quality Executive Partners - IACET Accreditation

Ken Mead
April 9, 2024

Coaching and Correcting: A Focus on Behavior Over Blame

Sarah Boynton
November 1, 2023

The Importance of Roles and Responsibilities in Biotech Manufacturing & Human Error Prevention

Sarah Boynton
October 26, 2023

Remote cGMP Inspections and AI in Drug Manufacturing

Michelle Fishburne
October 11, 2023

4 Best Practices for Effective Investigation into Deviations

Sarah Boynton
September 19, 2023

The Art of Viral Vector Manufacturing: 4 Essential Controls to Prevent Cross-Contamination

Sarah Boynton
September 13, 2023

Practicing Risk Acceptance

Mark Roache
August 28, 2023

Annex 1 – Can we all take a deep breath now?

Vanessa Figueroa
August 24, 2023

In Cell and Gene, Good Science is Necessary, But Not Sufficient

Mark Roache
August 21, 2023

6 Ways To Achieve Manufacturing Audit And Inspection Readiness

Sarah Boynton
August 14, 2023

Experience is What You Get Just After You Needed It, Part 2

Mark Roache
August 10, 2023

Experience is What You Get Just After You Needed It, Part 1

Mark Roache
August 10, 2023

Sterility Assurance Matters to This ONE

Greg Gibb
August 8, 2023

Enhancing Quality and Safety: 3 Essential Human Error Prevention Tools for cGMP Manufacturing

Sarah Boynton
August 3, 2023

Asia-Pacific Happenings: Samsung Bioepis Implements QxP Virtuosi®

Michelle Fishburne
August 2, 2023

CDMOs – Selecting the Right One for Each Manufacturing Stage

Christine Feaster
July 24, 2023

Drug Shortages: Causes & Solutions

Christine Feaster
July 10, 2023

The 5 Questions You Need to Ask After a Human Error Event Occurs

Sarah Boynton
July 5, 2023

Understanding How Adults Learn

Mike Levitt
June 30, 2023

Annex 1 and Ensuring Filling Technologies Fit the Need

Natasha Howard
June 21, 2023

How to Solve Pharma’s Skilled Workforce Deficit

Jeff Roy
June 20, 2023

ChatGPT Told Me AI is “Imperative” in Pharma Manufacturing

No items found.
June 18, 2023

Get Ready: FDORA’s Unannounced Foreign Inspection Pilot Program is On!

Crystal Mersh
June 6, 2023

Nitrosamines Impurity Challenges

Christine Feaster
June 2, 2023

All You Need to Know About Contamination Control Strategies, Parts 1 and 2

No items found.
June 1, 2023

When is ISO 8 Not ISO 8?

Bob Ferer
May 30, 2023

Cost Of Quality: Worth Every Cent In Bio/Pharmaceutical Manufacturing

Crystal Mersh
May 24, 2023

Pharmaceutical Quality is NOT a Spectator Sport

Mike Levitt
May 22, 2023

The Six Keys for Effective Deviation Investigators

Mike Levitt
May 18, 2023

There Has to be a Better Way to Train

Tyler DeWitt, Ph.D.
May 15, 2023

Cell and Gene: Article Series on CGT’s Key Drivers

Mark Roache
May 8, 2023

Bacterial Endotoxin Testing is on the Move

Christine Feaster
May 5, 2023

Top 20 Pharma Company Chooses QxP Virtuosi® Platform

Vanessa Figueroa
May 3, 2023

Crystal Clear: Controls Are Not Enough

Crystal Mersh
April 22, 2023

Myth #1: Complying with Regulations and Product Specifications

Brian Duncan
April 20, 2023

Myth #2: Proactively Remediating Bad Inspection Outcomes: What’s the benefit?

Brian Duncan
April 20, 2023

Is it Time to Outsource Internal Auditing?

Mike Levitt
April 18, 2023

Quality is Number One, Even When Trying to Address Supply Chain Issues

Christine Feaster
April 14, 2023

Don’t Be a Daredevil When Retrofitting Your Facility, Part 2

Bob Ferer
April 10, 2023

Don’t Be a Daredevil When Retrofitting Your Facility, Part 1

Bob Ferer
April 10, 2023