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The life sciences industry is fast-evolving while leveraging the various uses of artificial intelligence (AI). A recent webinar hosted by ComplianceQuest and led by industry veteran Justin Dear King, co-founder of MyQMS.ai, delivered a compelling case for why AI is transforming Quality Management Systems (QMS) across life sciences and beyond.
AI isn't new. From IBM’s Deep Blue defeating Kasparov in the 90s to Watson winning Jeopardy in 2011, the journey has been long. But it’s only in the last few years that AI has exploded into mainstream applications. Why?
Three core factors have converged:
You may not realize it, but AI is already embedded in your daily life:
Even Medtronic’s implantable cardiac monitor uses machine learning to reduce false positives, proving AI’s validity in patient care and internal systems alike.
AI should augment, not replace, human expertise. Tasks that are repetitive or rules-based are ideal for AI offloading, enabling professionals to focus on innovation, analysis, and decision-making. Instead of spending time proofreading records, researching regulations, or even brainstorming training quizzes, users can leverage the learning capabilities of AI tools like ChatGPT to streamline these repetitive or time consuming tasks with remarkable efficiency.
There is a clear distinction between traditional Machine Learning vs Generative AI:
Understanding this difference is key when evaluating AI for regulated systems, where predictability and validation are paramount.
Machine learning (ML) works by identifying patterns in large volumes of historical data to make predictions or classifications. In regulated industries like healthcare, ML models are often trained using supervised learning, where labeled data, such as annotated radiology images, guides the algorithm to recognize specific features.
A neural network processes these inputs, adjusting internal parameters through a method called backpropagation until it produces reliable outputs. Once trained and validated with separate test data, the model can make consistent, repeatable predictions. These static models are ideal for applications requiring traceability and repeatability, like diagnostic tools or quality inspections.
Fortunately, FDA has already provided guidelines for AI and ML devices on predetermined change control plans.
AI is already making a measurable impact in quality management systems by streamlining time-consuming and repetitive tasks. One of the most common use cases of AI-driven productivity in quality teams is in documentation, where generative AI tools like ChatGPT can help draft and audit quality records with greater speed and consistency.
Quality teams can also enhance root cause analysis by using AI to evaluate fishbone diagrams and identify potential gaps or overlooked contributing factors. Predictive maintenance, another AI-driven function, is increasingly being used in manufacturing environments to detect equipment issues before they escalate into failures, improving overall reliability and reducing downtime.
Additionally, there is high scope for AI for CAPA management. AI can support faster and more accurate CAPA and non-conformance searches by analyzing large databases of historical records. These applications reduce human error, accelerate response times, and enable teams to focus on higher-value strategic tasks—ultimately improving compliance outcomes and operational efficiency.
The effectiveness of AI in knowledge work isn’t just anecdotal, it’s backed by credible research.
This productivity gain allowed legal professionals to redirect their time toward more complex legal challenges. Another comprehensive study by the Boston Consulting Group explored AI's impact in business consulting. Consultants were asked to conceptualize and develop new product ideas with and without AI. Those using AI delivered 40% higher-quality proposals, with less experienced consultants benefiting the most.
These findings suggest that AI doesn't just help seasoned professionals work more efficiently, it can also accelerate onboarding, upskill junior staff, and mitigate risks associated with inexperience, especially in quality-driven environments where adherence to processes is critical.
Justin walked through real AI demonstrations, from generating engineering designs for wind turbines to editing quality documentation using Canvas. These tools aren’t just proof of concept; they are already being used in regulated environments to improve first-pass yield, documentation clarity, and team collaboration.
So how can a quality-focused organization begin its AI journey?
For regulated industries, validation remains a top concern. While the FDA hasn't issued specific AI-QMS validation guidance (acknowledging the pace of change), their Computer Software Assurance (CSA) framework offers a risk-based blueprint. Key principles include:
Most importantly, AI tools should be used to augment—not automate—critical decisions, always maintaining a human-in-the-loop approach.
The second part of the blog is available here.
AI-driven productivity in quality teams has allowed streamlining documentation, root cause analysis, predictive maintenance, and CAPA management by automating repetitive tasks, improving accuracy, and accelerating response times.
Machine Learning produces static, repeatable outputs ideal for diagnostics, while Generative AI (like ChatGPT) creates new content, useful for drafting, summarizing, and brainstorming tasks. The former supports traceability; the latter, creativity.
Yes, with a risk-based validation approach. The FDA supports AI and ML in Software as Medical Device (SaMD) under frameworks like Computer Software Assurance (CSA) and predetermined change control plans.
Begin with low-risk, high-impact areas such as documentation review, training content generation, and search automation. Build confidence through pilot projects and scale gradually.
Quality Management with AI tools has shown productivity increases of 11–40% across industries, enabling professionals to focus on strategic tasks, accelerate onboarding, and reduce the impact of inexperience.
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