Find the Right AI Training Course for Life Science Professionals
Explore our portfolio of AI training courses designed specifically for professionals working in pharmaceuticals, biotechnology, cell and gene therapy, CMC, regulatory affairs, quality, manufacturing and medical devices. Learn how Artificial Intelligence and Generative AI are transforming life sciences whilst understanding practical applications, regulatory expectations and implementation strategies.
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Upcoming AI (Artificial Intelligence) Training Courses
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AI for Drug Development & Pharma Strategy
28 & 29 October 2026 | 2-Day Live Online Course
Original price was: £695.£556Current price is: £556.
Creating AI in Your Medical Devices: A Regulatory & Development Overview
2027 Dates TBC | 1-Day Live Online Training & On-Demand
Original price was: £350.£280Current price is: £280.
Tailored AI Training Programmes for Your Team
Whether your organisation is beginning its AI journey or looking to scale AI adoption, we design bespoke training programmes around your objectives. From AI awareness through to practical implementation, governance, validation and regulatory compliance, our experts help teams confidently adopt AI across research, development, manufacturing, quality, regulatory affairs and medical devices.
AI Training Across the Entire Product Lifecycle
Artificial Intelligence is transforming every stage of product development and commercialisation. Our courses cover AI applications across drug discovery, CMC development, manufacturing, quality assurance, regulatory affairs, pharmacovigilance and medical devices. We also explore AI governance, validation, data quality, risk management and evolving global regulatory expectations, enabling cross-functional teams to build a shared understanding of responsible AI adoption.
AI Training Designed Around Your Organisation
Every organisation is at a different stage of AI maturity. Whether you are exploring opportunities, developing an AI strategy, implementing AI tools or validating AI systems within regulated environments, we tailor programmes to your needs. Browse our AI course portfolio or contact us to discuss customised AI training for your organisation.
Why Choose Our AI Training
- Life Science AI Experts — Learn from industry professionals with practical experience applying AI across pharmaceuticals, biotechnology and medical devices.
- Practical AI Applications — Focus on real-world use cases, demonstrations and workshops rather than AI theory alone.
- Regulatory & Compliance Focus — Understand emerging expectations surrounding AI governance, validation, transparency, risk management and regulatory compliance.
- Implementation Support — Learn practical frameworks for introducing AI into regulated environments safely and effectively.
- Flexible Learning Formats — Choose from live online, classroom, hybrid, on-demand or bespoke in-house training.
Core AI Training Topics Covered
Our AI portfolio includes topics such as:
- Generative AI for life sciences
- AI in drug discovery and development
- AI for regulatory affairs
- AI in CMC development and manufacturing
- AI for analytical development and quality
- AI validation and trustworthy AI
- AI governance and compliance
- AI risk management
- Prompt engineering for life science professionals
- Large Language Models (LLMs)
- AI for scientific writing and knowledge management
- AI in medical devices and Software as a Medical Device (SaMD)
- AI strategy and organisational readiness
- AI implementation within regulated environments
Who Should Attend?
Our AI training is ideal for:
- Pharmaceutical professionals
- Biotechnology and cell & gene therapy professionals
- Medical device and IVD professionals
- Regulatory affairs teams
- CMC professionals
- Quality Assurance and Quality Control
- Manufacturing and operations teams
- Clinical development professionals
- Scientific and technical writers
- R&D scientists
- Project managers
- Digital transformation leaders
- Anyone looking to understand how AI is changing the life sciences industry
More Information About Our AI Training
AI Training Designed Specifically for Life Sciences
Artificial Intelligence is rapidly reshaping the pharmaceutical, biotechnology and medical device industries. From accelerating drug discovery and improving manufacturing efficiency to supporting regulatory submissions and scientific writing, AI is becoming an essential capability across modern life sciences organisations. Our courses focus on practical, responsible AI adoption within highly regulated environments.
Practical AI Applications
Rather than focusing purely on AI concepts, our courses demonstrate how AI can be applied to real industry challenges including document creation, literature reviews, regulatory intelligence, quality management, data analysis, knowledge management, process optimisation and decision support.
AI Governance, Validation and Compliance
Successful AI implementation requires more than technical capability. Our training explores AI governance, validation, risk management, human oversight, data quality and regulatory expectations to help organisations deploy AI responsibly within GxP and regulated environments.
Learning Outcomes
Participants will learn how to:
- Identify valuable AI opportunities within life science organisations
- Apply Generative AI effectively in day-to-day work
- Understand AI risks and governance principles
- Improve productivity through AI-assisted workflows
- Build AI implementation roadmaps
- Understand current and emerging regulatory expectations
- Evaluate AI tools for regulated environments
- Increase confidence using AI responsibly
See What Past Attendees Think
Free Pharmaceutical Resources
We provide a wealth of free resources designed to elevate your pharmaceutical career, whether you work in regulatory affairs or CMC. Delve into our exclusive free trainer interviews, thought-provoking articles, guides, top tips, career advice and much more below.
Pharmaceutical Regulatory Affairs Free Module 1 Training Sessions
Free Module 1 Training for Regulatory Affairs Professionals
Many of our regulatory affairs training courses offer a free-to-attend Module 1, giving you valuable insights and a preview of the full course experience. Browse the available courses below and register using the form provided. Once registered, you'll receive joining instructions for the live session...
Pharmaceutical Free Module 1 Training Sessions
Free Module 1 Training for Pharmaceutical Professionals
Many of our pharmaceutical training courses offer a free-to-attend Module 1, giving you valuable insights and a preview of the full course experience. Browse the available courses below and register using the form provided. Once registered, you'll receive joining instructions for the live session –...
Pharmaceutical Regulatory Affairs: A Complete Guide to Roles, Submissions and Global Agencies
Understand pharmaceutical regulatory affairs from development to approval—covering FDA, EMA, submissions, and career pathways.
A practical introduction to pharmaceutical regulatory affairs, covering what the function does, how medicines move through regulatory systems, the agencies involved, and how professionals build careers in the field. Learn more about our full regulatory affairs training courses - here What Is Pharmaceutical Regulatory...
Navigating EU Marketing Authorisation: Key Routes and Procedures Explained
Centralised vs Decentralised vs Mutual Recognition Procedures
Marketing authorisation is a critical step for any medicinal product entering the European market. Unlike the US, where the Food and Drug Administration (FDA) handles approvals, Europe offers several complex regulatory pathways. This article explores the various marketing authorisation routes available in the European Economic…
What Is IDMP and Why Is It Transforming Pharmaceutical Regulatory Affairs?
From Regulatory Documents to Structured Data: Understanding the Future of Medicinal Product Information Management
The pharmaceutical industry is undergoing a fundamental shift in how medicinal product information is managed, exchanged and used. For decades, regulatory processes have been largely document-driven. Product information has been captured within regulatory dossiers, application forms, PDFs and spreadsheets. While initiatives such as the Electronic Common...
What Is Pharmaceutical Quality Assurance? A Complete Overview
Understanding QA in Pharma: Roles, GMP Compliance, Risk Management and Why Quality Assurance Is Critical to Patient Safety
In the pharmaceutical industry, quality is not just about meeting specifications or passing inspections. It is about ensuring that every medicine reaching a patient is safe, effective, consistent, and fit for purpose. That responsibility sits at the heart of pharmaceutical quality assurance (QA). Whether manufacturing...