Pharmaceutical Training Courses

Find and Register for a Pharmaceutical Training Course to Develop Your Skills

Explore our pharmaceutical training course portfolio covering topics such as regulatory affairs, CMC, manufacutring, development, and operations. Whether you work in R&D, formulation, quality, regulatory affairs, or operations, we offer training courses that bridge theory and real-world application across global markets.

Why Choose Educo Life Sciences?

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People Choose Educo Every Year

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From 180 Different Companies

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We Deliver Over 100 Courses Every Year

97%

We Achieve 97% Positive Feedback

Upcoming Pharmaceutical Training Courses

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Original price was: £595.Current price is: £476.
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Original price was: £1,395.Current price is: £995.
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Team Training Solutions

We support manufacturing, quality, process and analytical leaders to improve the technical skills and knowledge of their employees, so they are equipped to overcome challenges and meet business objectives. Working together, we design and deliver technical training courses that align with your learning requirements and business goals. For more information about how we can support your team please get in touch.

 

Could your manufacturing team benefit from any of the courses listed above? Or maybe a topic which is not highlighted? We would be happy to discuss your objectives and see how we might be able to help.

 

Learn more about our team training solutions. 

Why Choose Our Pharmaceutical Training

  • Trainer Expertise — Our instructors bring hands-on experience from large pharma, small biotechs, CROs, and regulatory agencies, having led development, analytical, GMP, and regulatory projects.
  • Practical Focus — With case studies, interactive workshops, and real project scenarios, you’ll learn to connect scientific theory to daily challenges in pharmaceutical development and operations.
  • Global Regulatory & Market Perspective — Our content reflects regulatory expectations in EMA, FDA, ICH, and global harmonisation trends to help your team operate across jurisdictions.
  • Post-Learning Support — You’ll have access to reinforcement materials, detailed reference guides, regulatory updates, and ongoing support to ensure long-term retention and practical application.
  • Flexible Delivery Formats — Choose from live online, classroom, hybrid, or on-demand formats so the training aligns with your schedule or your team’s needs.

Core Pharmaceutical Training Topics Covered

In our regulatory portfolio topics include:

  • Drug product development & formulation strategies
  • Pharmaceutical analytical methods, validation & stability
  • Dissolution, impurities, and degradation pathways
  • GMP operations, quality systems & data integrity
  • Technology transfer, scale-up, and process optimisation
  • Regulatory & lifecycle topics: CTD/Module 3, variation, post-approval changes
  • Risk management (ICH Q9), quality by design (QbD)
  • Manufacturing controls, process validation, qualification
  • Labelling, packaging, serialization & regulatory compliance
  • Technology trends: continuous manufacturing, process analytics

Who Should Attend?

Our training courses are ideal for:

  • Regulatory affairs professionals at all levels (beginners to advanced)
  • Project leaders or cross-functional professionals bridging science and regulation
  • CMC, QA and development staff needing regulatory awareness
  • Project managers and cross-functional teams supporting submissions
  • Biotech and pharma companies preparing for global market entry
  • Newcomers to pharmaceutical development or professionals seeking to refresh knowledge

More Information About Our Training

Comprehensive Pharmaceutical Training Across Disciplines

The pharmaceutical industry is scientifically and regulatory complex. Our training programmes span core domains such as formulation, analytics, process development, technology transfer, GMP operations, and regulatory science. Whether you’re working on small molecules, biologics, or advanced therapies, we ensure your technical foundation is strong.

Analytical & Stability Expertise

Analytical techniques, method validation, stability protocols, dissolution, and impurity profiling are often critical bottlenecks in development. Our courses equip you with best practices, industry standards, and regulatory expectations to ensure your methods are robust and compliant.

Regulatory Integration & Lifecycle Management

Linking development with regulatory strategy is essential. Our modules cover CTD/Module 3 (CMC) dossier contributions, variation management, post-approval changes, labelling, serialization, and maintaining compliance through the product lifecycle. We also address how regulatory expectations evolve globally.

Outcomes & Benefits for Your Team

Participants gain capabilities to:

  • Design and execute robust development and manufacturing strategies
  • Develop and validate analytical methods in compliance with regulatory standards
  • Prepare strong regulatory submissions and manage post-approval obligations
  • Harmonise development, quality, and regulatory teams around common frameworks
  • Reduce development risk, regulatory delays, and audit non-conformities

See What Past Attendees Think

Understanding EU Regulatory Affairs
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“The course was well structured, the trainer was extremely professional, friendly and presented well the material. Educo support team and host were very responsive and easily approachable! Overall add-value course to follow.
AIM 
Completing the Quality/CMC Module of the CTD
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“Great course in particular for the registration of a new product. The trainer is full of knowledge and we can be fully confident with him. The portal access is easy to use and helpful. I would suggest to have already some technical background to attend this course”
Ethypharm
Validation, Verification and Transfer of Analytical Methods
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“Mark Powell is a truly talented person that can pass through complicated information to anyone. His presentation, training and advice were valuable that I can look back into when in need. Very satisfied to follow his training and glad I joined the live session and not the online course”
Patheon (Thermo Fisher)
Regulatory Lifecycle Management in The EU (Filing Variations)
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“I just recently enrolled in a Regulatory Affairs role and my RA is not very solid; nevertheless, I was able to follow easily the lecture provided by the trainer, who was very clear and competent; the material shared during the lesson was very well prepared and detailed and it is a very helpful resource also to look at for future reference. Great course and absolutely great trainer”

Norgine 
Understanding US FDA Regulatory Affairs
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“Great course to understand US FDA specific interactions with the Applicant/MAH from development to life cycle management.”
Blue Pharma
CMC Essentials: An Overview of CMC Development
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“The Educo trainers are not only very knowledgeable in their fields, but have a talent for teaching. They know how to present the topics in a way that is immediately useful for the projects that we are working on. Thank you Educo!”
Batavia Biosciences

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) | Free Module 1 Training Sessions

Find a Free-to-Attend Training Session

Many of our 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 – or,...

Breaking into Biotech R&D: Insights on Drug Development, AI & ATMPs

Expert Advice from Educo Trainer Gareth Willis

What does it take to thrive in the ever-evolving world of pharmaceutical R&D? Gareth — a biotech leader, educator, and former translational researcher — has built a unique career across academia, big pharma, and early-stage biotech. In this exclusive interview, he shares how he made...

From Compliance to Confidence: Building Analytical Methods That Perform in the Real World

A lifecycle approach to method validation that ensures reliability, robustness, and real-world performance.

In regulated pharmaceutical environments, method validation is a cornerstone of quality assurance. Yet many validated methods still fail to perform reliably in routine use. This disconnection between regulatory compliance and real-world functionality is all too common. The good news? With a more pragmatic and risk-based...

How to Complete CTD Module 3: CMC Regulatory Q&A for Pharma & Biotech

Q&A’s from the Free Module 1 Training Sessions

The Chemistry, Manufacturing, and Controls (CMC) section of a regulatory dossier is critical in ensuring product quality and regulatory compliance. Educo delivers the course “Completing the Quality/CMC Module of the CTD” which includes a free-to-attend module 1 training session. Over the years, attendees of the...

Regulatory Affairs for Combination Products: Comprehensive Q&A

Q&A’s from the Free Module 1 Training Sessions

Combination products pose regulatory difficulties as the requirements of medical devices must merge with pharmaceuticals and biotech. As biotech and advanced therapeutics grows, so too does the need for specialised device delivery systems resulting in an increase in combination products. Similarly, device companies are increasingly...

Challenges and Strategies in Regulatory Lifecycle Management

Focus on CMC Changes and A Global Perspective

Regulatory lifecycle management is an essential aspect of maintaining product compliance, particularly when dealing with Chemistry, Manufacturing, and Controls (CMC) changes. However, managing these changes on a global scale introduces unique challenges due to differing regulations across countries. In this article, we explore the key…

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