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This 4 half-day online program covers biological evaluation and chemical characterisation of medical devices, focusing on EU/US biocompatibility. Learn to create Biological Evaluation Plans, close gaps, interpret test results, and understand the link to risk management, toxicology, and material characterisation.

Subsidised rate: €566    Full cost: €755

Quality Training

Biological Evaluation of Medical Devices, including Chemical Characterisation

Biological Evaluation of Medical Devices, including Chemical Characterisation

This one-day virtual course, CQI & IRCA Certified Internal Auditor Training (ISO 13485:2016), equips quality professionals with skills to plan, conduct, report, and follow up internal audits per ISO 19011. Prior QMS/ISO 13485 knowledge is required; an optional foundation course is available. A recognised certificate is awarded upon completion.

Subsidised rate: €387    Full cost: €595

Quality Training

Internal Auditor Training ISO 13485:2016

Internal Auditor Training ISO 13485:2016

CQI & IRCA Certified Lead Auditor Training (ISO 13485:2016). Blended learning for quality professionals to audit QMS against ISO 13485. Gain an internationally recognized Lead Auditor certificate

Subsidised rate: €813    Full cost: €1,250

Quality Training

Lead Auditor Training ISO 13485:2016

Lead Auditor Training ISO 13485:2016

The MSc in Medical Technology Regulatory Affairs is a two-year, part-time Level 9 programme designed for professionals working in the Medtech sector. Developed in collaboration with industry experts, it equips regulatory affairs personnel with the knowledge and skills to navigate complex global regulations, while also building key competencies in areas like clinical evaluation, technical writing, and quality systems. Delivered primarily online, the course includes modules on EU and US regulatory affairs, risk management, post-market surveillance, and more. A dissertation is completed in the second year, with a strong emphasis on real-world application in a highly regulated industry.

Subsidised rate: €8,914   Full cost: €12,555

Quality Training

Masters in Medical Technology Regulatory Affairs

Masters in Medical Technology Regulatory Affairs

Irish Medtech Skillnet, with ATU Galway, offers a Postgraduate Certificate in End-to-End Sterility Assurance. Designed for sterility assurance scientists and quality professionals, this program covers sterilisation methodologies for medical technologies, including industrial microbiology, biocompatibility, and cleanroom operations, via blended learning.

Programme commences 26th of January.

Cost: Full price: €4,500 Subsidised price: €3,195

Quality Training

Postgraduate Certificate in End-to-End Sterility Assurance (L9)

Postgraduate Certificate in End-to-End Sterility Assurance (L9)

Quality Training

Effective Report Writing

This live online course (two half-days) helps technical professionals create clear, concise, and impactful documentation. Learn to plan, structure, and refine documents, plus explore storytelling, AI prompts, and best practices for editing. Ideal for quality managers, engineers, and scientists, it shows how effective writing boosts efficiency and reputation.

Subsidised rate: €295      Full cost: €370

Quality Training

Effective Report Writing

Effective Report Writing

 Developed with the Irish Medtech Association's Sterility Forum and ATU Galway, this blended learning program provides advanced expertise in medical technology sterility assurance. Participants gain in-depth knowledge of microbiology, biocompatibility, sterility innovation, regulatory compliance, and leadership. Ideal for graduates of the PGCert in End-to-End Sterility Assurance seeking senior roles.

Programme commences January 27th 2026

Subsidised rate: €3,900    Full cost: €5,500

Quality Training

Master of Science in End-to-End Sterility Assurance

Master of Science in End-to-End Sterility Assurance

Comply Guru offers this self-paced online course on Medical Device Risk Management based on ISO 14971:2019, providing a comprehensive overview of risk management processes and techniques for medical devices. This eight-hour program is designed to give learners a thorough understanding of the standard's history, purpose, and key terminology.

Subsidised rate: €312    Full cost: €495

Quality Training

Medical Device Risk Management based on ISO 14971:2019 Foundation

Medical Device Risk Management based on ISO 14971:2019 Foundation

This blended learning program trains and certifies Life Sciences employees in Continuous Improvement methodologies like Lean and Six Sigma. Participants gain a thorough understanding of Lean principles, covering topics such as Value Stream Mapping, 5S, and problem-solving to implement improvements in their work areas.

 

Quality Training

Continuous Improvement in Manufacturing

Continuous Improvement in Manufacturing