This 4-session online course on Proactive Risk Management in Medtech covers ISO 14971 application throughout the medical device lifecycle. Learn to identify hazards, assess risks, and implement controls to meet MDR, IVDR, and FDA regulations. Ideal for Medtech R&D, Quality, and Regulatory professionals, with hands-on tool experience.

Subsidised rate: €1,285    Full cost: €1,975    Subsidised Rate for SMEs: €540 (contact us)

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.

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

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.

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

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

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

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

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

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

This course introduces the Minitab environment, teaching participants how to import, prepare, and visualize data using fundamental analytics tools like histograms and boxplots.

Subsidised rate: €186    Full cost: €295