Training

🡨 Coaching PRRC 🡪

Expert Training for Medical Device & IVD Regulations

Understanding the complex regulatory frameworks for medical devices and IVDs requires more than just theory — it demands practical, applied knowledge across the entire product lifecycle.

At JREG, we specialise in training programmes that help manufacturing companies and their teams navigate requirements from early feasibility through to post-market surveillance.

Our courses are delivered by experienced regulatory professionals with backgrounds in quality assurance, design & development, and risk management.

Tailored Learning That Fits Your Business

We design bespoke training that is customised to your products, markets, and team experience levels. Whether you need a comprehensive introduction to ISO 13485 and QMS requirements, focused sessions on risk management (ISO 14971), or guidance on technical documentation for MDR and IVDR, our programmes are relevant, practical, and directly applicable.

Training can be delivered virtually or onsite, as short modules, half-day workshops, or full programmes, depending on your needs.

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Frequently Asked Questions

We offer flexible training on regulatory affairs, quality management systems, clinical evaluations, EU MDR, UK regulations, ISO 13485, and global compliance frameworks. Whether you’re new to regulatory or need to stay current, we’ve got you covered.

Our training is designed for teams at all levels — from new starters needing foundational knowledge to experienced professionals requiring updates on recent regulatory changes.

Yes. We customise our sessions to match your specific device types, markets, regulatory status, and team needs.

Training can be delivered in-person or virtually, as one-off sessions, short modules, or full programmes.

Yes. We understand that training budgets can be limited, especially for smaller businesses. We’ll work with you to find a solution that balances quality with affordability.

Popular training topics include:

  • EU MDR and UKCA regulatory requirements
  • ISO 13485 and QMS essentials
  • Technical documentation
  • Clinical evaluation basics
  • Post-market surveillance and vigilance
  • Audit readiness

Sessions can range from short 1–2 hour modules to full-day workshops, depending on the topic and your team’s availability.

Yes. We can offer coaching or consulting support to help your team apply what they’ve learned and embed knowledge into daily processes.

Absolutely. Our training is developed and delivered by experienced regulatory professionals who stay up to date with the latest changes and interpretations.

Simply get in touch. We’ll schedule a short discovery call to understand your needs and put together a tailored training plan that suits your timeline and budget.

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