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Clinius offers internationally accredited training 24/7 for healthcare technology

Together with its partner Comply Guru, Clinius offers a new, internationally accredited training service in Finland. Available anytime and anywhere (24/7) eLearning will cover the key legislative requirements related to healthcare technology (MDR, IVDR, FDA QSR and MDSAP) as well as standards ISO 13485 and ISO 14971. The training ranges from the foundation level up to practitioner and lead auditor level. eLearning offers a learning environment with interactive and engaging content, continuous learning monitoring and a final exam to obtain certification.

In more demanding trainings, eLearning is combined with instructor-led workshops. In this kind of hybrid (Blended Learning) format, the trainees are first assured of the underlying theory and knowledge, so that the workshop phase can more effectively focus on practical application and acquisition of skills. In this way, a deeper assimilation of the content is promoted.

"Our partnership offers flexible and effective, internationally accredited training for companies operating in Finland and their personnel," say CEOs Kelly and Maijala together. With Online Learning, you can improve your knowledge and skills regardless of time or place. "Clinius can supplement this knowledge gained from the trainings by consulting on company-specific challenges," continues Maijala.

Comply Guru Ltd

Multi-Accredited Innovation Leader in eLearning for the Medical Device Industry

Our mission is to transform training & simplify the complex landscape of international standards and everevolving regulations. Comply Guru is first in the world to focus on Internationally Accredited eLearning (24/7) on Standards & Regulations and Blended Learning for Auditor Training for the Medical Device Industry.

For information: CEO Eoin Kelly, +353 61 529100, ekelly@complyguru.com, www.complyguru.com/en-fi/

Clinius Oy

Clinical device trial and Quality Management specialist

Clinius is a Finnish pioneer in clinical device trials, a device CRO with focus on clinical device studies, product documentation and quality systems according to ISO 13485. We help companies in the health and well-being sector in understanding customer needs and in meeting the official requirements for products (MDR and IVDR).

For information: CEO Miikka Maijala, +358 40 509 6160, miikka.maijala@clinius.fi, www.clinius.fi/en