Tuleva koulutus 13.4. "Tuotteen rekisteröinti, ylläpito ja seuranta julkaisun jälkeen"

Ilmoittaudu mukaan

For health technology innovations, the road to global success may be long.

We’ve walked the walk. We know how to help you at every turn.


Product development and usability engineering of medical devices, risk management and patient safety, regulatory requirements and quality management systems are Clinipower’s core competences.

  • Are you thinking of developing a product or software?
  • Is your organization planning to take a leap into health technology?
  • Do you recognize the need to change your organization’s operational culture?
  • Do you need more information about the impact of regulatory changes on your business?

We have the answers. We are offering our experience, knowledge and skills for your benefit – plus the spirit of making things happen that is our hallmark.

Contact us, and let’s figure out together where to start!


Responsibility expert Jaana Pirhonen complements Clinipower’s expertise
Posted on 22.12.2023

Considering environmental and responsibility issues in the medical device market is worthwhile. It is an investment in the future in a world where more and more consumers...

International master’s program provides capabilities for the digital transformation of healthcare
Posted on 22.12.2023

We are pleased to announce that we are participating in a significant education project, “Master of Managing Digital Transformation in the Health Sector” (ManagiDiTH)....

IVD Regulation is coming – are you ready?
Posted on 20.05.2022

Thursday 26th of May 2022 is a significant day for those operating with in vitro diagnostic (IVD) medical devices in the European Union (EU). This is the date of application...


Quality and regulation

We help you build an ISO 13485 quality management system. We offer you an outsourced quality manager and assist with CE-certification and audits.

Usability and service design

We support you in concept development and evaluation. We do usability testing and design sprints.

Product development and processes

We guide organizing product development in practice and according to requirements. We support you throughout the journey to market.

Management support and business

We assist you in organizational development. We help you anticipate critical points of regulation. We offer professional resources for your service.

Tilaa uutiskirje

Pidämme sinut ajan tasalla olennaisista aiheista terveysteknologian alalla. Saat tietoa palvelutarjonnastamme ja koulutuksista, joilla tuemme menestystäsi.

About us

Maija Laukkanen
CEO, Sales
Pekka Kola
Senior Advisor, Technology and Architecture
Kimmo Vauhkonen
Senior Advisor, Quality and Regulation
Raimo Asikainen
Senior Advisor, Quality
Kalle Schnitzer
Senior Advisor, Clinical Evaluation and Usability
Jaana Pirhonen
Senior Advisor, Responsibility
Juha Kaasinen
Senior Advisor, Usability and User Experience
Christian Wagner
Senior Advisor, Product Portfolio Management
Aki Tirkkonen
Senior Advisor, Project Management and Solution Architecture
Sylvia Syvänen
Research Trainee