About us

At Clinipower I focus on constantly scanning customer needs and finding new experts to join our team. When I founded Clinipower, my idea was to offer various customers the kind of best industry expertise for which only large companies usually have resources. A topic close to my heart is spreading the culture of patient safety within the high tech industry.

My biggest dream is to go global on a larger scale: the Finnish know-how in health care digitalization is very strong, and taking it to international markets is something we are eager to facilitate.

I specialize in managing medical software development projects. I often describe a product development project like this: first, you need to find the forest to get lost in, and then find the path to get out. Product development is pruning and trimming until you get to the finished product – and it may often be different from the developers initial idea. From the first steps on, it’s important to remember that top-notch software can only be created in tight co-operation with the end users.

I’ve been a startup entrepreneur three times. I’m also contributing to the development of industry standards in the HL7 Finland Association and representing Finland in a work group of the HL7 International Association.

I specialize in health tech quality and risk management, regulatory compliance and life cycle management of software products. I want to do my part to support Finnish companies in the jungle of regulation, so that new healthcare products can be launched successfully.

For me, building a quality system together with a customer is always an interesting process. Patient safety is the cornerstone of health tech, and it should be kept in mind through every phase of product development. Although there are plenty of regulative requirements, they can be integrated as a seamless part of a customer’s practice by setting up clear operational models and procedures.

My experience and know-how relate diversely to quality management and regulation, innovation, technical writing, information security, and sales in the health technology field. Working in this field motivates me as it aims at helping people.

I am interested in working with quality management systems. As the role of regulation strengthens and becomes more and more precise, the workload of regulatory specialists and quality managers increases. I want to support industry newcomers with services that help them get to development work with a low threshold.

My specialty is clinical evaluation, user experience and usability of medical devices. I get to use my experience as an intensive care nurse by understanding the end use of medical equipment and the environment in which it is used. A safe and useful medical device requires a good knowledge of the users and the operating environment.

In my work, I strive to promote a safety culture and solid usability. Manufacturers, health care organizations and professional users play a key role in ensuring these.

I specialize in product and service design, conceptualization and evaluation. When the goal is to develop a successful product, user experience and safety are the key areas to consider.

Health tech is basically about improving people’s life and their life management, and that’s what I like to be involved in. What also fascinates me in this industry is that it brings together two worlds: how to promote innovation and agile product development and embed the strict regulatory requirements into it.

I specialize in product management and business development. Digital innovations can help people very much, if they are done the right way, and that takes a dedicated team.

I’ve worked all over the globe facilitating and building product development teams. I am from Salzburg, Austria, but I think of myself as a citizen of the world. I like being able to spark an idea, get people committed to think together – even challenge them a little if need be. I create trust by being totally committed myself: I only take on projects I believe in, so I am always all in.