Innokas Medical Business Blog

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How effective tools, competences and ways of working can have an impact on achieving more agile development cycles for medical devices?

MedTech as business is changing and getting more complex. For example, the technical complexity and regulatory requirements are something that are increasing as we speak. In addition, the user...

Developing software for regulated medical devices requires considerable expertise and fine-tuned testing procedures

We’re living in an amazing world where the new technologies and the science itself enable new kinds of miracles happen in saving peoples’ lives and in improving their well-being. In recent years,...

Choose a partner with substantial added value and concrete benefits

MedTech as a business is changing and getting more diverse. For example, the technical complexity, forms of digitization and regulatory requirements are something that are increasing as we speak....

Co-creation and standardized working methods bring agility to the regulated MedTech world

MedTech as business is changing and getting more complex. For example, the technical complexity and regulatory requirements are something that are increasing as we speak. At the same time there is...

How to choose the right co-creation partner to save both time and money when designing and developing medical devices?

MedTech business is changing and getting more diverse. The technical complexity, caused mainly by digitization, is increasing. New technologies are being introduced at faster pace, the impact of...

Sales has started for Otivio’s FlowOx 2.0 device

FlowOx 2.0, developed in co-creation between Norwegian company Otivio AS and Innokas Medical, has now reached a significant milestone as the device has received CE mark and the sales has started....

Innokas Medical strengthens its expertise in project management and software development and testing

Innokas Medical has further reinforced its know-how in medical device design and development. Two new resources have joined Innokas’ SW development team, while the teams of project managers,...

Top 10 benefits of applying appropriate Design Controls to your medical device development process

In short, Design Controls (or the practices of design and development, as in ISO 13485) refers to the application of a set of formal quality practices and procedures to the conduct of product...

How to shorten the medical device development cycle in practice?

MedTech business is changing and getting more diverse. The technical complexity, different forms of digitalization and related regulatory requirements are increasing as we speak. And there is the...

Save your time and money when designing and developing medical devices: choose a partner with substantial added value and more concrete benefits

MedTech as a business is changing and getting more diverse. For example, the technical complexity, forms of digitalization and regulatory requirements are something that are increasing as we...

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how to ensure the quality compliance of your medical product

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