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Seeking investment? – The relevance of the 4Cs from an investor’s perspective

Seeking investment? – The relevance of the 4Cs from an investor’s perspective

by Lea Rebholz | Sep 26, 2023 | Blogbeitrag (EN)

Questions about the 4Cs and their interrelations play a central role in the development of a plausible business model in the healthcare sector. Obviously, networked 4C knowledge is also a key advantage in fundraising. We spoke to Christian Kraft, Director M&A and...
Selective contracts as an opportunity for startups to enter the market? – Insights by Experts of BKK Linde

Selective contracts as an opportunity for startups to enter the market? – Insights by Experts of BKK Linde

by Lea Rebholz | Aug 10, 2023 | Blogbeitrag (EN), C1

74 million people in Germany, and thus almost 90 % of the population, have statutory health insurance. So when it comes to the question of how to bring a new, innovative product to market, medtech start-ups often find a quick answer in the statutory health insurers...
From an auditor’s perspective: pros & cons of eQMS

From an auditor’s perspective: pros & cons of eQMS

by Dietmar Schaffarczyk | Jul 17, 2023 | Blogbeitrag (EN), C2

As the healthcare industry continues to grow, it is essential to ensure quality and compliance with regulatory standards. Electronic Quality Management Systems (eQMS) are increasingly being used to manage and maintain quality processes in organizations. This article...
Medical device on the rocks – The importance of design freeze for a medical device

Medical device on the rocks – The importance of design freeze for a medical device

by Henrike Stutzki | Nov 18, 2022 | Blogbeitrag (EN), C3

As an early-stage startup, you are usually in the middle of your development process in order to implement your innovative idea  as a first prototype and later as the final product ready for series production. At the end of a development phase, there is a design...
Clinical data for the clinical evaluation of a medical device – How to proceed?

Clinical data for the clinical evaluation of a medical device – How to proceed?

by Henrike Stutzki | Jul 12, 2022 | Blogbeitrag (EN), C3

The requirements for clinical evaluation and the significance of clinical data for medical devices have become greater as a result of the MDR – everyone knows that by now. But what does this mean for startups in the medtech sector? And what do you have to...
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