Rolling up our sleeves to work with our clients to make healthcare better: below we’ve picked a handful of success stories out of the more than 2,500 projects we’ve delivered for clients so far.
Sharing insights on making healthcare better: Sometimes, we also share our knowledge or perspective on a salient topic with the world, in the form of insights or whitepapers.
MDR for Supply Chain 2021
The new European Regulations on Medical Devices (EU 2017/745) increasingly impact healthcare and contribute to an industry-wide uncertainty on compliance. Due to Switzerland’s bilateral agreements with the EU and the de-facto adoption of the EU regulations, there is a need for the Swiss healthcare industry to identify the best way to ensure compliance rapidly and efficiently with these regulations.
We prepared an overview of our Organisational Change Management Services from Arcondis. Here we cover the challenges and opportunities that come with OCM
Embracing change has never been more relevant: each industry segment within Healthcare and Life Science is currently experiencing a seismic shift in their traditional ways of working, tools, and procedures. The digital transformation continues and incites change within every department.
Health Campus 2030
With our unique focus on the Life Sciences and Healthcare sectors, we’ve stayed at the forefront of current trends and developments in these industries. Growing alongside our clients over the last two decades has given us a unique inside view and understanding of the specific challenges, needs and successful transformation approaches of key players
Computer Software Assurance (CSA)
This paper is about the new FDA guideline on Computer Software Assurance (CSA), the differences to Computer System Validation, the benefits of CSA, and how Arcondis can support you with introducing CSA in your company.
We interviewed our OCM experts to find out how change has to be managed, what pitfalls can be avoided, and why change management improves long-term success.
Software as Medical Device
Nowadays, there is almost no active medical device without some interaction with software. Since the introduction of the European Medical Device Regulation 2017/745 (MDR) and In-Vitro Diagnostic Medical Devices Regulation 2017/746 (IVDR), the industry talks about the impact and classification of Medical Device Software
We improved tissue sample analysis with an AI solution
We implemented an AI solution that pre-scans tissue samples, reducing the workload for scientists in research, improving analysis and reducing errors, and ultimately ensuring drug safety and efficacy for patients.
We protected our client’s proprietary information while ensuring transparency in food safety
We developed a machine learning algorithm to create an automated redaction process which secures proprietary information while being compliant with new EU regulations.
We helped our client personalize engagement with physicians
We ensured that physicians have a much improved user experience with the manufacturers of the drugs they prescribe to the patient.
We accompanied our client on the road to smart commercial production.
Through strong cooperation, we defined and improved low-maturity processes and workflows, making the manufacturing process faster and safer for patients.
Rethinking Swiss Health Insurance
Swiss healthcare business sustainability is at risk: by 2030, c.a. 30% of the Swiss population might struggle to pay their mandatory insurance premium.