Discover some of our success stories and insights.

This white paper focuses on how to drive digital engagement with a fine-tuned CIAM strategy that balance between customer experience and the security/compliance aspects, keeping in mind the special needs of the Pharma and MedTech industries.

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.

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

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.

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 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 developed a machine learning algorithm to create an automated redaction process which secures proprietary information while being compliant with new EU regulations.

We ensured that physicians have a much improved user experience with the manufacturers of the drugs they prescribe to the patient.

Through strong cooperation, we defined and improved low-maturity processes and workflows, making the manufacturing process faster and safer for patients.

Swiss healthcare business sustainability is at risk: by 2030, c.a. 30% of the Swiss population might struggle to pay their mandatory insurance premium.

Our dashboard solution enables physicians in hospitals to spend more time with patients instead of sifting through data.