Discover some of our success stories and insights.

Arcondis’ Operational Excellence solution is specifically designed for life sciences companies that want to improve operational performance, productivity and cost efficiency. With over 30 years of unrivalled experience in pharma operational excellence, we are uniquely placed to transform operations and instill a culture of continuous improvement that consistently exceeds our clients’ expectations. With our client-centric approach and experienced team, we identify areas for improvement and deliver exceptional results that go beyond what our competitors can offer. 

At Arcondis, we have developed a deep understanding of the unique challenges faced by the Life Science industry, particularly in pharmaceuticals and MedTech. This understanding has led us to specialise in the field of qualification and validation, as we recognise its pivotal role in guaranteeing the safety and effectiveness of end-to-end processes throughout the entire product life cycle

To support your success with AI projects, we have established a maturity scale on which you can grade your organisation according to five operational Work areas and three support Drivers. Once you know where you stand, you can follow our recommendations and assessment to achieve results more rapidly, efficiently, and safely.

In this viewpoint, we outline a dynamic patient engagement by using various communication channels and the potential use of omnichannel engagement to integrate these channels. We conceptualize a novel patient care journey where multiple web-based and offline communication channels are integrated through a “digital twin.”

©Agata Blasiak, Yoann Sapanel, Dana Leitman, Wei Ying Ng, Raffaele De Nicola, V Vien Lee, Atanas Todorov, Dean Ho. Originally published in the Journal of Medical Internet Research (https://jmir.org), 16.11.2022.

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

Read our pocket guide to find out more about R&D in the 21st century with Future Labs; Effective automation with Industry 4.0; Correctly handling risks with Quality Management; and Qualifying/validating design, processes & systems with CQV/CSV.

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.

Our experts give their views and insights on relevant topics, including: Industry 4.0; Annex 1; My Green Lab initiative; Computer System Validation (CSV); Quality Management and Future Lab.

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 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.

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.

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

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