Our industries
Pharma / Biotech
Regardless of your location or needs, we will provide a high-quality flexible solution with anything from full service to individually tailored packages. We have clients throughout the world and are used to working across time zones.
We can support your entire product development journey from early development through pre-clinical and clinical phases to post-marketing and continued clinical studies or RWE for example.
Product development requires extensive documentation to ensure reliable results and compliance with local and international regulations. Our team of experts has a wealth of experience covering all GxPs and ISO standards across the life science and health technology sectors from non-clinical and clinical trials, manufacturing, distribution and safety to support you with any challenge.
MedTech / IVD
Our experienced team of Medical Device Managers support you from concept to commercialization with hands-on product development
experience in all phases of development and in compliance with MDR and IVDR.
We provide you with tailored advice and support in anything from, for example, developing your strategy to clinical/performance evaluation, through CE mark, Notified Body audits and commercialization with post-marketing regulatory expertise.
590 +
clinical trials
150 +
employees
20 +
therapeutic areas
6
countries