Professional service
Clinical trialsSupport & Management
We are experts in the organisation of clinical trials. With our exceptional medical experience, we assure quality and reliability throughout the entire clinical trial process.
We care
We ensure that your clinical trial process flows efficiently
With a focus on project management in clinical trials for pharmaceutical and biotech companies, we ensure long-term and successful customer relationships.
1
Professional Teams
Our project leaders and coordinators support your team each step of the way during the drug development process – from start-up activities through to archiving.
2
Standard operating procedures
Rapid familiarisation with your Standard Operating Procedures and requirements ensures that we are ready to support your team from the get-go.
3
Extensive industry experience
Our comprehensive understanding of the regulatory environment, and our ability to “think outside of the box”, will drive your projects to the top.
Customer benefit
Comprehensive experience in clinical trial conduct
We have more than 10 years of experience supporting leading companies in the industry with their clinical trials in a variety of areas.
Our passion is the key to your success!
We offer you professional support with our expertise and hands-on approach.
News
Clinical Trials We Support Right Now
In our news section you can get an overview of the clinical trials we are managing and what the key outcomes are.
- general
ClinTriCare is delighted to welcome the addition of several new team members in the second quarter of 2025. These individuals contribute not only valuable professional expertise but also a distinctive spirit that enhances the collective strength and diversity of the organization. Their arrival represents another step toward cultivating a dynamic and forward-thinking work environment. Welcome to the team – we are excited for the journey ahead.
- general
ClinTriCare held its company meeting as a dedicated forum for knowledge sharing, strategic reflection, and organizational cohesion in Heidelberg. Key topics on the agenda included cybersecurity and the complex regulatory environment surrounding medical technologies. A keynote presentation entitled “Between Innovation and Regulation – The Authorization of Combination Products in Europe” offered deep insights into one of the most challenging and rapidly evolving areas of European Healthcare Regulation.