At the Clinical Competence Centre (3C), we provide resources and expertise to elevate and streamline research projects of medical professionals, so they can keep their focus on patient care while doing high-quality research. We ensure rigorous standards, participant safety, and data integrity.

Our Mission

With the focus on patient care, medical professionals develop a unique perspective. Their day-to-day interactions with patients reveal subtle connections between illnesses and other aspects of a patient’s life – insights often missed by others. These observations stimulate research questions, prompting further exploration of these relationships. We’re here to empower both medical professionals and researchers to turn those questions into reality, Knowledge about the resources and guidance they need. We help to:

  • Improve the quality and efficiency of clinical research and trial management,
  • Inform about obligatory national/ international registration and regulations,
  • Increase the chances of securing research funding,
  • Streamline research projects through efficient project management and resource allocation,
  • Communicate research findings more effectively.

Our tailored support allows medical professionals to maximize patient care time while publishing in top-tier journals and ultimately maximise positive health care impact.

Our Vision

Our core beliefs are based on a democratic access to research resources and knowledge, ensuring that all researchers, regardless of background or experience, have access to the tools they need to create impactful research. We support collaboration, best scientific practices and knowledge sharing to advance clinical research. To be a trusted advisor you can rely on, we provide research expertise and build long-term partnerships that drive your success to enhance the quality and impact of clinical research.

Our Objective

Our objective is to facilitate high-quality research that aligns with Austrian (BASG – Austria; AGES) and European (EMA) regulatory and ethical standards. We aim to enhance the likelihood of positive study outcomes and mitigate risks for participants and researchers involved in controlled clinical trials.