Clinerion Ltd Contact Details:
Main address: Margarethenstrasse 47 4053 Basel, Switzerland ,
Tel:+41 61 865 60 60 , E-mail: info(at) Website:

Clinerion Quality Risk Management System

Clinerion Quality Risk Management System

Cloud-based risk management system for controlling risks to clinical trial quality.

Clinerion Patient Recruitment System

Clinerion Patient Recruitment System

Optimized study design, precise site selection and faster patient recruitment for clinical research - in real time.

PRS Benefits

Accelerating Clinical Research for Pharmaceuticals.

Developing new medicines is risky: it takes a whole lot of time and money, with no guarantee of success.

Finding ways to improve efficiency, increase effectiveness and accelerate the process would generate huge savings in the cost of drug development and in the time needed to get medicines to the public.

Clinerion’s promise is to deliver radical efficiency savings to key clinical trials processes via high-technology, big data informatics solutions for health data. In the key areas of protocol feasibility testing, site strategy and site feasibility testing, and patient search, Clinerion’s solutions bring massive time and cost savings through access to 100%, real-time information on aggregated patient populations, across institutions and geographies. This leads to protocols being optimized using live data, finding 10-30 times more patients than through traditional methods, and getting site search results within minutes. Time-critical trials also become possible as the system runs in real-time, 24/7.

What Patient Recruitment System brings to Pharmaceutical Companies.

  • Clinerion saves the clinical research industry months in time and millions in costs during drug development in avoiding the need for study protocol amendments and in speeding up trial site selection and patient recruitment, i.e. finding enough patients within the target enrollment time.
  • Clinerion increases the efficiency of the clinical trial process by enabling patient search and selection of sites with real and complete information (no randomness, or guesswork).
Features Allows you to ... Benefits

Protocol design

Define your protocol using unlimited inclusion and exclusion criteria and using complex combinations of criteria based on demographics, diagnoses, medication, laboratory values and undertaken procedures.

Accelerate the protocol development process.

Protocol feasibility

Test and refine your protocol, live, against real hospital patient populations.

Make the protocol more relevant and realistic.

Finding potential trial sites Use your protocol to identify hospitals with patient populations which fit your criteria, live, and in a single query.

Make your trial more efficient: fewer sites with more patients.

Speed up site identification – results within minutes!

Patient search


When a hospital has become a trial site, research clinicians there can identify individual patients for recruitment.

Find typically 30 times more patients!

Patient enrolment 

Trial managers can keep track of patient eligibility and enrolment status. Real-time alerts on suitable patients, 24/7 – even up-to-the-minute walk-ins.

For benefits for hospitals and trial sites > 

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