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Patients comes first

We believe that patients’ needs are not sufficiently taken into account by healthcare stakeholders. The interest of patients and their families and friends is our first priority in all our partnerships with companies and academia.

We wish to provide patients with better solutions, while encouraging the co-creation of efficient services and helping the healthcare industry meet the needs of patients and their families more effectively.

A better understanding of patient's needs leads to better decisions

Today, the point of view of healthcare professionals is not enough to understand your environment. Chronic patients are becoming better informed and are starting to play an active role in everything that concerns their own health.

They express their opinion on health products and services, of which healthcare companies, authorities, payers and professionals are ignorant.
Relying on the study of patients’ real life experiences, via anonymous and aggregated data, Carenity helps healthcare stakeholders in Europe better understand patients’ expectations and habits in order to offer services fully adapted to their needs.

Our MISSION

Transforming patients’ individual experiences into data for researchers and industries in order to stimulate the development of improved offers of care and services

Michael Chekroun, CEO
REAL-WORLD PATIENT INSIGHTS ACCESS to a PANEL OF 210 000 PATIENTS AND CAREGIVERS

5 European countries: France, UK, Germany, Spain and Italy

Our unique SOLUTIONS for REAL LIFE PATIENTS STUDIES

Carenity Monitor

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Carenity Survey

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Carenity Listen

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PatientLive

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Publications

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Patient Barometer

Monitor patients’ perception of your products and the impact of your actions over time

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Ad-hoc on-line surveys

Better understand the needs and habits of patients in real life conditions, in order to support your strategic decisions

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Semantic analysis

Better understand patients’ needs by analysing words they use to describe their health status and treatment

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Quick surveys

Manage your own surveys independently

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Publish the results of your study in order to reinforce your image in the scientific community and with healthcare authorities

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For WHOM?

We accompany more than 50 European and Global partners: pharmaceutical and biotech companies, CROs, and manufacturers of medical devices. We also cooperate with research institutions, consulting companies, communication agencies and healthcare authorities. An increasing number of our partners are researchers, hospitals and public and private universities.

We manage, analyse and publish the results of the studies based on real life patient experience. Our main interlocutors are sales and marketing, market access, medical affairs/R&D teams and public affairs departments.

How can this be APPLIED?

Our studies address various issues which patients and their families are confronted with: perception of a product in real life conditions, difficulties encountered during treatment, factors of non-compliance with treatment, modification or interruption of treatment, impact of the disease and/or the treatment on the quality of life, need for new products or services, participation in clinical trials, out-of-pocket expenses for medical services…

What is the PURPOSE of REAL LIFE PATIENT STUDIES?

1. For Marketing and Market research specialists

Asking for patients’ opinion to identify their expectations in terms of products and services that will improve everyday management of their condition
Helping doctors to better communicate with their patients, by identifying the unmet needs of patients and their caregivers
Improving medical knowledge by sharing patients’ opinions and views via articles, posters and other scientific publications

2. For Market access and Public affairs specialists

Collecting patients’ insights on treatment efficiency and its impact on their quality of life, in order to prepare reimbursment dossiers (under the supervision of a board of experts)
Demonstrating the value of healthcare products as viewed by patients in real life conditions
Encouraging the dialogue between different parties (elected representatives and councillors, healthcare authorities, patients associations representatives, academic societies…), relying on real-life information

3. For medical teams or R&D departments

Involving patients in the process of new product development (unmet medical needs, expected benefits, compliance factors, ...)
Including patients’ opinions in clinical trial design, ensuring the informed consent form is clear and comprehensible, testing other data collection tools, ...
Connecting patients willing to participate in clinical trials with investigators

Our EXPERTISE

  • Over 200 projects since 2011
  • Over 50 clients in Europe
  • A team of Data Scientists, specialised in patient data analysis
  • Management of boards of experts and publication of study results (currently more than 30 publications)
  • Online data gathering: quantitative and qualitative
  • International / multi-countries projects

CONTACT us

To learn more about us or to request a quote please contact us: pro@carenity.com or call +33 (0)1 84 17 42 71.