Studies&Me
Studies&Me is Europe's first virtual contract research organization dedicated to transforming clinical research through digitalization and patient engagement. Their mission is to set new standards in treatment development by providing end-to-end solutions that include mobile app design, project management, patient recruitment, data management, and regulatory compliance. They focus on personalized treatment development, increasing diversity in trials, and enhancing participant experience, aiming to deliver superior clinical outcomes with a patient-centric approach.
Industries
Nr. of Employees
small (1-50)
Studies&Me
Denmark, South Carolina, United States, North America
Products
Decentralized pilot study for type 2 diabetes monitoring
A decentralized pilot evaluating remote blood glucose and behaviometric monitoring in people with type 2 diabetes.
Decentralized genetic association study in atopic dermatitis
A decentralized clinical study investigating how genetic variation relates to atopic dermatitis outcomes.
Combined early-phase interventional decentralized study for topical treatment
A combined phase 1/2a interventional study executed in a decentralized format to evaluate a topical investigational treatment for precancerous skin lesions.
Decentralized pilot study for type 2 diabetes monitoring
A decentralized pilot evaluating remote blood glucose and behaviometric monitoring in people with type 2 diabetes.
Decentralized genetic association study in atopic dermatitis
A decentralized clinical study investigating how genetic variation relates to atopic dermatitis outcomes.
Combined early-phase interventional decentralized study for topical treatment
A combined phase 1/2a interventional study executed in a decentralized format to evaluate a topical investigational treatment for precancerous skin lesions.
Services
Design and develop participant-facing mobile applications for data collection, task management and engagement.
End-to-end clinical trial project management covering study setup, execution and close-out.
Develop study protocols and prepare regulatory submission documents.
Recruit participants using combined online/offline channels and partnerships with patient communities.
Identify and engage clinicians for investigator roles and provide digital tools to support site performance.
Pre-screen participants using a mix of remote assessments and on-site checks to confirm eligibility.
Design and develop participant-facing mobile applications for data collection, task management and engagement.
End-to-end clinical trial project management covering study setup, execution and close-out.
Develop study protocols and prepare regulatory submission documents.
Recruit participants using combined online/offline channels and partnerships with patient communities.
Identify and engage clinicians for investigator roles and provide digital tools to support site performance.
Pre-screen participants using a mix of remote assessments and on-site checks to confirm eligibility.
Expertise Areas
- Decentralized and hybrid clinical trial management
- Patient-centric study design and co-creation
- Digital health platform development and UX for studies
- Remote physiological and behaviometric monitoring
Key Technologies
- Mobile study applications
- Electronic informed consent (eConsent)
- Electronic patient-reported outcomes (ePRO)
- Remote physiological monitoring