What is We4CR?
We are a CRO - Contract Research Organization
specialized in innovative solutions and research services to satisfy the needs of the Biotech, Medical Devices Industries,
Non-profit Organization as well as Academic Institution
WE4CR allows you to conduct studies by integrating the best Innovations in the field of Clinical Reseach by making the Study more "Patient Centric"and with the most cutting edges Technologies that allow to conduct properly a study
ePRO & PROM
Best tools to capture, store and process data, to report life quality, daily functioning, symptoms, and other aspects of health and well-being
eTMF & Repository
Best eTMF and Repository compliant with GDPR and data protection
eCRF & EDC
Best cutting edge solutions for EDC selected for your needs
Wearable Medical Devices
Best wearable technology in healthcare to monitor patient’s vital signes in a smart way
We4CR main therapeutic areas
CAD
Coronary Artery Disease
Blockages in heart arteries which happens when plaque builds up on the inner walls of your coronary arteries.
PAD
Peripheral Artery Disease
The diseases of the blood vessels in areas outside the heart, the ones that affects the arteries that carry blood to the legs and arms.
PSYCHOLOGY
Clinical Psychology is a psychological speciality concerned with the assessment and treatment of mental illness, atypical behavior, and psychiatric problems.
NUTRITION
The field that establish the required nutritional needs that best support survival, growth, and development in subpopulations.
What We4CR does?
We4CR provides Consultancy and Clinical Research services to design, manage and conduct your Clinical Studies by guaranteeing professional approach, monitored results, respect of GCP, Data protection and compliance with local law.
The main Services of We4CR are:
- clinical trial setup
- start-up
- protocols drafts
- medical writing
- clinical trials management
- data management
- statistical analysis
- monitoring
- site management
- technical support
What We4CR does in every step of a clinical study?
SET-UP
In the preparatory phase of a clinical trial We4CR carries out all the analysis and design activities needed to start the study, from the drafting protocol and the sinopsys - including the selection of stakeholders to be involved and the stipulation of insurance - up to the recording on clinicaltrials.gov
START-UP
We4CR prepares and collects all the documents needed to start the clinical trial (TMF, IFS, Dossier to submit to EC/CA, ...) until the mandatory approval or notification
STUDY DEVELOPMENT
We4CR supports you in Data Management (including monitoring and checking conformity to ICH-GCP and relevant legislation) and Data Entry.
STUDY CONCLUSION
We4CR notifies to Competent Authority (CA) and Ethics Committee (EC) the End Of the Study (EOS). We4CR is in charge from the notification of the end of the study to the Database Lock (DBL), including Clinical Study Report (CSR), statistical analysis, and Data Cleaning.