By Strategic Area

Clinical Services

For biotech and pharmaceutical companies, medical device manufacturers, non-profit organizations, and academic institutions looking for a comprehensive overview of We4CR’s clinical expertise across all phases of a study.

The services described here span the entire study lifecycle. For phase-by-phase details, see the dedicated pages on Study Set-up, Start-up, Study Conduct, and Study Close-out.

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Study project management

We coordinate your study end to end, from protocol to close-out, as a single point of contact between sponsor, sites and vendors.

Data management and biostatistics

We manage the collection, cleaning and analysis of data throughout the study, with remote verification of data entry and periodic quality analyses.

Clinical monitoring (CRA)

We monitor the study in a centralized, risk-based way, with remote or on-site visits where risk requires it, to verify adherence to the protocol and data quality.

Site selection and site management

We select the sites best suited to your study through feasibility questionnaires and manage the relationship with them throughout the study.

Pharmacovigilance and safety

We manage adverse events, serious adverse events and device deficiencies and the related reports to authorities and ethics committees, with the review of our Medical Director.

Medical writing

We draft protocols, synopses, information sheets and informed consent forms, Clinical Study Reports and scientific publications.