Expert CRO in clinical research
Pharmaspecific, your CRO in France and internationally for your clinical studies
Pharmaspecific is a CRO based in France that supports pharmaceutical companies, biotechs and medical device manufacturers in running their clinical studies: monitoring, regulatory affairs, on-site coordination, patient expense reimbursement and clinical project management, in France and internationally.
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Clinical studies that are
safer, faster,
and closer to patients
Tailored solutions
Solutions tailored to every stage of your clinical study
Pharmaspecific supports pharmaceutical companies, biotechs and medical device manufacturers with a full range of services: project management, monitoring, on-site coordination, regulatory affairs, GCP compliance audits and patient expense management.
See our services →
Clinical studies that are
safer, faster,
and closer to patients
Our impact in numbers
15+
Years of experience
350+
Studies supported
12+
Therapeutic areas
15+
Countries covered
100+
Investigator sites
12,000+
Patients supported
Phases I-IV
Clinical expertise
98%
Client satisfaction
What do we offer today?
A COMPLETE OFFERING FOR YOUR CLINICAL STUDIES
Pharmaspecific provides sponsors and investigator sites with operational, regulatory and quality expertise that ensures study compliance, reliable data and on-time delivery. Our teams work in France and internationally on Phase I to IV trials as well as observational studies.
Clinical trial monitoring and oversight
Site monitoring and clinical data quality control.
Clinical project coordination
Study management, stakeholder coordination and timeline tracking.
On-site coordination (CRC)
Operational support for investigators and day-to-day study follow-up.
Regulatory affairs
Preparation, submission and follow-up of regulatory files.
Patient expense reimbursement
Secure request processing and full traceability of reimbursements.
Medical writing
Writing and review of scientific and regulatory documents.
Qualified staff provision
Experienced professionals to strengthen your clinical teams.
Clinical research professional training
Hands-on training tailored to clinical research roles.
MAKING CLINICAL STUDY PARTICIPATION EASIER
At Pharmaspecific, we believe the patient experience is a key factor in the success of a clinical study. Our team manages expense reimbursements to make participation easier for patients, reduce logistical burdens and support sponsors' recruitment and retention goals, in line with Good Clinical Practice for clinical trials.
✓ Management of travel, accommodation and meal expenses
✓ Processing and tracking of reimbursement requests
✓ Multilingual patient support
✓ Financial reporting and reconciliation
✓ International reimbursement management
✓ Support for investigator sites
Looking for precise, reliable results?
ENTRUST YOUR
CLINICAL OPERATIONS TO
AN EXPERIENCED CRO
Our experts support you at every stage of your clinical study: regulatory submissions, monitoring, on-site coordination, patient reimbursement management and quality compliance.
Talk to an expert →THEY TRUST US
