Real-world experience in support of clinical research
Every clinical study presents specific scientific, regulatory and operational challenges. For more than 15 years, Pharmaspecific has supported sponsors, biotechs, medical device manufacturers and investigator sites in implementing solutions tailored to their challenges.
Discover through our clinical research case studies how our teams have contributed to the success of clinical research projects across various therapeutic areas and operational contexts. These clinical research experiences illustrate our ability to meet the specific needs of each project and to support all clinical research stakeholders.
Explore our clinical case studies
- Oncology
- Haematology
- Virology
- Rare diseases
- Cardiology
- Medical devices
Supporting a multicentre oncology study
Setting up patient expense management and coordinating investigator sites for an international study.
- Multicentre observational study on optimising the oncology care pathway.
- Phase II clinical trial (paediatric oncology) — CINV prevention
- Phase II clinical trial in thoracic oncology in a targeted population with a rare molecular alteration
- National real-world data (RWD) centralisation project in oncology
Strengthening monitoring for an international trial
A dedicated CRA team to ensure data quality across several countries
- Multicentre Phase III trial in patients with relapsed multiple myeloma
- International Phase III clinical trial comparing a new molecule combined with rituximab with standard treatment in lymphomas.
- Bioequivalence clinical study in haematology in around twenty patients, comparing a new generic with the reference molecule
Securing the launch of a vaccine trial
Coordinated regulatory submissions in 6 countries simultaneously
Facilitating recruitment for an orphan disease
A patient concierge service to reduce the burden on a geographically dispersed population
Preparing for a regulatory inspection with confidence
An independent GCP audit to anticipate deviations before inspection
Bringing an implantable device into MDR compliance
Comprehensive regulatory support, from strategy to submission
LET’S TALK ABOUT YOUR PROJECT
Would you like to discuss the challenges of your next clinical study with our experts?