4Pharma provides high-quality, cost-effective solutions to ensure the successful management and delivery of clinical trial data in accordance with your timelines and budget. We provide you with state-of-art biostatistics services by highly experienced pharma professionals to support you in these processes. The exceptional pharma experience of our staff enables us to act in senior roles within (bio)pharma companies or providing statistics for single studies, clinical or non-clinical.

Services in statistics, including:

  • Study design and sample size calculation
  • Statistical programming, analyses and reporting
  • Bioinformatics
  • Epidemiology
  • Tailored training in statistics
  • Consultation on any level

Key Competitive Advantages

4Pharma has accumulated vast experience in several therapeutic areas including oncology, neurology (especially PD), ophthalmology, musculoskeletal, respiratory diseases, pharmacology, infectious diseases and gynecology. 4Pharma people have played a key role in successful global regulatory submissions by taking responsibility for statistics, data management, and preparation of the (electronic) dossier. Consequently, these people have participated in numerous face-to-face meetings with the FDA (USA), EMEA and national authorities (Europe), and PMDA (Japan). Currently, 4Pharma plays a key role in several drug development projects aiming at regulatory submissions. With our approach of being involved and contributing to the drug development process instead of being an external “number team” and with our experience and great track record we truly believe that using our statistical services will benefit the customers and their compounds in the way forward towards the market.