• Global experts backed by cost-effective and scalable teams 
  • Ability to maintain alignment with your team and adapt to your operational oversight requirements 
  • Proven expertise in small to midsize environments across pharma, biotech, and medical device 
  • Expert analysis to pave a smoother path from trial to submission

We offer rapid onboarding and hands-on support across statistical programming, clinical data management, and biostatistics services. Statistical programming includes end-to-end support for regulatory-ready deliverables from SDTM and ADaM development to TLF generation, executed in compliance with evolving standards. Clinical data management services span study startup to database lock, combining speed, quality, and familiarity with EDC platforms like RAVE and Veeva. Biostatistics support includes protocol input, statistical analysis planning, and final output review, tailored to meet submission expectations. 

Experience the EPHICACY EFFECT