Our consultative services include:

Study / Clinical Program Planning - Protocol Development

  • Clinical Advisory Groups: drug development, scientific, statistical & trial design consulting
  • Literature review, re-analysis / meta-analysis of reference studies
  • Review and analysis of preclinical studies (toxicity, pk)
  • Analysis in supports of the safety and efficacy sections of IBs
  • Simulation studies
  • Study design, sample size/power calculation, statistical considerations, randomization, including adaptive methods
  • Client representation or support at IND / pre-study regulatory meetings; integrated summary of safety and efficacy analyses - ISSE.

Clinical Trial Oversight

SCiAN's consultants are seasoned professionals with the experience to support you clinical development program. Our senior consultants are available to our Clients to participate in the oversight of clinical development programs as members of clinical / scientific advisory boards or part of your project management team.

We will address your data management and biostatistics needs and recommend the best solution for your study.