We offer a full menu of biostatistical services for any part, or all, of your clinical trial. Our à la carte approach allows sponsors to select areas that need to be bolstered with our expertise in biostatistics. Simply choose what you want, or even customize it to fit your needs. Our approach provides an opportunity for clients to get a taste of what working with K3 is like.




K3-Innovations has a team of biostatisticians with years of industry experience to fulfill any requirements you might have. From phase I to IV, through protocols and developing/reviewing SAPs, our biostatisticians have you covered regardless of therapeutic areas. Our team stays up to date with all the regulatory requirements and practices to ensure the integrity of your clinical trials. With the help of Bayesian methods, biomarkers data analysis, and biostatistical analysis, we help you stay ahead of your projected timeline, reduce your risks, and help bring your product to market in a cost-effective manner.


  • Real-world evidence (RWE), Registries,
    clinical trial, Pre-clinical, etc

  • Protocol development

  • Determining primary and secondary endpoints

  • Sample size calculation

  • Statistical Analysis Plan

  • Development/planning of analysis methods

  • Statistical Modeling

  • Regulator precedent review

  • ISS and ISE Statistical Analysis Plan
    for NDA/BLA submissions

  • Ad-hoc analyses/Publications/Presentations


Get in touch with us today and let us know how we can help you