• 01 Dec 2020

    PSI ToxSIG Webinar: Combining Sexes

    The webinar will provide a general introduction to the topic of combining sexes for statistical analysis in Toxicology. It will also discuss guideline recommendations pertaining to this topic.
  • 02 Dec 2020

    PSI Webinar: Risk Based Monitoring & QTL's

    Since the introductio of ICH-E6 R2 Addendum sponsors must introduce formal Quality Risk Management and define Quality Tolerance Limits to their clnical development programs. This webinar will cover an introduction to those concepts, recent developments and examples of how companies are defining QTL's in practice.
  • 08 Dec 2020

    PSI Webinar: Innovative approaches in the development of pediatric medicines

    Do you want to learn more about innovative approaches for the development of pediatric medicines? Then join this PSI webinar on December 8. We have organized an exciting webinar with very knowledgeable speakers who will share their thoughts, ideas and experiences, including case studies, on a range of issues relating to historical data, Bayesian methodology, and partial and full extrapolation approaches in the context of developing pediatric medicines.
  • 10 Dec 2020

    PSI Vaccine SIG Webinar: Some considerations on developing COVID-19 Vaccines

    Statistical Observations on SARS-CoV-2 & Crisis Vaccine Clinical Testing. Scott Patterson, Bo Fu, Ya Meng, Fabrice Bailleux, Josh Chen.
  • 12 Jan 2021

    PSI EIWG Webinar: PIONEERing estimands in Clinical Research

    Bringing estimands to life through a real case study. Members of the estimands Implementation Working Group (EIWG) will describe the background and study objectives, intercurrent events of interest and chosen estimands in the PIONEER study.

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