Virtual Classroom Training

Bespoke interactive e-learning

This extensive training on validation will provide deep insights into regulatory requirements, introduction in statistics, computational details, and all-in-one designs of experiments. Register and learn from the knowledge of our expert Eric Rozet.

Type: Virtual Classroom Training

Duration: 2 Days (each divided into two 0.5-day sessions)

Who should attend?: Assay research Scientist, Validation QC Manager

Extensive training to maximize the chance of successful validation of bioassays. The training will cover the following topics:

  • Regulatory Requirements
  • Introduction in Statistics
  • Computational details
  • All-in-one designs of experiments

Eric Rozet 

Eric Rozet is Director Statistics at PharmaLex Belgium company in Louvain-la-Neuve (Belgium). He has experience of more than 15 years in pre-clinical, non-clinical statistics, and CMC in particular in statistical aspects related to (bio)assays and (bio)processes development, optimization, validation, transfers. He trains statisticians and analysts of the Bio-Pharmaceutical Industry on topics such as optimization, validation, robustness, and transfer of analytical methods and processes. Eric also trains Statistician in Bayesian modeling and Designs of Experiments. He is also the author of more than 100 articles and book chapters in applied statistics and is regularly giving conferences on these subjects. Eric has a B.Sc. degree in Bio-engineering, a Master’s degree in Biostatistics, and a Ph.D. degree in Pharmaceutical Sciences. 

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