Arthur Noach obtained an MSc in Pharmacy and a PhD in pharmacology/pharmacokinetics from Leiden University and a PharmD from Utrecht University. He has over 25 years of experience in the pharmaceutical industry. He worked at Organon pharmaceutical company as a scientist, and for more than 24 years he has been a senior consultant for the nonclinical development of drug candidates at Venn. His experience is in designing nonclinical study packages required before starting clinical studies and beyond up to product registration, based on international guidelines for either small molecules or biologics and vaccines. Arthur’s work also includes consulting on the set-up of studies, monitoring contract labs and reviewing study reports. He has vast experience in writing nonclinical parts of briefing books, Investigator’s Brochures and IND modules (eCTD format). Furthermore, he acts as consultant and principal investigator for pharmacokinetic and toxicokinetic studies performed at Venn, both non-GLP and GLP.