L. Vromans, PhD

Zwiers Regulatory Consultancy

Speaker Module C

Lisette currently holds the position of Senior Consultant at Zwiers Regulatory Consultancy. She previously worked for Organon (which she joined in 1986) and worked as a Regulatory Affairs Scientist, participating in the early and late development and subsequent world-wide regulatory filings of products in the areas of contraception and neurosciences. She joined MSD through the respective mergers with Schering-Plough (2006) and Merck (2009).

In her various roles, Lisette has been responsible for advising product development teams or pharmaceutical companies on regulatory requirements and procedures, proactively identifying critical Regulatory Policy issues and recognizing regulatory obstacles for drug discovery and development and to work with Regulatory Agencies and Industry Organizations such as IFPMA, EBE, EuropaBio, EFPIA and EVM to eliminate these obstacles.

She likes to share her experience by giving training and workshops (e.g. EuroDIA, Medicademy, Uppsala Monitoring Centre and University of Groningen)

Lisette studied HLO Biochemistry