She will provide strategic advice and scientific leadership to support clients in clinical development, registration strategy, submission, early post-approval strategy
Chantal van Gils NDA, MD, Ph.D., specialist in epidemiological analyses and outcome research joins the NDA Advisory Board as Director of Epidemiology and Real-World Evidence.
In this role, she will provide strategic advice and scientific leadership to support clients in clinical development, registration strategy, submission, early post-approval strategy or other health authority interactions for high priority programs and/or non-interventional studies across all therapeutics areas, and notably oncology and ATMP.
Kurt Stoeckli, President of NDA Advisory Board, said: “I am excited to have Chantal join the NDA Advisory board. I am convinced that she will bring profound knowledge in this emerging area, combined with practical experience and contextual judgement. She will be able to help clients come up with the best global strategy to get innovative medicines the fastest and safest way to the patients in need.”
Chantal said: “With the trend towards precision medicine, regulators have discovered the value of ‘real-world’ data to supplement clinical research for benefit/risk assessment. As an epidemiologist with extensive experience in real-world research, I am excited about this trend and even more about the opportunity to be part of the NDA team, working together with my colleagues at NDA to support clients to develop tailor-made evidence strategies to meet challenging regulatory requirements.”
Johan Strömquist, CEO of NDA Group, said: “The NDA Advisory Board is one of a kind – no other professional body comes as close to reflecting the current opinions and practices of the world’s regulatory and reimbursement agencies. I am delighted to welcome Chantal to our team. I very much look forward to working with her to help bring more good medicines to people all over the world.”
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