If elected, it would be a privilege to further contribute, based on my experience from:
• academia (PhD and post-doc in drug delivery)
• regulatory agency (MHRA: 18 years working with medicines and medical devices)
• medical devices industry (small MD companies and MedTech SPIN steering group)
• medicinal products industry (co-authoring EBE/EFPIA reflection papers on regulation of combination products; attending key international conferences on quality issues for current and emerging medicinal products and technologies)
I have a passion and enthusiasm to bring people from different backgrounds together - for sharing experiences, understanding different perspectives and collaborative working towards appropriate, risk-based and pragmatic regulatory solutions.