Arthur is a biologist and materials engineer and has more than 30 years’ experience in the medical devices industry. Arthur previously served as Director of Devices Registration and Assessment, Director of Postmarket and Director of Biomaterials and Engineering laboratories. He is past Chair of the Regulatory Expert Panel for the Australian industry association AusMedtech and is Special Adviser to the Asian Harmonisation Working Party. He is Visiting Professor at the University of Sydney School of Engineering where he teaches Regulatory affairs.
Chief Executive Officer and Senior Consultant Grant Bennett provides expert consultancy services relating to regulatory compliance in Australia, New Zealand and the Asia Pacific. Grant is also responsible for management oversight of all Australian consulting projects.
Grant joined Brandwood Biomedical in the later part of 2013, bringing with him experience with both the Therapeutics Goods Administration (TGA), along with a multitude of other regulatory authorities throughout Asia.
With over 25 years of experience Sarah’s strengths lie in her strategic approach to market access and the creation of effective reimbursement and health economic strategies. She is expert in preparing complex reimbursement submissions and has assisted many medical technology companies gain market access for innovative technologies and has served on multiple industry committees and is a current member of Ausbiotech and Medical Technology Association of Australia (MTAA).
With over 20 years of regulatory affairs experience, Jeff has extensive experience in the rapidly developing regulatory environment of China. Over the past two decades Jeff has prepared hundreds of successful regulatory submission in a wide area of device technologies. He has an extensive China network, he has conducted many consultations and interactions with China Type Testing Centres and CFDA’s Centre for Medical Device Evaluations and participated with the development of China and international Standards.
With 25+ years of technical manufacturing, operations and regulatory senior management experience in the US and NZ medical device industries, Nancy Yopp provides expertise in regulatory compliance and implementation and commercialization of medical devices, including in-vitro diagnostics. Nancy has worked extensively with animal based products and the risk management associated with these products and has a proven track record working with the varied complexities of both start-ups and multi-national companies.