Megan W. is a seasoned professional with extensive experience in regulatory affairs within the medical device sector. Currently serving as the Director of Regulatory Affairs at AirLife since June 2023, Megan has held various regulatory positions including Regulatory Affairs Manager at Vyaire Medical and LivaNova. Previous roles include Principal Regulatory Affairs Specialist at Philips, where responsibilities included preparing FDA submissions for Artificial Intelligence and ultrasound devices. With a foundation in regulatory compliance from roles at Philips Respironics and DeVilbiss Healthcare, Megan possesses a strong track record of ensuring medical device compliance across multiple markets, including the US and EU. Megan holds a Master of Business Administration from California University of Pennsylvania and a Bachelor of Science from Indiana University of Pennsylvania.
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