Regulatory gun for support
Hey there. I'm an experienced regulatory affairs consultant, over 15 years in medical devices with the last 8 years at a globally renowned consultancy. I've supported companies across a range of device types and classes, from startups to Fortune 500 companies. My experience is primarily in EU CE marking and US FDA but also have global market access expertise. I'd be very interested to now hear from early stage start ups or solo entrepreneurs looking for regulatory advice or commercialisation strategy, and provide some guidance where I can. This would be free but isn't totally altruistic, as I'm hoping to make a lateral shift into the start up advisory space and am trying get a better idea of the types of questions and challenges you have, so this could potentially be beneficial for both of us! Thanks in advance.