Hi All,
I'm a Quality and Regulatory Affairs Manager in a MedTech company developing SaMD. Given that it is still a fairly new area in the medical device field, I find myself facing a number of challenges. As a result, I have set up a Software as a Medical Device (SaMD) focus group on Linkedin -
https://www.linkedin.com/groups/13992526/This is a niche community only for Quality and Regulatory Affairs professionals and medical device software developer who are interested in learning more about the challenges, trends and current regulatory topics related to SaMD *and* sharing their experiences.I would like to invite anyone who is interested and I look forward to learning from each and every one of you and sharing my experiences. Thank you!P.S. If you have any questions, please feel free to reach out anytime!------------------------------
Yan Chia
QARA Manager
Australia
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