moosey and others, tbh, this is why I am a bit confused over the HK presentation which put the Hermia product ahead of the Breast product. I would have thought because of the risks involved, there would be a need for extensive clinical trials and FDA/CE approval before this product got anything like broad acceptance in the medical community (and in fact, given the J&J experience, PNV would be quite silly to get ahead of themselves in this for fear of a massive class action).
The stated aim of having a Hernia product in the market in 2019 doesn't ring true to me. I am hoping for some clarity in the half-yearly. This has certainly been a worthwhile discussion.
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