Lifeline Biotechnologies Inc (LLBO)

[midnightexpress]

they are in the middle of the trials now. If they prove successful they will go for the CE Mark first and then FDA approval. It is faster. They would be able to produce revenue that way in the European market. They need a specific amount of women and need to ask them to volunteer. I would guess they have tested 10 or so but need more, once the other hospital starts joins the trials, which is soon, they would have a larger population of women to draw from and thereby speed up the trial period. It appears to be going as they expected with results and patient numbers.