Half the posters were screaming for a status report last week. IMO it touched on many very important topics, perhaps the most important being KFDA status.
Illuminator, I agree with you for the most part, this was a feel good PR with alot of info everyone should have already been able to figure out if they believe.
However, I think there was one major piece of info that takes this from a FLUFF PR to a SOLID NEWS PR; everyone wants to see KFDA approval and now we have a deadline:
"3. Amend our KFDA application with the adjustments made to the device and software. Expected approval is within six-eight weeks for anticipated sales in South Korea"
Only somebody who has not read this board and or the yahoo board could post something like you just did imho. It removed the doubts from almost every piece of misleading info naysayers had posted.
You do understand you can't go into production without a finalized product. Now that they have a finalized design it won't take very long for them to start banging out BioHarps left and right imho.
Finalize the end product design relating to the device and software. This has already been agreed upon by management and we will look to have the finished product very shortly