Hey @RuddeOne@Rod_Valens or @more4less or anyone who has attended AGM or talked to Yacov during presso is in a better position to answer you
Thanks RV & m4l.
G.
Here is my version:
GMPatch
has been approved by CE, and is still waiting for FDA & CFDA clearances; submitted late last year(?)
Primza
Next steps:
1.Official "clearance" document for mfg facility expected in 3 weeks (frm 29/10) is received.
1a Primza is approved for sale in China
2.Yacov to ratify all MOUs (last few weeks and next few weeks)
3.Productions can start for Primzas
4.For USA,
Winola MOU is conditional on Yacov getting FDA GMPatch in addition to Primza clearance.
4a. However whether Gmed can do direct Primza sales to retail buyers via GmedDX (cardostaff & Telei) in another matter(?)
All i can say is Yacov's methodical and meticulous laying the foundation - one brick at a time to make Gmed a global & household name is unfolding before our very eyes.
Its a privilege to be part of his journey.
LTHs will be Big Winners!
aimo
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