Sure TILLI,
From: Annex 7 of COUNCIL DIRECTIVE of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices (90/385/EEC)
"2.3.1. Clinical investigations shall be performed according to an appropriate
state of the art plan of investigation defined in such a way as to
confirm or refute the manufacturer's claims for the device; the investigations
shall include an adequate number of observations to guarantee the
scientific validity of the conclusions."
http://ec.europa.eu/growth/single-m...ards/implantable-medical-devices/index_en.htm
My best wishes to Oncosil and the team to cover all those points. I think they may have knocked over one of the "non-essential" requirements. ("key requirement"...LMAO... they need to sack their advisor)
Where do I short? can I sell your shares, I'll give them back to you.
Why am I so negative on Oncosil? well TILLI, my base nature is in the scientific and academic arena... and I openly despise companies that openly bullshit their way through life.
top pick in health sector, page-5
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