I don't know who this lady is, and I don't even know the assumptions on which she is based. All I know is that everything that has happened in the last 3 years could not happen without the blessing and total all in of the worldwide military. The fish stinks from the head and they drop little " crucial" other slices of smelly leftovers on us. In any case, let it be known, my kitchen is updated to biosafe level type 4 lab. Military, don't be shy!
I hadn’t “heard” of her before, either.
I took a bit of time this morning and read several of her essays on this link, and I must say, her comments, statements and observations are based on far more than “assumptions”.
Here is a snippet from her background:
“I am an ex-pharmaceutical research and development (R&D) industry executive and entrepreneur. I spent 25 years working in the industry in various roles, countries and ultimately managing my own companies. I worked initially as an econometrics and management consultant, and later as clinical trials contractor for 60+ pharmas, large and small. My clients included Pfizer, Johnson & Johnson, Novartis, AstraZeneca, GSK, and many smaller biotechs. I worked with “channel partners” such as large contract research organizations (CROs) - Parexel, PPD, ICON, and others. I interacted with the FDA and other regulators on behalf of my clients, and as a member of Cardiovascular Safety Research Consortium on subjects related to assessments of cardiovascular safety of new drugs in clinical trials. Around that time, I met Robert Califf who is now the Commissioner of the FDA. He was my business competitor and was running rather poor quality cardiac safety trials for pharma at an academic lab at Duke University. There is a thin line between “poor quality” and “fraud” in clinical trials, but we will return to this topic.”
For what it’s worth, I highly recommend reading everything she has written.