WATCH: Quality Issues with mRNA Covid Vaccine Production
Open Science Session by Dr L. Maria Gutschi
"Based on manufacturing standards and lack of basic pharmacological info alone, the product should be recalled" ~ Dr Gutschi
Dr. Gutschi is a pharmacotherapeutic specialist with extensive experience in evidence-based medicine, critical care, antimicrobial therapy, and mentoring and teaching pharmaceutical care. She has been involved in pharmaceutical drug assessment and formulary management, and the preparation of educational materials and research reports for the Canadian Pharmacist Association and for regulatory agencies. She has been employed as a scientific officer for the Patented Medicines Prices Review Board in Canada, and as a clinical pharmacist for the Canadian Forces Health Service Centre, and as a pharmacy consultant for small hospitals to meet multiple accreditation standards.
PANDA’s weekly Open Science Sessions provide an opportunity for science, research and policy to be presented by various leading international experts in a variety of diverse fields. These sessions aim to broaden understanding and inspire new insights.
* Our apologies for the poor sound quality
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What astounds me is that so many medical professionals are coming to these conclusions so desperately late in the day. Where were they, when all of us lay-people were demanding answers two and a half ago?? Sorry. I have genuine credibility issues with the medics who were asleep at the wheel.
P.-H. Lambert, D. M. Ambrosino, S. R. Andersen et al., Consensus summary report for CEPI/BCMarch 12–13, 2020 meeting: Assessment of risk of disease enhancement with COVID-19 vaccines, Vaccine.
"Of course, disadvantages include the novel nature of both mRNA and DNA vaccines without any licensed vaccine with either technology to date and lack of experience for mass production."
Within 9 months of the above, the UK was rolling out industrially scaled up jabs population wide.
My bet is that everything was already quite well in place (CEPI).