The VERDICT is in. Covid shots have no evidence of safety OR effectiveness, as meticulously documented in the international expert WITNESS STATEMENT OF Dr. Pedro Morago from the UK, which concludes: “From the data available, there is no sufficient evidence that FDA and MHRA have conducted a rigorous, critical appraisal of the evidence of efficacy/effectiveness and safety of COVID-19 vaccines with explicit reference to the key criteria of External Validity, Internal Validity and Reliability. After a rigorous, critical appraisal of the evidence of efficacy/effectiveness and safety of COVID-19 vaccines with reference to the key criteria of External Validity, Internal Validity and Reliability, it can be concluded that the value of such evidence is not strong enough as the basis for a large-scale implementation of the intervention, and not methodologically acceptable as the basis for mandatory vaccination.”
Our guest on today’s show is Pedro Morago, Ph.D, expert in evidence-based research methods, at Teesside University, Middlesborough, England. For more on Dr. Morago’s background, click here: Pedro Morago Publications, Teesside University · Advanced Clinical Practice
For more information go to Truth for Health Foundation website www.TruthForHealth.org. Download our Vaccine Injury Treatment Guide, file a Citizens Vaccine Injury Report, check our medical and legal resources for help, sign up for newsletter alerts and join in the fight for medical freedom on all fronts.
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HOST BACKGROUND AND WEBSITE RESOURCES:
Hedley Rees, based in the United Kingdom. Mr. Rees has been providing consultancy on the development, manufacture and distribution of drugs that are fully compliant with the GMP requirements of 21 CFR Title 21, since 2005 through his company, PharmaFlow. Prior to that, he spent 16 years in senior roles in Big Pharma (Bayer) and 10 years in biotech (British Biotech, Vernalis and OSI Pharmaceuticals (now Astellas). Mr. Rees also authored Supply Chain Management in the Drug Industry: Delivering Patient Value for Pharmaceuticals and Biologicsfor Wiley, NJ in 2011. His expertise is in the area of anything to do with manufacture through the three phases of clinical trials (and preclinical if required) and ongoing distribution of the commercial supply. Where regulations have been breached, he has a duty to bring this to the attention of regulators, as has been happening with the frozen vials of COVID shots that were shipped only part way finished.
Hedley joins Truth for Health Foundation Team: https://open.substack.com/pub/hedleyrees/p/hedley-joins-truth-for-health-foundation?r=xoehy&utm_campaign=post&utm_medium=web
Follow Hedley Rees on his Substack column, INSIDE PHARMA, where he shares all he can to expose the lies and deceptions that are costing lives and jeopardizing public safety. Watch one of his many interviews here: https://rumble.com/v14gou4-drug-development-expert-sounds-alarm-over-rushed-to-market-covid-19-vaccine.html
Read more on Facts about SARS-CoV-2 Injections (aka DNA vaccines) and advanced therapy medicinal products (ATMPs): https://open.substack.com/pub/hedleyrees/p/facts-about-sars-cov-2-injections?r=xoehy&utm_campaign=post&utm_medium=web Watch Recent interview discussing the violations of manufacturing processes and regulations that are supposed to keep us safe: https://rumble.com/v1qe9nk-freeman-interviews-hedley.html