Expert Biostatistician Shocking Exposé of Pfizer/BioNTech Clinical Trial Malfeasance

French expert pharmaceutical Biostatistician, Christine Cotton, discusses her detailed analysis of the VAERS vaccine adverse effect raw data with Pharma expert Hedley Rees and US physician Dr. Vliet.

The results of her analysis of the procedural and regulatory steps taken to introduce COVID-19 emergency vaccines led Christine to conclude that COVID-19 vaccines carry significant health risks to all members of the public, be they children, grown adults, or the elderly. Within this cross-section of society, additional risks are identifiable for pregnant women and their babies.

The risks deserve special attention because of the massive damage happening around the world with life-changing disabilities, staggering declines in live birth rates in highly vaccinated countries, catastrophic rates of sudden deaths in young, healthy people, and rising autoimmune diseases and deadly cancers.

For more on Christine’s extensive report and the 2020 article mentioned in today’s show, go to https://www.truthforhealth.org/2023/07/expert-biostatistician-shocking-expose-of-pfizer-biontech-clinical-trial-malfeasance/; https://christinecotton.com/english_presentation https://www.nejm.org/doi/suppl/10.1056/NEJMoa2034577/suppl_file/nejmoa2034577_protocol.pdf.

Our Guest today: Christine Cotton, French Biostatistician with 23 years of experience in the pharmaceutical industry and CEO of a CRO Clinical Research Organization. Her website is www.ChristineCotton.com. Follow Christine on Twitter @StatChrisCotton.

Hedley Rees, based in the United Kingdom. Mr. Rees has been providing consultancy on developing, manufacturing, and distributing drugs that are fully compliant with the GMP requirements of 21 CFR Title 21 since 2005 through his company, PharmaFlow. Before that, he spent 16 years in senior roles in Big Pharma (Bayer) and ten 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 Biologics for Wiley, NJ 2011. His expertise is in anything to do with manufacturing 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.

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 the fight for medical freedom on all fronts.

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