Big Pharma is swimming in windfall profits with the global governments paying Pfizer, Moderna J&J, and Astra Zeneca to produce the experiemental mRNA COVID injections…that in turn are causes new and aggressive diseases that Big Pharma provides more of their high profit drugs to treat symptoms by every body part…that in turn make us all sicker and more burdened with side effects and complications…which in turn include aggressive, novel, stage 4 deadly “Turbo Cancers” that do not respond to traditional treatments. VOILA! Big Pharma to the “rescue” yet again…set to make trillions in profits this time from mRNA-based gene therapy “vaccines” for the tsunami of turbo cancers expected to rise dramatically again in 2025. Johnson & Johnson announced plans to shell out $2 billion to acquire the drug developer “Ambrx Biopharma” to treat Turbo Cancers with same unproven technology as Pfizer is launching with its $43 billion Seagen acquisition. Both expect to once again bring in windfall profits to provide “treatments” for diseases their own experimental COVID injections caused in the first place. Canadian oncologist and researcher discussed these plans, and the dangers, in more detail here: https://makismd.substack.com/p/johnson-and-johnson-to-acquire-2?utm_source=post-email-title&publication_id=1385328&post_id=140761669&utm_campaign=email-post-title&isFreemail=false&r=ohbu8&utm_medium=email
Today’s Inside Pharma Whistleblower Report experts discuss the dangers of the mRNA technology and the flagrant and illegals use of taxpayer funds in the UK to build these manufacturing facilities in the middle of small residential neighborhoods without any preliminary study of the human and wildlife health hazards and environmental risks of bringing in these biological materials without any regulatory oversight. The British government, Big Pharma, and WEF working together using taxpayer money and Big Pharma profits appear determined by any means possible to get mRNA and foreign DNA into human beings and all animals – domestic pets, food animals, and wildlife.
Read more in this linked PDF from our Pharma expert on the deadly dangers of gene therapy products:
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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 Biologics for 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
