Inside Pharma Report: Bill Gates Mastermind Behind Capturing Global Health Regulatory Agencies?

Is Bill Gates the mastermind using his close ties with the UK government Ministers and King Charles to capture and control the UK regulatory agencies overseeing medicines and vaccines to collect massive profits and continue his depopulation agenda?

Has he succeeded in setting up a new and parallel regulatory agency under his control to push out even more experimental gene therapy agents without oversight by the UK Parliament?

Evidence is mounting that this is the case as our Whistleblowers –Hedley Rees from the UK and international attorney Dr. Reiner Fuellmich—discuss today with US physician Dr. Vliet. Inside Pharma host Hedley Rees also exposes the surreptitious steps the Medicines and Health Products Regulatory Agency (MHRA) has taken to change its Regulations to allow gene therapies, and other advanced medicinal products, to be manufactured without the safety umbrella of there being a proper Quality Management System in place. Read more here: Subject: FOI Request—substantial change in 2022 edition of Rules and Guidance for Pharmaceutical Manufacturers and Distributors: PART IV “Guidelines on Good Manufacturing Practice Specific to Advanced Therapy Medicinal Products (ATMPs)

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 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 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

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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