hedley lease We draw on 35 years of supply chain experience to explain the real “big pharma system.” He made it clear that the MHRA was just an organization. A large number of staff have left the company since 2016, but who will replace them?
Indeed, yes Anyone Or is the MHRA run by largely unqualified and inexperienced personnel trying to give the impression that it cares about our safety?
What is the MHRA that no longer considers itself a regulator but an enabler? An enabler for the same big pharma companies?
Vaccines typically take five to 10 years, or even up to several decades, to produce, depending on the complexity of the disease and situation. Novel coronavirus infection (Covid-19) novel “Vaccines” fell slightly below 1 year. But how do new “vaccines” and new drugs like paxlobid and molnupiravir get to us?
UK Column was delighted to have the opportunity to speak to Hedley Rees, Managing Consultant at PharmaFlow Limited, a UK consultancy specializing in life sciences operations and supply chain management. He has over 35 years' experience in industrial engineering, logistics and supply chain management, having previously held senior positions at Bayer UK and British Biotech.
He explains how a simple molecule goes through the process of becoming a drug in a cupboard, through several rounds of testing, testing, retesting, and retesting before it reaches pharmacists and doctors. We will talk in detail about the hurdles and obstacles to overcome.
We learned from him that all medicines must undergo rigorous testing. all prior to final submission to the FDA, MHRA, or other applicable regulatory authority. approval. The estimated duration is 11 years. Any It takes time for drugs to reach humans, and many fail along the way and are even rejected at the final stage. It's a very expensive and time-consuming process, so it's understandable how drug companies would want to cut corners. But at what cost to us?
According to Bill Gates at the World Economic Forum's CEPI launch conference in 2017, safety and manufacturing work can be “reduced.” Hear it for yourself at this timestamp. Clearly, what Gates predicted five years ago is exactly what Hedley Rees is observing within his own industry. He describes the arduous journey of some of our best-known medicines, transforming them into new and fragile experimental drugs that we now know as COVID-19 “vaccines.” Contrast this with the rapid rollout of injectable drugs.
Following discussions at the G7 Health Ministers' Meeting, hosted by the UK Government as part of its G7 Presidency, the UK Government and industry leaders have set out a plan to develop and introduce high quality diagnostics, therapeutics and vaccines within just 100 days. We agreed to work toward this goal. Regarding the identification of a “new pandemic threat.”
of 100 days mission It was devised by Melinda Gates and Sir Patrick Vallance to give us all “shortcuts” to medicines and vaccines with little or no safety research.
Among Hedley Rees' many books, Tame the giant pharmaceutical monster.
Click here for the subsequent UK column interview with Hedley Rees.
