UK Medicines Control Agency (MCA) renamed in 2003 the Medicines and Health Care products Regulatory Agency (MHRA)
Allopathic Inc 

[UK FDA. The MCA became The Medicines and Health Care Regulatory Agency (MHCRA) and in 2005 the CSM became the Commission on Human Medicines.]

See: Committee on Safety of Medicines (CSM) Medical Research Council 

SeeFDA Vaccine Conflict of Interest quotes ACIP: The Advisory Committee on Immunizations Practices  Joint Committee on Vaccination and Immunisation

Committees: The Independent Review Panel for Advertising (IRPA) and the Independent Review Panel for Borderline Products (IRPBP).

[2016 April vid] PLEASE SHARE!!! This COURAGEOUS Woman Needs Our Support  Amanda Mary Jewell is under fire from the MHRA for allegedly selling vitamin B17 in the form of apple seeds or apricot kernels. She is being charged with several offences and the MHRA is trying to make an example of her holistic methods and knowledge. *** Let it be known that there is NO payment options on the website so there are technically NO products for sale. She is being assaulted for claiming that B17 fights cancer. It does, and she is merely stating a fact. They (The MHRA) have to understand that the truth about an important vitamin must become public knowledge and the charges against her are unfounded and only in place in order to make an example of her to other holistic practitioners. A court proceeding will take place in the United Kingdom, and Mary will be unable to attend as she is not in the country. A judge will make a decision and we have predicted that the proverbial book will be thrown at her. The MHRA needs to back off and they need to back off now. If they do not, they are admitting to backing up an evil empire of conglomerate medicine and supporting an industry KILLING MILLIONS IN PLAIN SIGHT. They are supporting the wrong people. PERIOD. Laetrile

[2015 May] Tens of thousands of teenage girls believed to have fallen ill with debilitating illnesses after routine HPV cervical cancer jab   Medicines and Healthcare Products Regulatory Agency had 8,228 adverse reaction reports in 10 years - only estimated 10 per cent of real tally.  Side effects including chest and abdominal pains, exhaustion, breathing difficulties, fibromyalgia and postural orthostatic tachycardia syndrome.  Some have been left wheelchair-bound by apparent effects of vaccine.  Despite this MHRA said it had no concerns on numbers of HPV complaints

[2012 Oct] Secret Papers Reveal Funding Refused to Researchers Looking Into Link Between Chronic Fatigue Syndrome and Vaccinations By Christina England  Although Jones appeared to supply the MRC with sufficient documented evidence for funding to be granted, she was turned down in favor of other research projects that supplied less evidence to support their application.  At the time of her application, ME/CFS was being portrayed as a psychiatric disorder and Jones wished to dispel this myth, proving that ME/CFS was in fact a physical disorder caused by vaccinations, in particular the tetanus vaccination and/or antibiotics.

[2014 May] Rearranging the Deck Chairs on the Deck of the MHRA (UK FDA) By Martin Walker

[UK Jan 2007 B17] Vitamin seller made a criminal----MHRA worked with BBC Wales to entrap Jim Wright.

[2010 Nov] Drugs linked to brain damage 30 years ago  Secret documents reveal that government-funded experts were warned nearly 30 years ago that tranquillisers that were later prescribed to millions of people could cause brain damage. The Medical Research Council (MRC) agreed in 1982 that there should be large-scale studies to examine the long-term impact of benzodiazepines after research by a leading psychiatrist showed brain shrinkage in some patients similar to the effects of long-term alcohol abuse.  However, no such work was ever carried out into the effects of drugs such as Valium, Mogadon and Librium – and doctors went on prescribing them to patients for anxiety, stress, insomnia and muscle spasms.

[June 2007] MRC UK Refuses Autism/Bowel Disease Research

"The Medicines and Healthcare Products Regulation Agency found from information that had been in its possession for more than a decade that high doses of the anti-depressant can lead to aggression and thoughts of suicide. But instead of revealing the truth to the 17,000 people taking high doses and the other half-million Britons on a safer dose, the MHRA sat on its findings. Astonishingly, I was actually threatened with legal action by Professor Kent Woods, chief executive of the MHRA, if I revealed this."---RICHARD BROOK

On hearing of the MHRA for the first time, it might seem to many people that the MHRA is a 'normal' government regulatory agency. Few people would guess that the MHRA, while being the most important regulatory body for medicines in Great Britain, the organisation which, for example, processes Yellow Cards that notify the DH of averse reactions to drugs, is actually a trading company completely subsidised by the pharmaceutical industry. ....The history of the medicines regulatory agencies in Britain is a story of how the medical chicken crossed the road, from government participation and control of regulation to total immersion in the pharmaceutical industry.[Aug 2008] An Interest in Conflict? by Martin Walker MA

The Independent Review Panel for Advertising, primarily considers written representations from pharmaceutical companies as to the conformity of their advertising and promotional material with the Regulations, and to advise Health Ministers on the conformity of advertising and promotional material with the Regulations before a final decision is made by Health Ministers.   Both the IRPA and the IRPBP has a policy of members declaring personal and non-personal interests. The latest declaration of interests that can be found on the internet for both these committees are for 2004 and 2005.  It is frequent and common practice with both the MHRA and the DH, that they let site access to declared interests lapse over long periods....The IRPBP is an important committee within the MHRA.  The committee decides which treatments are considered medicines and which are not allowed to call themselves medicines. In terms of pharmaceutical industry competitiveness, this committee is very important. One of the issues in the fitness to practice hearing held for Dr Wakefield et al, involves the use and prescription of Transfer Factor. I do not know whether this product has at any time been discussed by the IRPBP. [Aug 2008] An Interest in Conflict? by Martin Walker MA

  The MHRA took over from the MCA in 2003. The MHRA is a Government Trading Fund; it might just as well be called a business or a corporation. A Trading Fund is an almost entirely separate economic entity which earns money by the provision of services and like any kind of company, it must balance the books at the end of each year. A trading fund is a government department, or an executive agency or part of the department, which has been established as such by means of a Trading Fund Order made under the Government Trading Funds Act 1973 (as amend the Government Trading Funds Act 1973, 26th July 1990). Typically, trading funds operate in very specialised fields and rely on their ability to derive income from their activities in order to cover their costs. Examples of trading funds are the COI and Ordnance Survey.
                   However, unlike a number of other Government Trading Funds, which provide services, earn money and accept fees from diverse ‘beyond government’ sources, the whole of the MHRA income is provided by one funder; the pharmaceutical industry. Further, a percentage of staff and executives of the agency, have come into it from the pharmaceutical industry.  It is therefore not surprising, that funded and partly staffed by the industry, its policies are shaped to please this sector.
                   The MHRA has the largest policing and enforcement department of any European medicines regulation agency, a part of the Enforcement & Intelligence Division (E&ID) of the Agency. Although contemporary government in Britain is characterised by quangos, and the attachment to Government of private vested interests, the MHRA is, as has been explained above, a business in itself which makes profit from the provision of services to the pharmaceutical industry. Inevitably there exists a high level of cynicism and some anger in the world of alternative medicine that, in effect, non-pharmaceutical treatments, which have not on the whole been proven harmful and against which no complaint has been levelled, are now regulated by a commercial concern which is managed, staffed and funded by the pharmaceutical industry. The cynicism is inevitably greater amongst those who realise that the pharmaceutical industry are also charged with overseeing the adverse reactions of their own medicines, which kill and maim many thousands of people.
                   From a legal point of view, perhaps the most worrying aspect of the MHRA, is that like the Atomic Energy Authority, it has its own police force, in this instance, paid for by the pharmaceutical industry. The two Divisions of the MHRA which are important in relation to the tracking of supplements and compliance and legal enforcement are firstly, the Medicines Borderline Section and the Enforcement and Intelligence Group, which gathers information on individuals who promote suspected medicines.
    The Group raid premises, make and take statements and confiscate products, computers and paper work. Although they are not police officers they can obtain warrants for raids from Magistrates and Judges. Enforcement often links up with Trading Standards Officers in local areas. ‘Officers’ in the enforcement group have their own powers conferred by the Medicines Act 1968 and subordinate legislation applying to the Act. These powers include the right to enter any premises to inspect, to take samples, to require production of any books or documents and to take copies of, or of any entry in, any such book or document. ‘Officers’ are bound by the Police and Criminal Evidence Act (PACE) and PACE codes of practice. It is a criminal offence to obstruct an enforcement officer. However, this particular police service stands well outside the discursive apparatus of accountability which exists either within the London Boroughs or at County level outside London. These enforcers are literally a law unto themselves – or more specifically, the law of the pharmaceutical companies.
                   When considering conflict of interests, the workings of the MHRA have to be seen in light of the fact that the agency is completely beholden to the multinational pharmaceutical industry.
[Aug 2008] An Interest in Conflict? by Martin Walker MA

The pharmaceutical industry has ferreted it's way into the medical-legal system in a way that no other industry could have managed. The regulatory body for the drugs industry, the MHRA (previously known by the massive euphemism as the Medicines Control Agency), which is meant to be a department of government within the Department of Health and answerable to the Minister for Health, is actually a trading organisation wholly funded by the pharmaceutical industry. In common with the Atomic Energy Authority and the British railway network, it has it's own police force, and is able to bring charges of the most serious nature against individuals; it takes people to court and the court can send them to prison. However none of the charges prepared and brought by the MHRA pass through the offices of the Crown Prosecution Service (CPS). None of the charges are overseen by any kind of independent body that measures the quality or even the quantity of the evidence. [21st July - 25 July] Tell me, how many forks are in your tongue? by Martin Walker MA

[Media 2000] Alarm as drug company chief joins watchdog    A top executive at one of the world's leading pharmaceutical companies is to become director of drugs licensing at the medicines control agency, raising questions about the independence of the MCA from the industry that it is supposed to police. Ian Hudson will take up his new job in February. He has worked in the drugs industry for the past 11 years and until recently was director and vice- president of Worldwide Clinical Safety, at SmithKline Beecham, and was to have led the worldwide drug safety group after the merger of SKB with Glaxo Wellcome, which came into effect yesterday.

It's virtually impossible to sue a pharmaceutical company in Britain, partly because of the difficulty of getting any funding for such actions. There's no point appealing to the government drugs watchdog—the MHRA. It is a small outfit entirely funded by the drug industry.  It has never taken any action against the academics who make fraudulent claims in ghostwritten articles, nor doctors working for the companies who repeat such claims, even when they have been shown to be untrue. So the only other body to turn to is the General Medical Council, whose job it is to investigate the conduct of doctors — but it has shown no inclination to act.  Why you should never trust new wonder drugs by Prof David Healy

"The Medicines and Healthcare Products Regulation Agency found from information that had been in its possession for more than a decade that high doses of the anti-depressant can lead to aggression and thoughts of suicide. But instead of revealing the truth to the 17,000 people taking high doses and the other half-million Britons on a safer dose, the MHRA sat on its findings. Astonishingly, I was actually threatened with legal action by Professor Kent Woods, chief executive of the MHRA, if I revealed this."---RICHARD BROOK

"The inquiry into the safety of the widely prescribed antidepressant drugs Seroxat and Prozac, and others of their class, has been halted by the medicines control agency after the revelation that two of its members have drug company shareholdings."--Media March 2003

"Its meetings are held in secret, and no minutes of proceedings, apart from revealing the names of attendees, are ever made public.  Any member who would dare step out of line and reveal proceedings to the press could face two years' imprisonment if the information compromised a drug company and its work.....It is one of the few drugs agencies in the world to be entirely funded by. . .the drugs industry."--WDDTY 2003

"The MCA is of course headed by a former top executive at SmithKline, Dr Ian Hudson."--Private Eye

"Professor Stephen Evans, of the Medicines Control Agency, said Dr Wakefield's paper was flawed and made a number of errors of fact. He said their trials had showed the MMR vaccine is as safe as the single measles vaccine."--Media

Professor Roderick MacSween, a professor of pathology at Glasgow Western Infirmary, had nearly £26,000 worth of shares in Glaxo ---SmithKline. [Media 3/2001] WATCHDOGS (MCA) LINKED TO MAKERS OF MMR JAB

Dr Michael Denham, a retired consultant in geriatric medicine and a member of the committee on Safety of Medicines External Advisory Panel, owned £250,000 worth of shares in GlaxoSmithKline. Professor Roderick MacSween, a professor of pathology at Glasgow Western Infirmary, had nearly £26,000 worth of shares in Glaxo ---SmithKline. [Media 3/2001] WATCHDOGS (MCA) LINKED TO MAKERS OF MMR JAB

Dr Michael Donaghy, a brain specialist at Oxford’s Radcliffe Infirmary Hospital, who sits on the MCA had £19,000 worth of shares. 11 professors and doctors have received fees for research from Aventis Pasteur. [Media 3/2001] WATCHDOGS (MCA) LINKED TO MAKERS OF MMR JAB

"A Sunday Express investigation has found that nearly a third of the 181 experts who sit on the Medicines Control Agency (MCA) committees are linked to GlaxoSmithKline, Aventis Pasteur or Merck, Sharpe and Dohme......The MCA has continued to endorse the triple measles, mumps and rubella (MMR) jab despite concerns linking it to autism and stomach disorders. But the extent of the MCA members’ financial ties to MMR manufacturers raises questions about potential conflicts of interest."--Sunday Express

"Two important new scientific studies 1,2 do not support the suggestions that MMR or MR vaccines may cause autism or Crohn's disease. These studies represent objective scientific work undertaken into theories about the safety of MMR or MR vaccine. Both studies support the conclusions of earlier safety reviews carried out in 1997/1998 by independent expert committees; the Committee on Safety of Medicines (CSM) and the Joint Committee on Vaccination and Immunisation, and the Medical Research Council.   1. Committee on Safety of Medicines, Report of the Working Party on MMR vaccine; May 1999. 2. Taylor, B. et al. Autism and measles, mumps and rubella vaccine: No epidemiological evidence for a causal association. Lancet in press; June 1999."

It was impossible to prove or refute the suggested associations between MMR vaccine and autism or inflammatory bowel disease because of the nature of the information, the self-selection of cases and the lack of comparators. Nevertheless, the Working Party found that the information available did not support the suggested causal associations or give cause for concern about the safety of MMR or MR vaccines.