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One thing that has come out of the COVID response is how it’s exposed the pharmaceutical industry to more scrutiny from the public than ever before. More questions have been raised about the Therapeutic Goods Authority (TGA) and our Health Pharmacrats than ever before. Yet, what is the alternative?

In this parliamentary speech, I put it on record that we must look at the influence of pharmaceutical companies on the education system for medical professionals, and the relationships between pharma giants and former health department executives. The toxic, inhuman killer ‘pharmaceutical only’ model is failing Australian taxpayers. People are dying needlessly.

As an example, Albicidin is a natural antibiotic with clear potential to become our leading antimicrobial. It’s proven to not create resistance. Albicidin could be, and most likely is the answer to antimicrobial resistance. There are many others, but they don’t get patented. They don’t receive sponsorship and therefore they don’t get approved.

It’s time for an entirely new medical paradigm. One that puts humans first, not big pharma.

Antimicrobial resistance is the new climate change, allowing for control over agriculture, medicine and household and industrial cleaning, in the name of reducing use of antimicrobials. That’s why an alternative solution, using an antimicrobial that doesn’t cause antimicrobial resistance, is being ignored and quietly buried. It’s to protect globalist profits and to control people – and to hell with human and animal health and safety!

Globalists WANT control. Globalists NEED control to complete their agenda.

Australia needs a customer consumer advocate, or natural product advocate, to advance natural products that can’t be patented, yet are safe and effective treatments — products to be listed under Schedule 4 and offered under the PBS as frontline medicines. Not watered down products sold in supermarkets as complementary medicines so that their efficacy can plausibly be dismissed.

Instead of advancing people-first health care, our Pharmacrats are actively promoting mRNA vaccines and medications to the commercial benefit of big pharma. This is caused by “the patent cliff”, which refers to the expiration of patents on popular drugs, leading pharmaceutical companies to face intense competition from generic drug makers, dramatically reducing their profits. The new mRNA technology allows big pharma to replace off-patent drugs with newly patented mRNA drugs at prices that guarantee their profits for the next 30 years. Our health authorities are actively promoting this solution to the patent cliff, despite the myriad of adverse health outcomes from the mRNA vaccines.

Why? These are important matters that can only be answered by a Royal Commission.

What should not wait for a Royal Commission is a system to incorporate affordable, natural remedies into our health approval process. This could be implemented immediately if the Pharmacrats were interested in providing people-first health care.

Transcript

Where’s the scrutiny on our health authorities? During COVID, drugs were rushed through that would never have been approved on safety and efficacy grounds, such as molnupiravir and remdesivir. Last year, these two inhuman pharmaceuticals cost taxpayers $1 billion. Alternatively, tried and tested drugs that are out of patent could have been used for a fraction of the price. Remember that our authorities and the mouthpiece media called ivermectin ‘horse paste’. The statist Left rushed to demonise anyone who defended ivermectin, because the control side of politics—the so-called Left—loves to follow orders. Ivermectin is a Nobel-Prize-winning antiviral for humans. Over 40 years, it has saved millions of lives. Around the world, it’s now been proven safe and effective as an early-stage treatment for COVID, as it always was.

Our health authorities demonised ivermectin to prevent early-stage treatment of COVID in order to build demand for an untested novel mRNA vaccine. How many died because of the long-term strategy that our health authorities followed and pushed—a strategy to use COVID as a cover to introduce a class of mRNA drugs that the public would have rightly baulked at and rejected? How many died from the side effects of mRNA technology—technology that was not tested in Australia and was not tested off the production line, for which the method of production was changed after overseas testing and approval and the fake trials were at best shambolic and at worst criminally negligent?

Why would our health authorities tolerate this? Simply because of a thing called the patent cliff. Pharmaceutical companies are profitable because they develop a new drug and then get a patent, exclusive sale of the drug for 25 years. Drug companies can afford to put that drug through the approval process because once it’s approved they add the approval cost to the selling price—kerching, kerching!

The system of drug patents has created a $2 trillion industry whose tentacles of influence extend to political parties, who happily accept donations, and to health authorities. Their tentacles extend to the USFDA and Anthony Fauci’s National Institutes of Health, who hold patents on drug processes they license to big pharma in return for hundreds of millions of dollars in personal royalties. Their tentacles extend to the World Health Organization, the United Nations and the World Economic Forum, whose young global leaders sit in this parliament.

This is influence that our healthy authorities cultivate while coveting lucrative careers in the pharmaceutical industry. For example, just eight months after approving Pfizer’s untested COVID injections, Professor John Skerritt, former head of the Therapeutic Goods Administration, the TGA, is now on the board of the pharmaceutical industry lobby group Medicines Australia. This isn’t the normal operation of a free-enterprise system that One Nation would support; this is a cabal of greedy, unprincipled, evil individuals treating everyday citizens as cash cows. They want everything you have for themselves, including your health.

The patent cliff is upon us. There’s increasing urgency—desperation—in the measures being rammed through government. Two-thirds of the revenue is from drugs being sold to you that are out of patent now or will go out of patent over the next five years. That threatens big pharma’s harvesting of humans for profit. Modern drugs, once out of patent, can be made for cents per tablet. India specialises in that. Australia used to, and we can do it again. The patent cliff threatens the entire pharmaceutical industry and stops the ability of chemical pharmaceuticals to do better than they do now, in terms of profit.

From where are the new patents going to come? I’m glad you asked, Mr Acting Deputy President: from mRNA of course. There are 400 new mRNA vaccines and drugs currently under development. Such is the expected volume of these things that two manufacturing plants are being prepared here in Australia. Our health authorities decided to press ahead with mRNA technology to save the pharmaceutical status quo—the pharmaceutical gouging of people to extract exorbitant profits. Patient harm apparently no longer matters.

Last week, a study of 99 million COVID-jab users, including in New South Wales and Victoria, found the product was not safe. The study was published by Elsevier, for more than 140 years the world’s leading scientific publisher and data analytics company. The study showed the following conditions were occurring above baseline levels: brain and spinal cord swelling, up 380 per cent; blood clots, up 320 per cent; Guillain-Barre syndrome, up 250 per cent; and myocarditis, up 278 per cent for Moderna and up 350 per cent for Pfizer. After a second injection, myocarditis was up a damning 610 per cent and pericarditis was up 690 per cent. I told you so four years ago. Many good people warned that COVID products were not tested, that they were experimental, and that forcing them on the general population was an insane, inhuman abuse of government power. Now look at those figures. It’s another area for a royal commission to investigate.

It’s time for an entirely new medical paradigm in this country and throughout the West. Pharmaceutical companies are embracing mRNA as their saviour because it can be patented. They can charge whatever they want for it, and compliant health bureaucrats like our TGA, acting out of self-interest, protect pharmaceutical companies from financial harm. The expert medical advice the TGA relies on comes either directly from drug companies or from advisers who have worked for big pharma, who have accepted research grants or sponsorship from big pharma, or who covet doing so in the future. After all, $29-million Sydney harbourside mansions don’t just buy themselves.

These are things that make for a royal commission. One thing that should not wait for a royal commission is a system for getting cheap, natural remedies into our health approval system. Australia needs an office of the consumer advocate to oversee complaints and the harm bureaucrats cause—bureaucrats who appear incapable of acknowledging odious and obvious adverse events. We need a customer consumer advocate or a natural product advocate to advance natural products that can’t be patented but are safe and effective treatments—products to be listed under schedule 4 and offered under the PBS as frontline medicines, not watered down and sold in supermarkets as complementary medicines so their efficacy can be dismissed. Albicidin, for example, is a natural antibiotic with clear potential to become our leading antimicrobial. It’s proven to not create resistance. Albicidin could be the answer, and highly likely is the answer to antimicrobial resistance.

Antimicrobial resistance is the new climate change, allowing for control over agricultural, medicine, and household and industrial cleaning in the name of reducing use of antimicrobials. That’s why an alternative solution, using an antimicrobial that doesn’t cause antimicrobial resistance, is being ignored and quietly buried: to protect globalist profits and to control people—and to hell with human and animal health and safety! Globalists want control. Globalists need control to complete their agenda.

Take another example: blushwood is an Australian native berry. It was shown, in a 2014 test, to kill skin cancer in just 10 days. Did our health authorities rush to understand this plant and bring a potentially lifesaving medication to market? No; they did not. Another one: conolidine is a natural treatment for severe pain. Ignored! Natural remedies include cannabis. Senator Pauline Hanson has led way, advocating for medicinal cannabis since 1996. I joined her, and now there are others.

A recent paper pointed out that natural products work differently to chemical products, yet our system for understanding and testing substance efficacy is geared to chemical drugs. The paper and system offer a new way of measuring efficacy that confirms plants like cannabis and conolidine do work, and explains how they work. The truth is this: currently only when a product is patented and presented as the TGA on a plate, ready for the TGA’s rubberstamp, does it enter our pharmaceutical system. I urge the Minister for Health and Aged Care to introduce a consumer natural products advocate to provide much needed supervision and accountability over our health authorities. Failing that, I ask the Greens to consider if the agency they’re establishing with the Legalising Cannabis Bill would be better suited to handle natural medications in general—those that the TGA refuse to handle in addition to cannabis.

I’m not offering medical advice on the examples I’ve used in this speech; I’m asking why the health department and medical schools first response is to the scalpel and the prescription pad instead of natural medications that cost a fraction of the price. We must have an independent office in the TGA with the budget to sponsor natural alternatives through the safety, testing and efficacy stages, and to have these promoted to doctors who most likely have never even heard of them.

We must look at the influence of pharmaceutical companies in the education system for medical people, in their relationship with former health department executives and their influence through advertising and sponsorship. The toxic inhuman killer ‘pharmaceutical only’ model is failing Australian taxpayers. People are dying needlessly. Stop so-called health authorities committing homicide, child homicide, infanticide. As a servant to the people of Queensland and Australia, I say call a royal commission now and make an immediate start on the obvious reforms to our health administration that we need.

Many Australians have lost trust in governments at both state and federal levels, and we’ve lost trust in health authorities. Last parliament the Select Committee on COVID-19 stated ‘a royal commission be established to examine Australia’s response to the COVID-19’. That was two years ago. During his election campaign, Prime Minister Anthony Albanese promised the Australian people a COVID Royal Commission. He and Minister Gallagher, who chaired the committee, have both broken their promises.

The Government has clearly chosen to cover-up for the failure of our health authorities to apply human rights to our COVID measures. A genuine party of the worker would be protecting workers against the billionaires who profited from COVID.

The Albanese government must restore trust and commit to a royal commission now. The royal commission could easily commence as soon as the current Senate’s inquiry into appropriate terms of reference defines those terms — an inquiry One Nation secured. I promised to hound those responsible down and I will keep that promise.

Transcript

Today the Queensland Supreme Court ruled vaccine mandates for Queensland’s emergency services workers to be unlawful. What a victory for the Australian people! It’s a victory that reaffirms the need for a full royal commission into Australia’s response to COVID. Everyday Australians have lost trust in governments at both state and federal levels, and we’ve lost trust in health authorities. Recommendation 17 of the report of the Select Committee on COVID-19 stated ‘a royal commission be established to examine Australia’s response to the COVID-19’. That was two years ago.

During his election campaign Prime Minister Anthony Albanese promised the Australian people to hold a COVID royal commission. He and Minister Gallagher, who chaired the committee, have both broken their promises. Appearing to have something to hide looks terrible for the government. It is terrible for the government. The public realise that our Prime Minister and his administration cannot be trusted to keep their word.

Today’s Queensland Supreme Court ruling is encouraging for everyday Australians who’ve lost their source of income. Businesses were forced to lay off their staff unless they complied with the draconian policies, and many industries are still suffering the consequences of having to fire unvaccinated staff. Our nurses, teachers, police, firefighters and paramedics, along with other Australians, deserve to know where things went wrong and why the government turned against them. One simple green tick was the difference in being able to attend school, go to work, move around, socialise and exercise—one green tick that took our rights to freedom, life, privacy and movement.

The Prime Minister must now realise that, if he takes these things from the people, trust goes with them. The Albanese government must restore trust and commit to a royal commission now, to commence as soon as the current inquiry into appropriate terms of reference defines those terms.

The Queensland Supreme Court said there was an abuse of process and that they did not consider the loss of human rights fundamental to Australian democracy. 

Remember when Ivermectin was called a horse paste and they said humans shouldn’t even take it?

Now the World Health Organisation is handing it out to a million humans. 🤷

I was disappointed in the Minister’s response to my questions about the implications of the QLD Supreme Court judgement on the COVID ‘vaccine’ mandates. I expected more clarity and less deflection from the Minister. These decisions were made by the Liberal, Labor and Greens parties, there can be no avoiding the fallout form their actions across the COVID period.

While the ruling was made on the basis of the human rights act in QLD, identical provisions are in place in Victoria and the ACT, suggesting the decision is not just a QLD issue. The government is arrogantly ignoring the reality of the situation and failing to read the room when it comes to this topic.

People have had enough of high-handed, out of touch government. One Nation is calling for the Royal Commission into our COVID response to be announced right now!

Transcript

I take note of Senator Gallagher’s answer to my question on the Queensland Supreme Court’s decision. The court found measures relating to COVID were mandated on a number of Queensland workers without adequate consideration of their human rights as required under the Queensland Human Rights Act. Identical human rights provisions apply in Victoria and the ACT. So certainly there is the probability of the same or similar decisions being made in other jurisdictions.  

I’d hoped the government would be fully aware of the implications of this decision. I was disappointed. The minister deflected and failed to address the substance of the question, so here are some more reasons the minister should get clarity on this issue. An employee who is fired as the outcome from a vaccine mandate can sue the employer, which may be the government, for wrongful dismissal. An employee who took a vaccine to keep their job as a result of a vaccine mandate, who is now vaccine injured, can sue for damages. Class-action lawsuits will result from this decision. The Commonwealth will be as much in the firing line as Victoria and Queensland.  

It’s not just mandates. Evidence has been presented over the last few months that closing schools and denying children education has caused a permanent drop in children’s educational potential and medical health—permanent harm. Last week, a landmark study of 99 million people including Australians found the injections caused an increase in blood clots, brain injuries and heart disease of up to 600 per cent. These injuries are legally actionable. Whether it’s over mandates, vaccine injuries, education or business closures, victims will be joining class-action lawsuits sooner rather than later.  

All levels of government in Australia made terrible mistakes during COVID. Only a royal commission has the powers and the resources to decide what mistakes were made and how the victims of those mistakes can be fairly compensated. This will be expensive, yet failure to act through a royal commission will create a running sore on public administration for a generation. Only an objective royal commission will restore trust in governments and in the healthcare sector. 

In January, the Senate held a committee inquiry into appropriate Terms of Reference for a Royal Commission into COVID. This is the Royal Commission the Prime Minister promised during the election campaign, which Senator Gallagher also promised. Instead the Prime Minister called a review of the government’s response, which excludes state and territory responses.

Many have slammed the Prime Minister’s COVID review panel as a “toothless tiger” and support a Royal Commission instead. Doctors, unions, human rights lawyers, vaccine injured, and Royal Commission experts were among the witnesses who provided submissions and gave evidence at the Senate inquiry tasked with proposing Terms of Reference for a future COVID Royal Commission.

Why did the Government Health Department not partake in this inquiry? Could it be to avoid scrutiny from the Committee that would result from making a submission? Judge for yourself.

Transcript

Senator ROBERTS: The department and its agencies did not make a submission to the Senate inquiry into appropriate terms of reference for a possible future royal commission into COVID. I would have thought, Minister, that the department that ran our COVID response would be the first to put forward its position on the matter. Why the silence? Is the department hiding from committee scrutiny? 

Senator McCarthy: We do have an inquiry underway—an independent one—looking into COVID, so I reject outright your question. 

Robodebt had a Royal Commission called three months after Anthony Albanese was elected.

Four years after we first heard of COVID and two years after Albanese was elected, we still don’t have a COVID Royal Commission.

Is PM Albanese only interested in “transparency and accountability” when it’s politically convenient for him?

The Senate inquiry to draft terms of reference for a future COVID Royal Commission is having its first public hearing today (Thursday, 1 February 2024) in Canberra.

This committee will report on what the appropriate terms of reference will be to give all Australians a say and have a fully empowered Royal Commission into the COVID mismanagement.

Panel at Inquiry

  • Institute of Public Affairs (Submission No. 14)
  • Australian Institute for Progress (Submission No. 39)
  • Redfern Legal Centre (Submission No. 9)
  • Australian Human Rights Commission (Submission No. 18)
  • Civil Liberties Australia (Submission No. 13)
  • People’s Terms of Reference (Submission No. 45)
  • Nurses Professional Association of Queensland (Submission No. 46)
  • Australian Nursing and Midwifery Federation (Federal Office) (Submission No. 46)
  • The Royal Australian College of General Practitioners Ltd (Submission No. 41)
  • Suicide Prevention Australia (Submission 21)
  • COVERSE (Submission 34)

Founded in 1963, the NSW Council for Civil Liberties (NSWCCL) charter “is to protect the rights and liberties of Australian citizens and to oppose the abusive or excessive exercise of power by the state against its people.”

In their submission to the COVID Royal Commission terms of reference inquiry, NSWCCL says “we are an organisation that champions the rights of all to express their views and beliefs without suppression.” They then continue in their one page submission to say:

1. an inquiry should cover “the extent to which public health interests were adversely affected by misinformation about COVID disseminated by Senator Roberts and people associated or aligned with his views.” (I guess they mean about adverse reactions to the jab, the Wuhan lab leak theory, ineffective masks and the made-up 6 foot social distancing rule, all true?)

2. There should be an “inquiry into appropriate means for protecting the public from misleading information”

3. The government’s proposed Misinformation and Disinformation Bill doesn’t go far enough.

4. “it is not appropriate for a Royal Commission to be held in respect of the COVID-19 pandemic”

How can an organisation that calls itself a champion of civil liberties and fights for free expression argue:

1. an entire section of the community should be silenced

2. the government should have unprecedented power to shut people down

3. Australians should not be able to have a say at a Royal Commission into the largest invasion of civil liberties in modern history?

With the origin of COVID now known to be the result of gain-of-function research, funded by the United States through Anthony Fauci’s NIH and conducted in Wuhan China to escape regulatory barriers, it’s even more important that Australians have input into the Terms of Reference for a COVID Royal Commission.

If any member of the public, medical profession, whistle-blower or other interested party wishes to make a submission I urge them to have their say to the committee via this link:

https://www.aph.gov.au/Parliamentary_Business/Committees/Senate/Legal_and_Constitutional_Affairs/COVID19RC47

With Moderna setting up mRNA vaccine production in Australia, it is concerning that both the Morrison and Albanese governments have provided 16 vaccine indemnities since the COVID outbreak. That means the bill to compensate those who are harmed by these products falls on taxpayers, not the pharmaceutical industry that rolled out their products with indecent speed.

There are 400 new mRNA vaccines under development to replace the off-patent conventional vaccines. Responsibility for harm from these products must rest with the makers, not the public.

The emerging pattern of adverse events and deaths correlating with the COVID injections is overwhelming. It must be objectively examined and not simply dismissed. There is no reason why these COVID injections should not be given proper scrutiny in the same way we scrutinize health effects from lockdowns, economic hardship, inadequate healthcare provision or even inappropriate treatments for the virus. Is there? What is in the Pfizer contracts that we should know about?

Transcript

As a servant to the many and varied people who make up our one Queensland community, I would like to update my constituents on the committee inquiry One Nation secured looking into terms of reference for a royal commission into SARS COVID-19. The committee has set 12 January 2024 as the deadline for submissions. If any member of the public, medical profession, commercial entity or interested party wishes to, they can make a submission. It can be confidential if you want. I’ll post a link on my social media and on my website, and I urge whistleblowers, senior medical practitioners and academics to have their say. I’ve received many suggestions for terms of reference and, firstly, can I say: please tell the committee. That’s the process. 

Let me talk about the terms of reference. Firstly, the origin of COVID. An article in today’s Australian by Sharri Markson sets out proof—and I do mean proof—that COVID was engineered as a result of gain-of-function research funded through America’s National Institutes of Health and its former director Anthony Fauci. The research was conducted in China because it was out of reach of America’s regulations, and it was cheaper. Gain-of-function research is supposedly so that health authorities can create new viruses and then an antidote or a vaccine so that if nature supposedly produces that virus, there will be a vaccine ready to go. 

Secondly, vaccine indemnity. I spoke this week about a little-known fact: Australia has provided 16 vaccine indemnities in recent years. Now, an indemnity doesn’t prevent a person who has been harmed from suing, it just means any damages are paid with taxpayer money and not big pharma money. Pharmaceutical companies keep the profits and taxpayers pay for the damages. Even more troubling, the Albanese Labor government has provided Moderna with a blanket immunity for every vaccine they make in the new Australian factory. There are 400 mRNA vaccines under development. Not all will be made in this plant, yet many will be. The Morrison and Albanese governments are normalising vaccine indemnity. I want to know why. The terms of our contract with Pfizer must be examined, as we were still signing hidden purchase contracts as recently as last month. 

Surely this pattern of adverse events and deaths tracking injections upward and downward proves causation of vaccine deaths by their tens of thousands. The science is now overwhelming. This can’t be ignored and must be investigated. (Time expired) 

In light of Professor Brendan Murphy’s, the Secretary Department of Health & Aged Care, evidence during the June estimates that mandates are no longer justifiable, I asked the Human Rights Commissioner, Lorraine Finlay, for their latest guidance on COVID vaccine mandates.

Commissioner Finlay’s response was that this advice has not changed throughout the COVID response in terms of general human rights principles. What this means is that although governments can restrict individual human rights in an emergency, those restrictions need to be proportionate, non-discriminatory and targeted to risk.

This goes to the heart of the problem. Decisions were made that put Australia onto an emergency footing in 2020. Yet this has dragged on beyond what is reasonable. The response has not been proportionate to the risk of the COVID infection, which the Chief Medical Officer in March of 2021 admitted was low to moderate.

Discrimination remains to this day against those who exercised their right to say no to injections, despite the coercion. We must have a system in place whereby civil liberties are rightfully returned. The Australian Human Rights Commission should be at the forefront of calling for this, yet they appear to be captured, with the exception of Commissioner Finlay, who has come out strongly in support of human rights principles.

Commissioner Finlay is looking forward to the COVID Inquiry that was recently announced, after the Senate approved my motion to establish an inquiry to recommend and report on the Terms of Reference for a COVID-19 Royal Commission. She sees the need not only to look at the economic and scientific impacts and advice that were given throughout the COVID response, but the human cost too.

Transcript

CHAIR: Senator Roberts, do you want to see if you can get some questions done?

Senator ROBERTS: Yes. As the chair said, my questions are fairly short and straight to the point. What is the latest guidance from the commission on COVID vaccine mandates? Where was that published?

Ms Finlay: I would refer you to the answer we gave you in relation to this at the previous estimates. The advice remains the same in terms of the general human rights principles that we rely on in our approach to both
vaccine mandates and all other restrictions that were imposed during the COVID-19 pandemic.

Senator ROBERTS: I must compliment you here and express my appreciation and admiration for your stand on being so clear on the Voice and on misinformation and disinformation. I also want to thank everyone for being here tonight so I could do that. Are you aware of the evidence from the Secretary of the Department of Health and Aged Care, Professor Brendan Murphy, at the previous estimates in regard to COVID mandates?

Ms Finlay: In a general sense.

Senator ROBERTS: On 1 June, Professor Brendan Murphy said – at this stage in the pandemic there is little justification for vaccine mandates. That is the most senior health bureaucrat in the country who said that. There doesn’t seem to be any updated guidance from the commission on vaccine mandates despite the fact they are still in effect at employers and are clearly a breach of human rights that’s not proportionate to any supposed benefit. Why haven’t you come out clearly on this issue?

Ms Finlay: I would answer that in two respects. The first is that the guidance in terms of the general human rights principles remains the same. We are not medical experts. I think we discussed that at the previous estimates. Our advice is based on those general human rights principles where in emergency situations governments can restrict human rights but those restrictions need to be proportionate, nondiscriminatory and targeted to risk. So the advice remains the same because of the general principles of international human rights law that we rely on in informing our views about these things and those don’t change.

Senator ROBERTS: So you as a commission essentially follow blindly? The Chief Medical Officer advised me in March 2021 that the severity of COVID was low to moderate, not severe. So it was not a crisis.

Ms Finlay: No, our advice doesn’t follow blindly. Again, I would refer back to the evidence we gave previously and note that, for example, the most recent TGA advice in relation to their vaccination safety report
repeated the same advice that we discussed at the previous estimates in terms of the benefits of the vaccination outweighing the risks. It’s on the basis of that that the general principles of human rights law then apply.

Senator ROBERTS: I appreciate that you probably haven’t got any latitude to investigate, but the TGA told me at Senate estimates in February, I think, that they did not test the injections. They relied on the FDA in
America, which did not test injections. It relied on Pfizer, which shut down the trial because of the horrendous results.

Ms Finlay: I can’t provide any information on that—

Senator ROBERTS: No, I wasn’t expecting that. I’m just—

Ms Finlay: but I would refer to the second aspect of the answer that I was meaning to get to, which is that we welcome the opportunity for these issues to be explored at the COVID-19 inquiry that’s been announced. Certainly we have made public comments in relation to that inquiry about the need to not only look at the economic and scientific impacts of advice that was given throughout the pandemic but at the human cost of the
pandemic as well.

Senator ROBERTS: That’s refreshing to hear. Thank you.