Thank you Malcolm, you are a man of honesty, courage and determination.
Gavin says:
I really would have hoped that before plunging a country into debt with lockups and forcing untested “vaccines” on the citizens, they would have had the care to just check the data. Is it too much to ask? It is not as if the origins of the problem and solutions at the ready are not extremely suspicious to begin with. Even more shocking is when confronted with peer-reviewed disagreement on something which for decades would have been a clear experiment, the scientists lose to a mere fobbing off by the people who should be putting mere doubt above testing further.
Damien Murray says:
Hi Malcolm,
I appreciate your questions – very important, very relevant. I’m seriously unimpressed with the responses received – no data, just generalised assertions about their processes and clearly no intent to investigate or counter your statements. I don’t know about the personalities that you question in Senate estimates, but im particularly unimpressed by her performance. Its obfuscation, playing politics, disgusting and inappropriate game playing. People are suffering as a result of the TGA’s negligence in following up safety data before the roll out and adverse events, damning research papers and the testimony of concerned medicos after the rollout out. The hubris and sheer lack of concern is both frightening and inhuman. Thankyou Senator Roberts for your unceasing efforts to try to bring some accountability to our political processes and agencies.
Sincerely Damien Murray
Simon says:
The TGA would have know that there was no legitimate clinical trial performed by any of Big Pharma. Emergency use Authorization (EUA) Countermeasures in the US do not require clinical investigations.( ie no valid trials). This has already occurred for over 100 other pharmecutical drugs in the last decade. It was the US DoD Department of Defence that requested the so called vaccinations be produced in the first place. When Pfizer was challenged in court for the release of clinical trial documents (withheld for 75 years) it was attorneys from the (DOJ) Department of Justice that represented Pfizer not attorneys from Pfizer. I wonder why ?
Brooke Jackson has since taken Pfizer to court in the US for fraud. Pfizers attorneys turned up for this one and they have asked the judge to dismiss the case and filed the following motion. ‘We (Pfizer) did not defraud the government we delivered the fraud that the government ordered’ Von Sasha Latpova investigated this in January 2023 and has documentary proof. Why would the TGA read any clinical trials that they would have known were Demo (not valid).
Thank you Malcolm, you are a man of honesty, courage and determination.
I really would have hoped that before plunging a country into debt with lockups and forcing untested “vaccines” on the citizens, they would have had the care to just check the data. Is it too much to ask? It is not as if the origins of the problem and solutions at the ready are not extremely suspicious to begin with. Even more shocking is when confronted with peer-reviewed disagreement on something which for decades would have been a clear experiment, the scientists lose to a mere fobbing off by the people who should be putting mere doubt above testing further.
Hi Malcolm,
I appreciate your questions – very important, very relevant. I’m seriously unimpressed with the responses received – no data, just generalised assertions about their processes and clearly no intent to investigate or counter your statements. I don’t know about the personalities that you question in Senate estimates, but im particularly unimpressed by her performance. Its obfuscation, playing politics, disgusting and inappropriate game playing. People are suffering as a result of the TGA’s negligence in following up safety data before the roll out and adverse events, damning research papers and the testimony of concerned medicos after the rollout out. The hubris and sheer lack of concern is both frightening and inhuman. Thankyou Senator Roberts for your unceasing efforts to try to bring some accountability to our political processes and agencies.
Sincerely Damien Murray
The TGA would have know that there was no legitimate clinical trial performed by any of Big Pharma. Emergency use Authorization (EUA) Countermeasures in the US do not require clinical investigations.( ie no valid trials). This has already occurred for over 100 other pharmecutical drugs in the last decade. It was the US DoD Department of Defence that requested the so called vaccinations be produced in the first place. When Pfizer was challenged in court for the release of clinical trial documents (withheld for 75 years) it was attorneys from the (DOJ) Department of Justice that represented Pfizer not attorneys from Pfizer. I wonder why ?
Brooke Jackson has since taken Pfizer to court in the US for fraud. Pfizers attorneys turned up for this one and they have asked the judge to dismiss the case and filed the following motion. ‘We (Pfizer) did not defraud the government we delivered the fraud that the government ordered’ Von Sasha Latpova investigated this in January 2023 and has documentary proof. Why would the TGA read any clinical trials that they would have known were Demo (not valid).