Steps NIH, CDC, NIAID, and FDA must take day one on swearing in of all new Directors & Robert Kennedy Jr. as HHS Secretary must ensure that heads as appointed must meet these goals; this is baseline

I do have super confidence in RFK Jr. in stopping the corrupted conflicted reach that BIG pharma has into the alphabet health agencies; these represent immediate goals & please add in comments

I strongly support Robert Kennedy Jr. moving forward.

Repost.

The health and research alphabet agencies under HHS (including points below applicable to HHS) MUST focus on the following immediately on the nominated heads e.g. FDA Commissioner, CDC Director, NIH Director etc. being approved. The turnaround time for action must be at most 6 months from approval e.g. July 15th 2025.

All of the following points addressed to FDA, NIH, NIAID, and CDC (call to action) apply to HHS under Robert Kennedy Jr. in the case of actions it the HHS must also take:

NIH

1)NIH (National Institutes of Health): must initiate and implement research studies and programs that examine the Malone Bourla Bancel Weissman et al. mRNA technology vaccine injures that have accumulated

NIH must join and partake with CDC etc. acute surveillance of Malone Bourla Bancel Weissman Sahin et al. mRNA technology vaccine harms and deaths across time

NIH must revisit all the COVID Operation Warp Speed (OWS) related studies (it funded) it funded and convene an expert panel to examine the research protocols, the methods, the statistics used, the findings, and the funding approved. Findings are to be made known to the public in 6 months of the new NIH Director taking lead.

There is no existing randomized placebo-controlled study double blinded, or triple blinded that shows that the COVID mRNA gene vaccines reduced hospitalization, death, ICU, severe illness etc. in children or adults, elderly etc. The NIH Director must reveal to the public what studies the NIH (past and existing under new leadership) uses to support that statement that the mRNA vaccine reduced hospitalization and death and was beneficial to the public, e.g. in the elderly.

NIH must also initiate a review of all ethics review panels and input that was used to authorize the COVID related studies and findings made known to the public in 6 months of the new NIH Director taking lead.

NIH must immediately stop all gain-of-function (GoF) or related research in any US affiliated or funded or operated biolab anywhere in the world. NIH must stop its involvement (direct or indirectly) all bioweapons biological research in US laboratories and anywhere globally that the US is affiliated to. No US tax-payer money must be used for any such research anywhere in the world.

The NIH Director must IMMEDIATELY call for the end of any mRNA technology gene-based vaccine research.

The NIH Director must call (with the new FDA Commissioner) for the Malone et al. mRNA gene vaccine to be removed from market, complete, and immediately on swearing in. None to be made available to infants, children, teens, adults, elderly. No moratorium.

The NIH Director must ensure that any studies for mRNA vaccines touted under ‘new and improved’ ‘minor adjustments’ etc. must run for at least 20 years of proper duration, sample size, patient-important outcomes, gold-standard trustworthy research methods, and with all the necessary safety follow-up. Any such study must have proper ethical debate and accompanied by cost-effectiveness analyses. Drugs and vaccines and medical devices must not only meet safety and effectiveness threshold but there must be a dedicated examination of if the drug or vaccine is NEEDED, necessary.

NIH must return to the 1972/1975 Nixon era and agreements (1969 to 1976 Nixon era, the Biological Weapons Convention (BWC), or Biological and Toxin Weapons Convention (BTWC) 1975 relating to weapons of mass destruction) and renounce the use of lethal biological agents and weapons, and all other methods of biological warfare. Renounce its role in such lethal biological agents and weapons. NIH will confine its biological research to defensive measures such as immunization and safety measures and work with the Department of Defense in disposing of existing stocks of bacteriological or any such weapons or specimens. The same posture for NIH in use or research in and of lethal chemical weapons.

NIH must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies.

NIH is to take no funding or donations from any pharmaceutical industry parties etc.

NIH must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.

NIH Director must examine each unit, department, entity under its purview and if a duplication or a waste of tax-payer money, if not a functional high-quality entity within NIH, then it must be shut down. Top level technocrats must be removed, reassigned and if possible, cut 25% of all staff across the board. This examination must begin on the first day of being sworn in as the new head.

FDA

2)The Food and Drug Administration (FDA) must disband the current drug and vaccine research and related EUA and BLA panels, decision groups, advisory boards, external and internal boards and make know to the public all the decisions and what went into them across COVID for all COVID decisions.

The FDA commissioner must IMMEDIATELY call for the withdrawal of any and all mRNA technology related vaccines e.g. Pfizer, Moderna etc.; complete; this must include a complete removal from market with witnessed destruction of any supplies.

The FDA commissioner must IMMEDIATELY call for the end of any mRNA technology gene-based vaccine research. Complete.

FDA Commissioner (incoming) must commit to end the revolving door between itself (Commissioners) and BIG Pharma, that he himself/herself will accept no position within BIG Pharma for at least 5 years post leaving the FDA post.

The FDA commissioner must state immediately that there will not be any FAST TRACK approvals of any future products especially vaccines that come to it for approval.

The FDA commissioner must initiate a public open examination of all EUAs granted to Pfizer and Moderna etc. as it relates to all COVID mRNA vaccines, DNA viral vector, any drugs e.g. Paxlovid etc. In fact, any and all medications and vaccines and any sort of ‘countermeasure’ that the FDA gave EUA approval for up to this date.

The FDA must initiate new and proper vaccine and drug advisory boards within 2 weeks of the new FDA lead taking over.

The FDA must make available to the public (in at most 6 months after approval of the incoming Commissioner) all the data, evidence, submissions, everything, that all organizations and entities submitted to it across COVID up to present, including all data and submissions that went into the FDA’s approval (EUAs) of the Pfizer and Moderna mRNA gene vaccines. All.

The FDA must call for an urgent meeting of all the vaccine companies e.g. CEOs Bourla, Bancel, Sahin etc. and all mRNA technology inventors e.g. Malone, Weissman, Tureci, Kariko etc. and especially those vaccine makers that manufactured Malone et al. mRNA gene vaccines e.g. Pfizer, Moderna, BioNTech etc. and in live open door public meetings, display all the harms, adverse event, death data it has (they have in possession) and allow all relevant external experts to attend to produce all the harms, adverse event, and death data that has accumulated since the roll-out of the mRNA vaccine. All aspects of the mRNA vaccine must be reviewed in public and all made available to the public within 6 months of the new FDA Commissioner taking office.

There is no existing randomized placebo-controlled study double blinded, or triple blinded that shows that the COVID mRNA gene vaccines reduced hospitalization, death, ICU, severe illness etc. in children or adults, elderly etc. The FDA Commissioner must reveal to the public what studies the FDA (past and existing under new leadership) uses to support that statement that the mRNA vaccine reduced hospitalization and death and was beneficial to the public, e.g. in the elderly.

The FDA must cease and desist any and all promotion of the mRNA gene vaccine for COVID.

All senior officials of FDA must be removed and re-assigned to other agencies. 25% of the FDA’s workforce must be fired within 2 months of the new FDA Commissioner taking office.

FDA must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies or decisions, advisory boards etc.

FDA is to take no funding or donations or financial support of any kind from any pharmaceutical industry parties etc.

FDA must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.

The new FDA Commissioner under Trump 2.0 must work with head agency HHS Secretary and CDC and NIH etc. to reverse the 1986 Childhood vaccine ACT; National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was signed into law by United States President Ronald Reagan; NCVIA's purpose was to eliminate the potential financial liability of vaccine manufacturers due to vaccine injury claims; so that anyone harmed in the future by vaccines can sue the vaccine makers and all involved

The new FDA Commissioner under Trump 2.0 must work with head agency HHS Secretary and CDC and NIH etc. to end and make retroactive the LIABILITY PROTECTION under PREP Act that Azar helped implement (Feb/March 2020) and enforce/activate for the fraud PCR manufactured COVID; this so that those harmed by the mRNA vaccine can enter courts for financial redress.

The new FDA Commissioner under Trump 2.0 must make available to the public all data related to COVID, all, all linked to the mRNA vaccines that FDA, CDC, NIH etc. has in possession. Bourla, Bancel etc. All.

The new FDA Commissioner under Trump 2.0 with CDC, HHS etc. must work immediately with POTUS Trump to end the woke TRANSGENDER madness and brutal transgender surgeries and puberty blockers on our children.

The new FDA Commissioner under Trump 2.0 must work with head agency HHS Secretary and CDC and NIH etc. to set up a victim compensation fund for all those hurt by the COVID fraud OWS lockdowns and the Malone et al. mRNA vaccine.

FDA Commissioner must examine each unit, department, entity under its purview and if a duplication or a waste of tax-payer money, if not a functional high-quality entity within FDA, then it must be shut down. Top level technocrats must be removed, reassigned and if possible, cut 25% of all staff across the board. This examination must begin on the first day of being sworn in as the new head.

CDC

3)The CDC must immediately disband the MMWR (Morbidity and Mortality Weekly Report) it produces (especially during COVID) given its lack of scientific rigor, merit, substance and the politicization of the MMWR. This may be replaced by an independent, unbiased public health report.

The CDC must cease and desist any and all promotion of the mRNA technology gene vaccine for COVID.

CDC Director (incoming) must commit to end the revolving door between itself and BIG Pharma, that he himself/herself will accept no position within BIG Pharma for at least 5 years post leaving the CDC position.

All senior officials of CDC must be removed and re-assigned to other agencies. 25% of the CDC’s workforce must be fired within 2 months of the new CDC Director taking office.

The CDC must immediately disband the VAERS vaccine adverse event database surveillance system and replace it with an updated acute surveillance system to track and report on mRNA vaccine harms and deaths with a focus on the upcoming 25 years.

CDC must immediately stop all gain-of-function (GoF) or related research in any US affiliated or funded or operated biolab anywhere in the world. CDC must stop its involvement (direct or indirectly) all bioweapons biological research in US laboratories and anywhere globally that the US is affiliated to. No US tax-payer money must be used for any such research anywhere in the world.

CDC must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies or decisions, advisory boards etc.

CDC is to take no funding or donations or financial support of any kind from any pharmaceutical industry parties etc.

CDC must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.

CDC Director must examine each unit, department, entity under its purview and if a duplication or a waste of tax-payer money, if not a functional high-quality entity within CDC, then it must be shut down. Top level technocrats must be removed, reassigned and if possible, cut 25% of all staff across the board. This examination must begin on the first day of being sworn in as the new head.

NIAID

4)NIAID must immediately stop all gain-of-function (GoF) or related research in any US affiliated or funded or operated biolab anywhere in the world. NIAID must stop its involvement (direct or indirectly) all bioweapons biological research in US laboratories and anywhere globally that the US is affiliated to. No US tax-payer money must be used for any such research anywhere in the world. NIAID must return to the 1972/1975 Nixon era and agreements (1969 to 1976 Nixon era, the Biological Weapons Convention (BWC), or Biological and Toxin Weapons Convention (BTWC) 1975 relating to weapons of mass destruction) and renounce the use of lethal biological agents and weapons, and all other methods of biological warfare. Renounce its role in such lethal biological agents and weapons. NIAID will confine its biological research to defensive measures such as immunization and safety measures and work with the Department of Defense in disposing of existing stocks of bacteriological or any such weapons or specimens. The same posture for NIAID in use or research in and of lethal chemical weapons.

NIAID must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies or decisions, advisory boards etc.

NIAID is to take no funding or donations or financial support of any kind from any pharmaceutical industry parties etc.

NIAID Director must examine each unit, department, entity under its purview and if a duplication or a waste of tax-payer money, if not a functional high-quality entity within NIAID, then it must be shut down. Top level technocrats must be removed, reassigned and if possible, cut 25% of all staff across the board. This examination must begin on the first day of being sworn in as the new head.

NIAID must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.

___

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