Katherine Watt on Baliwick News:

I’m not a lawyer. I’m a paralegal and writer.

I do legal research and writing to support civil and criminal cases brought in American courts, and to educate and mobilize more people to exert social and political pressure on federal and state legislators, prosecutors and judges, to terminate the interlocking control-and-cull campaigns operated under a fraudulent national emergency framework; hold accountable the US Government officials who pseudo-authorize, actually-fund, and run the programs; and set up relief programs for injured victims and survivors of the dead.

Written/compiled by Katherine Watt, this timeline was published on 19 Dec 2022: Biomedical security state and state-run bioterrorism programs: six American statutory frameworks. 14-page summary: nine pages of text with five pages of endnotes. (14-page PDF). It begins with:

LEGAL HISTORY – AMERICAN DOMESTIC BIOTERRORISM PROGRAM
Enabling statutes, regulations, executive orders, guidance documents and budget allocations.

 

At least six Congressionally-authorized statutory frameworks and related budget appropriations, reinforced through Presidential Executive Orders and related executive branch declarations,[1] and implemented through hundreds of regulatory amendments,[2] mostly promulgated through the Federal Register since 1969, authorized and funded a coordinated US Government attack (actors), on the American people (targets), using toxic biological and chemical material (bioagents/biochemical weapons) distributed across state borders labelled as “Covid-19 vaccines.”[3]

These biochemical weapons have been fraudulently marketed by the US Government and pharmaceutical weapons manufacturers including Pfizer, Moderna, Johnson & Johnson and their manufacturing subcontractors as “safe and effective vaccines,” following the transfer of the US Government’s Chemical and Biological Warfare Program, formerly housed in the Department of Defense (DOD), to the Public Health Emergency (PHE) Emergency Use Authorization (EUA) Medical Countermeasures (MCM) program.­

The American chemical and biological warfare program is now housed in the Department of Health and Human Services (HHS) and jointly operated by DOD, HHS, Department of Homeland Security, Department of State, most other federal agencies and their subordinate departments, divisions, offices, authorities, enterprises, committees, advisory boards and employees.

Six of the enabling statutes, in chronological order of Congressional enactment:

1 1983-present, relevant Presidential Executive Orders, proclamations and related acts, partial list: Executive Order 12452, 1983 (expanded list of communicable diseases subjecting citizens to forcible apprehension and detention under HHS Secretary quarantine authority); EO 13139, 1999 (forced experimental, unapproved ‘vaccines’ on armed forces without informed consent); Proclamation 7463, 2001 (Declaration of National Emergency by Reason of Certain Terrorist Attacks, renewed annually since); EO 13295, 2003 (added symptomatic SARS to quarantinable communicable diseases); EO 13375, 2005 (added symptomatic influenza to quarantinable communicable diseases; National Security Presidential Directive 51, 2007; EO 13527, 2009 (Establishing Federal Capability for the Timely Provision of Medical Countermeasures Following a Biological Attack); EO 13601, 2012 (National Defense Resources Preparedness); EO 13674, 2014 (added asymptomatic, suspected SARS to quarantinable communicable diseases); EO 13747, 2016 (Advancing the Global Health Security Agenda to Achieve a World Safe and Secure from Infectious Disease Threats); EO 13887, 2019 (Modernizing Influenza Vaccines in the United States to Promote National Security and Public Health; directed rapid-deployment mRNA/DNA/LNP/nanotech drugs and devices); Proclamation 9994, 2020 (Declaring a National Emergency Concerning the Novel Coronavirus Disease (COVID-19) Outbreak, renewed annually since); EO 13909, 2020 (Prioritizing and Allocating Health and Medical Resources to Respond to the Spread of COVID-19): EO 13910, 2020 (Preventing Hoarding of Health and Medical Resources To Respond to the Spread of COVID-19); EO 13911, 2020 (Delegating Additional Authority Under the Defense Production Act With Respect to Health and Medical Resources To Respond to the Spread of COVID-19); EO 14047, 2021 (added measles to the list of quarantinable communicable diseases); EO 14081, 2022 (Advancing Biotechnology and Biomanufacturing Innovation for a Sustainable, Safe, and Secure American Bioeconomy.)

2 1981-present, relevant HHS Proposed Rules, Final Rules, Notices, and Guidance for Industry, partial list: HHS-Food and Drug Administration Final Rule Protections for Human Subjects; Prisoners Used as Subjects in Research (1981); HHS-FDA Final Rule Protection of Human Subjects; Informed Consent (1981); HHS Interim Final Rule: Informed Consent for Human Drugs and Biologics; Determination that Informed Consent is Not Feasible (1990); 1991 Common Rule (1991); HHS-FDA Guidance for Human Somatic Cell Therapy and Gene Therapy (1998); HHS Interim Final Rule – Human Drugs and Biologics; Determination That Informed Consent Is NOT Feasible or Is Contrary to the Best Interests of Recipients; Revocation of 1990 Interim Final Rule; Establishment of New Interim Final Rule (1999); HHS-FDA Draft Guidance Re: Emergency Use Authorization of Medical Products (2005); HHS-FDA Interim Final Rule, Medical Devices; Exception From General Requirements for Informed Consent (2006) HHS-FDA Guidance: Gene Therapy Clinical Trials – Observing Subjects for Delayed Adverse Effects (2006); HHS-FDA Guidance – Emergency Use Authorization of Medical Products (2007); HHS Interim Final Rule – FDA Exceptions or Alternatives to Labeling Requirements for Products Held by the Strategic National Stockpile. (2007); HHS-FDA Final Rule: Medical Devices; Exception From General Requirements for Informed Consent (2011); HHS-FDA Guidance: Potency Tests for Cellular and Gene Therapy Products (2011); HHS-FDA Preclinical Assessment of Investigational Cellular and Gene Therapy Products (2013); HHS-FDA Guidance: Decisions for Investigational Device Exemption Clinical Investigations (2014); HHS-FDA Considerations for the Design of Early-Phase Clinical Trials of Cellular and Gene Therapy Products (2015); HHS-FDA Guidance: Design and Analysis of Shedding Studies for Virus or Bacteria-Based Gene Therapy and Oncolytic Products (2015); HHS Final Rule – HHS Clinical Trials Registration and Results (2016); HHS Workshop Summary – The Nation’s Medical Countermeasure Stockpile: Opportunities to Improve the Efficiency, Effectiveness, and Sustainability of the CDC Strategic National Stockpile (2016); HHS-FDA Guidance: Emergency Use Authorization of Medical Products and Related Authorities (2017); HHS Final Rule – Federal Policy for the Protection of Human Subjects (2017); HHS Final Rule – Control of Communicable Diseases (2017); HHS-FDA Guidance: IRB Waiver or Alteration of Informed Consent for Clinical Investigations Involving No More Than Minimal Risk to Human Subjects (2017); HHS-FDA Guidance: Use of Real-World Evidence to Support Regulatory Decision-Making for Medical Devices (2017); HHS Final Rule – Federal Policy for the Protection of Human Subjects: Six Month Delay of the General Compliance Date of Revisions While Allowing the Use of Three Burden-Reducing Provisions During the Delay Period (2018); HHS-FDA Guidance: Development and Licensure of Vaccines to Prevent COVID-19 (2020); HHS-FDA Guidance: Emergency Use Authorization for Vaccines to Prevent COVID-19 (2020); HHS-FDA Guidance: Real-World Data – Assessing Electronic Health Records and Medical Claims Data To Support Regulatory Decision-Making for Drug and Biological Products (2021); HHS-FDA Guidance: Real-World Data – Assessing Registries to Support Regulatory Decision-Making for Drug and Biological Products (2021); HHS Interim Final Rule – Possession, Use, and Transfer of Select Agents and Toxins–Addition of SARS-CoV/SARS-CoV-2 Chimeric Viruses Resulting From Any Deliberate Manipulation of SARS-CoV-2 To Incorporate Nucleic Acids Coding for SARS-CoV Virulence Factors to the HHS List of Select Agents and Toxins (2021); HHS Final Rule – National Vaccine Injury Compensation Program: Adding the Category of Vaccines Recommended for Pregnant Women to the Vaccine Injury Table (2022); HHS-FDA Proposed Rules: Protection of Human Subjects and Institutional Review Boards (2022)

32018: “Agent or bioagent is used broadly to refer to any product created using biological components that may be intended to cause harm. In the context of synthetic biology, an agent could be a pathogen, a toxin, or even a biological component, such as a genetic construct or a biochemical pathway, that may be developed with the intent to harm a human target; Actor is used to refer to individuals or groups who may seek to effect an attack; Target is typically used to refer to the human beings harmed (or intended to be harmed) in an attack. In the context of manipulation of biological components, target may be used to refer to the intended outcomes of those manipulations.” Biodefense in the Age of Synthetic Biology, National Academy of Sciences (2018).

This summary—referenced in Orientation for new readers, text and video links—is one in a list of five documents covering U.S. Legal History of leading up to today.

Collapsologie Eugenics + Bioweapons + Big Pharma False Enemy Fear Campaigns Mind Control--Psy Ops--Propaganda--and Disinformation Rise of Fascism US Intelligence Agencies