6.5.2025 | 10:49
Supplementary Submission to the Parliamentary Ombudsman of Iceland
May 5, 2025
Parliamentary Ombudsman of Iceland
Kristķn Benediktsdóttir
Laugavegur 116
101 Reykjavķk, Iceland
Subject: Supplementary Submission Regarding Public Health Measures and Vaccination Program 20202023
With this supplementary submission, building on my previous submission dated April 18, 2025, I request an investigation into the administrative practices of Icelandic authorities concerning public health measures and the vaccination program from 2020 to 2023. Data indicate unreasonable harm, including an 83.9% increase in infant mortality in 2021, a 30.5% excess mortality in 2022, and a 15.0% decline in births from 2021 to 2023 (Statistics Iceland 2021, 2024, 2025), alongside a severe lack of transparency and informed consent (Appendix: Summary of Public Health Measures and Covid-19 Vaccinations in Iceland 20202023, Chapters 2, 3). The international context, including the secrecy of pharmaceutical company data and the role of DoD/DARPA, underscores the gravity of the matter (Appendix, Chapter 1), although this falls outside the jurisdiction of your office. This submission focuses on the responsibility of Icelandic authorities and potential violations of Icelandic laws and international ethical standards. Copies of this submission will be sent to the Welfare Committee of the Icelandic Parliament, the Icelandic Human Rights Institute, and independent Icelandic media to ensure broad review.
1. Scientific Basis and Administration
Public health measures, supported by the Communicable Diseases Act (No. 19/1997, amendments No. 99/2020, 100/2020), were partly based on unreliable RT-PCR tests (Ct 35-40; false positive rate 97.499.9%; Robert Koch Institute 2020; WHO 2021) and limited scientific data (Appendix, Chapters 1, 2). Restrictions on freedom of movement, social life, and economic activity were often justified without confirmed studies on effectiveness (Jefferson et al. 2023; Ioannidis 2020). I request an investigation into how Icelandic authorities justified these measures and whether sufficient oversight of the scientific basis was ensured.
2. Transparency and Agreements with Pharmaceutical Companies
The agreement between Icelandic authorities and pharmaceutical companies was neither presented to the Icelandic Parliament for full discussion nor submitted to the Scientific Ethics Committee, which may violate the Medicines Act No. 93/1994 and the Constitution (Article 51 on the role of Parliament; Appendix, Chapter 3). Data from Pfizer reveal serious adverse effects of Process 2 mRNA vaccines, including >1,223 deaths (Dec. 2020Feb. 2021), which were concealed until Judge Pittman ordered their release (PHMPT v. FDA 2022; Appendix, Chapter 1). I request an investigation into whether Icelandic authorities ensured transparency and oversight of agreements and vaccines, and whether the lack of submission to the Scientific Ethics Committee violates Icelandic law.
3. Knowledge and Responsibility of the Icelandic Medicines Agency
Data on adverse effects of mRNA vaccines, including immunosuppression and increased infections (Pfizer Inc. 2021; Cleveland Clinic 2022), were accessible to international regulatory bodies, including the EMA, with which the Icelandic Medicines Agency (IMA) collaborates (Appendix, Chapter 2). I request an investigation into whether the IMA and the Ministry of Health fulfilled their oversight duties under the Medicines Act No. 93/1994, and why the vaccination program continued without further safety studies in light of evidence of harm, such as the 83.9% increase in infant mortality (Statistics Iceland 2021; Appendix, Chapter 2).
4. Human Rights and Ethical Violations
The lack of informed consent for vaccinations, combined with restricted access to data, violates the Patients Rights Act No. 74/1997, the Constitution (Articles 67, 71), the Helsinki Declaration (WMA 2013), and the Nuremberg Code (IMT 1945; Appendix, Chapter 3). The Health Directorates denial of access to data (Jan. 2024) violates the Information Act No. 140/2012 (Appendix, Chapter 4). I request an investigation into whether Icelandic authorities ensured citizens rights and whether these violations warrant further review on an international level, e.g., by the European Court of Human Rights (ECHR).
5. Severe Harm and Need for Investigation
Data indicate unreasonable harm, including an 83.9% increase in infant mortality in 2021, a 15.0% decline in births from 2021 to 2023 (Statistics Iceland 2021, 2024), and a 66% decline in births among vaccinated women in the Czech Republic (SMIS 2024; Appendix, Chapter 2). Studies suggest potential biological effects of mRNA vaccines (McKernan et al. 2025; Iwasaki et al. 2025). I request an investigation into whether Icelandic authorities assessed these anomalies, ensured independent analysis of the long-term effects of vaccines, and whether the continued use of mRNA vaccines aligns with Icelandic laws and ethical standards.
Demands
- An investigation into the administrative practices of Icelandic authorities regarding transparency, informed consent, and the scientific basis of public health measures and the vaccination program 20202023.
- An investigation into the agreement with pharmaceutical companies, which was not presented to Parliament or the Scientific Ethics Committee, and whether it violates the Medicines Act No. 93/1994 and the Constitution.
- An investigation into whether the Icelandic Medicines Agency (IMA) and the Ministry of Health fulfilled their oversight duties in light of data on adverse effects.
- Access to data on agreements with pharmaceutical companies and adverse effects of vaccines, in accordance with the Information Act No. 140/2012.
- An assessment of whether severe harm and violations of citizens rights warrant an independent investigation, potentially at an international level, e.g., by the European Court of Human Rights (ECHR), and whether immediate suspension of mRNA vaccinations is necessary in light of evidence of harm (Appendix, Chapter 2).
Closing Remarks
Data suggest unreasonable harm from the vaccination program 20202023, alongside a severe lack of transparency and accountability (Appendix, Chapters 2, 3). The international context, including the secrecy of pharmaceutical data and flawed studies under DoD/DARPA oversight, sheds light on the seriousness of the matter (Appendix, Chapter 1). I request an investigation into the responsibility of Icelandic authorities, with a focus on potential violations of the Patients Rights Act No. 74/1997, the Medicines Act No. 93/1994, and international ethical standards, to ensure justice and public trust in the authorities.
Respectfully,
Gušmundur Karl Snębjörnsson, MD
World Council for Health Iceland
X: @KalliSnae
Facebook: Kalli Snę
Blog: https://kallisnae.blog.is
Copies sent to:
Welfare Committee of the Icelandic Parliament
Leaders of Political Parties
Icelandic Human Rights Institute
Ombudsman for Children
Icelandic Media
Copies of the supplementary submission and appendix in English:
World Council for Health
Independent Medical Alliance
North Group
European Court of Human Rights (ECHR)
Childrens Health Defense
_______________________________________________________________________________________
Appendix:
Summary of Public Health Measures and Covid-19 Vaccinations in Iceland 20202023.
Public Health Laws 20202023, Distorted Science, and Related Issues
This summary aims to analyze the overall picture of public health measures in Iceland and internationally from 2020 to 2023, categorized into political, medical, legal, ethical/philosophical, and media influence in support of government actions, with a focus on scientific basis, transparency, and ethical considerations.
1. Political Decision-Making Process
Key Points:
- The Communicable Diseases Act (No. 19/1997, amendments No. 99/2020, 100/2020) authorized restrictions, including social distancing, isolation, mask mandates, travel restrictions, and lockdowns, but the scientific basis was limited, often relying on models and wishful thinking rather than confirmed studies, e.g., due to insufficient evidence on the effectiveness of mask mandates (Jefferson et al. 2023), social distancing (Ioannidis 2020), isolation (Allen et al. 2022; Nussbaumer-Streit et al. 2020), travel restrictions (Burns et al. 2021), and lockdowns (Herby et al. 2022; Chin et al. 2021).
- RT-PCR tests (Ct 35-40, 97.499.9% false positives) were unreliable, used to justify unlawful quarantine (Robert Koch Institute 2020; WHO 2021).
- Civil protection authorities exaggerated the COVID-19 threat, dismissing critical perspectives (Snębjörnsson 2025a; Desmet 2022).
- HHS/Pfizer secrecy: Pfizer data show Process 2 mRNA vaccines lacked efficacy, caused immunosuppression, >1,223 deaths (Dec. 2020Feb. 2021), and were used without emergency authorization (Pfizer Inc. 2021). HHS/Pfizer sought 75-year secrecy, but Federal Judge Pittman ordered disclosure on Jan. 6, 2022 (PHMPT v. FDA 2022).
- DoD/DARPA and pharmaceutical companies: DARPA oversaw mRNA development since 2011 (ADEPT, P3), with Pfizer/Moderna as subcontractors under OTA agreements (STAT News 2020; Schoeni 2023). The Jackson case (United States v. Ventavia Research Grp., 2023) confirms DoD/DARPA liability, with Pfizer as a subcontractor exempt from FDA regulations (UncoverDC 2022; NTD 2023). Judge Truncale dismissed the case on Aug. 9, 2024, on the grounds that DoD, not Pfizer, was the responsible party (Childrens Health Defense 2024). Operation Warp Speed (OWS) ensured rapid market entry (The Washington Post 2020).
- Excess deaths (30.5% in 2022, 6-Sigma) rule out natural causes (Statistics Iceland 2025).
Conflicts of Interest:
- Pfizer/Moderna earned billions (Hammond et al. 2024).
- DoD/DARPA contracts supported military interests (STAT News 2020).
Conclusion: Political decisions, backed by DoD/DARPA, relied on unreliable RT-PCR tests and concealed data, suggesting intentional misconduct.
2. Medical Decisions and Scientific Integrity
Key Points:
- PCR Tests: Unreliable RT-PCR tests (Ct 35-40) inflated case numbers, supported by the Robert Koch Institute (2020), and justified unlawful quarantine (WHO 2021; Borger et al. 2021).
- mRNA Vaccines: Process 2 (E. coli-based, SV40 promoter) was used without authorization, violating the Medicines Act No. 93/1994 (McKernan et al. 2023). Pfizer data show >1,223 deaths, 80% miscarriages, immunosuppression, and increased infections (Pfizer Inc. 2021; Cleveland Clinic 2022). Adverse effects include heart attacks (+20.22%) (Statistics Iceland 2025).
- Infant Mortality in Iceland 2021: An 83.9% increase in total deaths from 28 weeks gestation to 28 days post-birth compared to the 20152019 average (3.1 per 1,000; 2020: 3.1 per 1,000; 2021: 5.7 per 1,000, 28 cases), the highest rate since 1988 (Statistics Iceland 2021). The timing aligns with the vaccination of pregnant women (springsummer 2021), though Statistics Iceland does not provide direct causation, and data do not allow breakdown by nationality (21% born to women with foreign citizenship in 2021). Further investigation is needed to confirm potential links to mRNA vaccines.
- Births in Iceland 20212023: A 15.0% decline in live births from 2021 (4,879) to 2023 (4,146) (Statistics Iceland 2024).
- Births in the Czech Republic 2023: A 66% decline among vaccinated women aged 1839 (unvaccinated: 114 per 1,000; vaccinated: 42 per 1,000, odds ratio 0.34), an unusual drop (SMIS 2024; Rates of Successful Conceptions 2025). The timing correlates with conceptions in 2022, when 68% of women were vaccinated.
- Fertility in Iceland: Dropped from 2.1 (2012) to 1.59 (2025), a 24% decline, indicating population decline (Statistics Iceland 2025).
- Studies: McKernan et al. (2025) suggest TENT5A re-adenylation in mRNA vaccines may affect fetal development. Iwasaki et al. (2025) detect spike protein in vaccinated individuals bodies for over 700 days, indicating long-term fertility impacts.
- Remdesivir: 53% mortality rate (Mulangu et al. 2019). Used at Icelands National University Hospital despite lack of efficacy and significant harm (WHO 2020).
- DoD/DARPA Oversight: DARPA developed mRNA technology (ADEPT 2011, P3 2016), with Pfizer/Moderna as subcontractors without adequate safety studies (STAT News 2020). The Jackson case reveals flawed studies, exempt from FDA regulations, with DoD liability (NTD 2023; BMJ 2021; Childrens Health Defense 2024).
- Excess Deaths: 519 deaths in 2022 (30.5%, 6-Sigma), 2,000 over 20202023 (Statistics Iceland 2025).
Scientific Integrity:
- Studies on Process 2 were inadequate and lacked emergency authorization, though Process 1 received such approval but was not used in vaccinations; the placebo group was eliminated, limiting safety assessment (Pfizer Inc. 2020; Guetzkow 2022; PHMPT v. FDA 2022).
- VAERS recorded over 1 million adverse events, and excess deaths in Iceland (30.5% in 2022, 6-Sigma) indicate severe harm (icandecide.org 2021; Statistics Iceland 2025).
Conclusion: Medical decisions, under DoD/DARPA oversight, relied on flawed science, supported by an 83.9% increase in infant mortality and a 15.0% decline in births, necessitating further investigation.
3. Human Rights and Legal Considerations
Key Points:
- Icelandic Law: Process 2 violates the Medicines Act No. 93/1994. Lack of informed consent violates the Patients Rights Act No. 74/1997. Denial of access to data violates the Information Act No. 140/2012. Restrictions on freedom of movement, lockdowns, isolation, and secrecy violate the Constitution (Articles 67, 71, 65, 73, 75).
- International Agreements: Violations of the Helsinki Declaration (1964, revised 2013), Articles 5, 6, 8, requiring informed consent, transparency, and risk minimization in medical research (WMA 2013). mRNA vaccines, used without adequate safety data and under secret OTA agreements, breach these principles. Violations of the Nuremberg Code (IMT 1945), Rule 1 (voluntary consent) and Rule 7 (avoid unnecessary risk), due to lack of transparency and inadequate studies. Violations of the European Convention on Human Rights (ECHR) (Articles 2, 5, 8, 10) and the International Covenant on Civil and Political Rights (ICCPR) (Articles 6, 7, 9) regarding the right to life, liberty, and prohibition of medical experimentation without consent.
- HHS/Pfizer Secrecy: A 75-year secrecy request violates the Freedom of Information Act (FOIA) (1967) (PHMPT v. FDA 2022).
- DoD/DARPA and Jackson Case: OTA agreements exempted Pfizer from FDA regulations, obstructed transparency, and prevented informed consent (UncoverDC 2022; NTD 2023). Judge Truncale (2024) confirmed DoD liability, violating the Helsinki Declaration and Nuremberg Code (Childrens Health Defense 2024).
Conclusion: Actions, backed by DoD/DARPA, violated Icelandic law, the Helsinki Declaration, the Nuremberg Code, and international agreements (ECHR, ICCPR) due to lack of informed consent, transparency, and legality, necessitating further review.
4. Media Influence and Censorship
Key Points:
- Media exaggerated fear, marginalized skeptics, and supported one-sided government narratives (Snębjörnsson 2025a; Desmet 2022).
- The Health Directorates denial of access to data (January 2024) violates the Information Act No. 140/2012.
- Media suppressed DoD/DARPAs role (X posts 2024).
Conclusion: Media obstructed transparency through one-sided coverage and support for government actions, calling for scrutiny of their impact on public opinion.
5. Ethical and Philosophical Considerations
Key Points:
- Intent: Evidence suggests intentional misconduct (democide), supported by Pfizer data, 75-year secrecy, DoD/DARPA liability, an 83.9% increase in infant mortality, a 15.0% decline in Icelandic births, a 66% decline among vaccinated women in the Czech Republic, and 6-Sigma harm (Pfizer Inc. 2021; PHMPT v. FDA 2022; OSAPG 1948).
- Ethics: Use of Process 2 without informed consent, under DoD/DARPA oversight, violates the Helsinki Declaration (Article 8, risk minimization) and the Nuremberg Code (Rule 1, voluntary consent) (WMA 2013; IMT 1945).
- Philosophy: Mass formation, as described by Desmets theory of mass formation psychosis (2022), fueled fear and compliance with measures due to one-sided narratives and social pressure, supported by psychological theories of Jung (1964) and Arendt (1951) on group behavior in crises.
Conclusion: Ethical violations, enabled by military oversight and mass formation, made harm possible, calling for ethical scrutiny.
6. Overall Conclusion
Key Points:
- Public health measures from 2020 to 2023 were significantly based on distorted science and limited scientific evidence.
- Unreliable RT-PCR tests (Ct 35-40, 97.499.9% false positives) were used to justify unlawful quarantine (Robert Koch Institute 2020; WHO 2021). Restrictions, including social distancing, isolation, mask mandates, travel restrictions, and lockdowns, had limited scientific basis, often relying on models and wishful thinking rather than confirmed studies (Jefferson et al. 2023; Ioannidis 2020; Allen et al. 2022; Burns et al. 2021; Herby et al. 2022; Nussbaumer-Streit et al. 2020; Chin et al. 2021).
- Pfizer data, initially concealed for 75 years, show that Process 2 mRNA vaccines lacked efficacy, caused immunosuppression, and led to >1,223 deaths (Dec. 2020Feb. 2021), but Judge Pittman ordered disclosure (PHMPT v. FDA 2022).
- The Brook Jackson case confirms DoD/DARPA liability for mRNA development, with Pfizer as a subcontractor (United States v. Ventavia Research Grp., 2023; NTD 2023). Judge Truncale dismissed the case (Aug. 9, 2024), affirming DoD liability (Childrens Health Defense 2024).
- Infant mortality in Iceland in 2021 increased by 83.9% (from 3.1 to 5.7 per 1,000), and births declined by 15.0% from 2021 to 2023 (Statistics Iceland 2024).
- Births among vaccinated women in the Czech Republic in 2023 dropped by 66% (SMIS 2024).
- Fertility in Iceland fell by 24% (from 2.1 to 1.59, 20122025), indicating population decline (Statistics Iceland 2025).
- McKernan et al. (2025) and Iwasaki et al. (2025) suggest biological effects of mRNA vaccines on fetal development and fertility.
- Excess deaths (30.5% in 2022, 6-Sigma) are linked to vaccines (Statistics Iceland 2025).
- Measures violated Icelandic law (Constitution, Acts No. 93/1994, 74/1997), the Helsinki Declaration (informed consent, transparency), the Nuremberg Code (voluntary consent), and international agreements (ECHR, ICCPR).
- Media concealed DoD/DARPAs role.
- Mass formation fueled societal fear (Desmet 2022).
- Evidence of intentional misconduct (democide) is supported by secrecy, harm, and military interests.
Demands:
- An independent investigation into DoD/DARPA liability, Process 2, excess mortality, infant mortality, birth decline, and biological effects of mRNA vaccines.
- Consideration of a potential complaint to the European Court of Human Rights (ECHR) and the United Nations (UN).
- Disclosure of data on DARPA agreements and adverse effects.
- The necessity to halt further mRNA vaccinations.
References
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Respectfully,
sign
Gušmundur Karl Snębjörnsson, MD
World Council for Health Iceland
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