REIMAGINING REGULATION FOR THE AGE OF ARTIFICIAL INTELLIGENCE (AI) PROJECT- NZ GOVERNMENT PARTNERING THE WORLD ECONOMIC FORUM
Precision Farming is also known as Smart Farming. Smart Farming like Smart Cities include significantly increased surveillance, monitoring of every aspect of your life.

Surveillance of non-humans and humans, the dual purpose of Smart Farming. Which leads to zilch freedom, your private life being highly monitored hence controlled by digital technology through Precision Farming/ Smart Farming.

‘Smart is increasingly a euphemism for surveillance. Cities in at least 56 countries worldwide have deployed surveillance technologies powered by automatic data mining, facial recognition, and other forms of artificial intelligence.
Urban surveillance is a multi-billion dollar industry, with Chinese and U.S.-based companies such as Axis, Dahua, Hikvision, Huawei, and ZTE leading the charge.

Now digital totalitarianism goes rural. Thus supercharging surveillance, encroaching on free speech, privacy, and data protection.
Identity collection devices are commonplace, having exploded across public and private spaces. Shanghai recently installed Alibaba’s City Brain public surveillance system, which oversees over 1,100 biometric facial recognition cameras. A combination of satellites, drones, and fixed cameras grab over 20 million images a day.

The bus, metro, and credit cards of local residents are also traced in real time. And these tools are spreading. Chinese firms are busily exporting surveillance tech to Latin America, other parts of Asia, and Africa, helping enable what some critics call digital authoritarianism.

New Zealand Government has its surveillance strategy as to COVID 19 monitoring. Public Health Surveillance of public health and data.
New Zealand surveillance data provided by ESR, funded by the Ministry of Health with the cooperation of the diagnostic laboratories.

Ministry of Health support enables ESR to provide some specific additional work, prioritised on the basis of national benefit and we are happy to collaborate with funded projects to mine the surveillance data. How transparent is this and how private?

The new coronavirus pandemic and related lockdown measures triggered a significant increase in digital control over people in many countries.
Search your history books how totalitarianism has caused torture, famines, millions murdered, imprisoned through Totalitarian Dictatorships. Under Digital Global Inclusion is our individual uniqueness being annihilated, is Newland as a sovereign nation being annihilated deliberately so, to replace, denounce NZ Citizenship for Global Citizenship?

Farming is the backbone of New Zealand, it’s credible to question , is this White Paper Project that refers to the NZ Governments partnership with the World Economic Forum part of the Global Digital Playbook to destroy the backbone of New Zealand through Smart Cities, Smart Farming (Precision Farming)?

Wake Up New Zealand. Carol Sakey.
PLEASE GO TO THE ARROW ABOVE THAT WILL LINK YOU TO MY RUMBLE VIDEO TO MORE IMPORTANT INFORMATION ON NZ GOVERNMENTS PARTNERSHIP WHITE PAPER WITH THE WORLD ECONOMIC FORUM.

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Behind the closed doors of the political toilet bowl of Wellington the New Zealand Government is reaping its global glory as it promotes, makes plans and policies partnering with Google AI and the World Economic Forum and its UN official partnership with the UN.
International laws to control the planet, people and profit. The wealthy 0.01% of wealthy multistakeholder capitalist corporations, big tech, big pharma, Bayers-Monsanto GE seeds, Lab manufactured foods. A system, digital framework on a one global metric system that includes the now COVID19 restrictions right into year 2030.

The destruction of the world economy through COVID19 controls, restrictions – a window of opportunity to redesign your life, your diet the way you think, behave – live. The Government calls this ‘Unlocking New Zealand’s Digital Potential’. More censorship, more surveillance, trading privacy for security. A global Digital transformation…leave no-one behind, everyone, everywhere at every age. From the cradle to the grave.
Everyone monitored, controlled by a Communist Chinese Social Credit System, rewards and punishments. Comply – don’t comply you lose your freedoms. Using the bludgeoning of fear to control the people. (Fear is a liar).

Legal Fictions are rife through data in and data out, global metric systems, data modelling biases, predictions. Real Science is under attack. Real history is under attack. The citizens of New Zealand are under attack. Free Speech is under attack.

To learn more about this please go to my Rumble Video link in the image above, Thank you.

How will Medsafe assess the short and long-term efficacy and/or safety of a COVID-19 vaccine?

Medsafe will apply its usual assessment criteria for the evaluation of any COVID-19 vaccine submissions. We will use international regulatory guidance in general, and advice specific to COVID-19 vaccines.

Efficacy is determined by the results of clinical trial(s) and studies on the types of immune response generated by the vaccine.
Safety data will be available from the clinical trials. As for all medicines, additional safety information will be gathered from long-term follow-up of clinical trial participants and safety monitoring.

Most information provided to Medsafe as part of a medicine application is confidential to the pharmaceutical company. However, some detail such as the qualitative product formulation, site of manufacture, and the data sheet will be published on Medsafe website when the vaccine is approved
How long will the vaccines work?

At this stage, we do not know how long a vaccine might work for.

Where can I find the clinical, safety, and quality data that Medsafe evaluated to approve COVID-19 vaccines?
Information submitted to and held by Medsafe as part of the approval process is confidential to the respective pharmaceutical companies
Provisional consent allows conditions to be imposed on the vaccine, restricting its use by healthcare professionals according to the data available at the time of approval. Provisional consent was included in the Medicines Act to allow New Zealand patients to have early access to medicines with a significant unmet clinical need.

What happens when the provisional consent for a COVID-19 vaccine expires?
Provisional consent was granted to all three currently approved COVID-19 vaccines for a period of nine months. Prior to expiry of this period, provisional consent may be renewed for a further period of up to two years, full consent may be granted, or the consent may not be renewed.
Medsafe has renewed the provisional consent for Comirnaty for a period of two years and the renewed consent is valid until 3 November 2023.
COVID-19 Vaccine Safety – Questions and Answers PUBLISHED 27TH November 2021 MEDSAFE WEBSITE https://www.medsafe.govt.nz/COVID-19/q-and-a-vaccine-safety.asp

PLEASE NOTE:-Should I be getting a COVID-19 vaccine while I am pregnant?
Currently, the Comirnaty (Pfizer) vaccine is the only COVID-19 vaccine available in New Zealand. There is limited data with the use of Comirnaty in pregnant women. Animal studies have not indicated direct or indirect harmful effects in pregnancy, development of the fetus or the newborn.

WHAT ADVERSE EVENTS AFTER JABS ARE- doctors, nurses, DHB staff, pharmacists required to report to the Centre for Adverse Reactions Monitoring (CARM)?
There is no legal requirement for healthcare professionals to report adverse events following immunisation (AEFIs). However, we encourage healthcare professionals to report all AEFIs

ARE ADVERSE EVENTS OCCCURRING within a specified period after vaccination required to be reported to CARM?
There is no time limit for reporting adverse events.
Are adverse events listed by the vaccine manufacturer in the package inserts and data sheets required to be reported to CARM?
There is no legal requirement to report adverse events.

DOES THE JAB AFFECT FERTILITY:- Animal studies for the Comirnaty vaccine did not show any effect on fertility.

ARE THE COVID JABS SAFE FOR CHILDREN?..The Comirnaty vaccine is indicated for use in individuals aged 12 years and older. Clinical trials to assess safety and efficacy in children are ongoing.

WHAT MEDSAFE STUDIES HAVE MEDSAFE DONE.. to ensure the vaccine is safe for general use?
Medsafe does not conduct studies. Medsafe reviews the data submitted by the pharmaceutical company, including clinical trial data. See above for more information on the types of data that is required.

WHAT ARE THE ACCEPTABLE NUMBER OF SIDE EFFECTS? We encourage healthcare professionals and consumers to report any suspected side effect to a COVID-19 vaccine. For this reason, and because so many people will be receiving a vaccine, we expect many side effects to be reported.
Receiving large numbers of reports also indicates that the reporting system is working and easy to use.

Research and Data on vaccinating young people. https://www.health.govt.nz/our-work/diseases-and-conditions/covid-19-novel-coronavirus/covid-19-vaccines/covid-19-vaccine-health-advice/covid-19-vaccine-and-children-information-parents-and-caregivers (US Wide- over 17 million 12-15yr ods in the US)

Immunization Advisory Centre. https://covid.immune.org.nz/faq/myocarditis-and-covid-19-vaccine-new-zealand
Myocarditis and the COVID-19 vaccine in New Zealand
An increased risk of heart inflammation (myocarditis, pericarditis, or both) has been observed in people who have received mRNA COVID-19 vaccines in overseas studies, particularly in males under 30 years of age after the second vaccine dose.
After treatment, many patients live long, full lives free from the effects of myocarditis. For others, however, ongoing cardiovascular medication or even a heart transplant may be needed

Covid-19: Vaccinations for children aged 5 to 11 due to begin …
https://www.stuff.co.nz › … · Whakamāoritia tēnei whārangi
1 Haki 2021 — Vaccinations for children aged 5 to 11 years are expected to start before the end of January reportef Covid-19 Response Minister Chris Hipkins PLEASE NOTE WHAT MEDSAFE REPORTS AS TO SAFETY FOR CHILDREN POST COVID JABS- Do not state Safe or Not. Do not respond to safety post jab question as a Yes or No.

Covid-19: Pfizer vaccine approved for children aged 5-11…
Medsafe has granted provisional approval for the Pfizer COVID-19 vaccine for children aged 5 to 11 years old.
Pfizer has plans to trial the vaccine in children aged 6 months to 5 years, and Moderna has ongoing trials to test the safety and efficacy of vaccines in children under 12 years old.
Pfizer revealed that there were very few serious adverse events and no deaths during the phase 2 and 3 trials of children aged 5–12 years. He also explained that the side effects were similar to those that adults experience

October 29, 2021 https://www.fda.gov/news-events/press-announcements/fda-authorizes-pfizer-biontech-covid-19-vaccine-emergency-use-children-5-through-11-years-age

WHAT IS EMERGENCY USE AUTHORIZATION ? An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives. Taking into consideration input from the FDA, manufacturers decide whether and when to submit an EUA request to FDA.
Once submitted, FDA will evaluate an EUA request and determine whether the relevant statutory criteria are met, taking into account the totality of the scientific evidence about the vaccine that is available to FDA.

https://www.medsafe.govt.nz/COVID-19/q-and-a-vaccine-approval.asp

INFORMATION FOR THOSE THAT SAY THE NUREMBERG TRIALS (NUREMBERG CODE) NO LONGER RELATE TO HUMAN RIGHTS VIOLATIONS TODAY:-

REFERENCES ARE MADE TO THE: United Nations A/64/272 General Assembly Distr.: General 10 August 2009
Sixty-fourth session Item 71 (b) of the provisional agenda

Promotion and protection of human rights: human rights questions, including alternative approaches for improving the effective enjoyment of human rights and fundamental freedoms

This report discusses the need for laws and international instruments to take into account the vulnerability of certain individuals whose rights are compromised owing to deeply rooted power imbalances and structural inequalities, presenting particular responsibilities to States and health-care providers to protect the human dignity and autonomy of all persons.
In the recommendations, the Special Rapporteur urges: –
(a) States to meet their obligations to safeguard informed consent through legislative, political and administrative mechanisms;
(b) Health-care providers to be cognizant that, according to their duty to act in the best interests of the patient, they are key players in protecting informed consent
(c) National and international bodies to emphasize the importance of informed consent as a fundamental aspect of the right to health in relevant policy and practice.

The concept of consent has evolved for centuries to arrive at its current meaning. In the aftermath of the Nuremberg Trials, increased international recognition of patients’ rights developed in the twentieth century, defining the responsibility of health-care providers and States responsibilities to the patient.

In 1947, the Nuremberg Code asserted that the voluntary consent of the human subject to medical research is necessary under all circumstances. The Declaration of Helsinki (1964) further developed the Code principles and tied them to the ethical duties of physicians, as outlined in the Declaration of Geneva (1948)

In 1994, the World Health Organization Amsterdam Declaration on Patients’ Rights required informed consent as a prerequisite for any medical intervention, guaranteeing also the right to refuse or halt medical interventions.
Informed consent is not mere acceptance of a medical intervention, but a voluntary and sufficiently informed decision, protecting the right of the patient to be involved in medical decision-making, and assigning associated duties and obligations to health-care providers. Its ethical and legal normative justifications stem from its promotion of patient autonomy, self-determination, bodily integrity and well-being. Important components of informed consent are discussed below-

Respect for legal capacity Competency to consent is a status known as legal capacity generally determined by the ability to comprehend, retain, believe and weigh information provided in arriving at a decision. Legal capacity is presumed in adult persons and renders them the right to consent to, refuse or choose an alternative medical intervention.