This never happens since WW2.
Gen-Therapy are dangerous and produced by bad manufacturing practice. From 10 years to 10 months in the process and we give it pregnant woman and baby’s over 6 month old. This is never happens bevor.
Please protect your citizens!
Dear Mr Kalleli,
Thank you for your email of 4 April 2022 in which you provide us with your input on matters concerning the COVID-19 vaccines.
In your message, you argue that the COVID-19 vaccines authorised so far in the EU fall in your view under the definition of gene therapy medicinal products.
Please note that, as mentioned in Directive 2001/83/EC, Annex I, Part IV (as amended by Commission Directive 2009/120/EC):
Gene therapy medicinal product means a biological medicinal product which has the following characteristics:
(a) it contains an active substance which contains or consists of a recombinant nucleic acid used in or administered to human beings with a view to regulating, repairing, replacing, adding or deleting a genetic sequence;
(b) its therapeutic, prophylactic or diagnostic effect relates directly to the recombinant nucleic acid sequence it contains, or to the product of genetic expression of this sequence.
- Pause for input;
The American Society of Gene & Cell Therapy (ASGCT);
Definition of gene therapy is the introduction, removal or change in genetic material spesifically DNA or RNA into the cells of a patient to treat a specific disease. Becouse the Pfizer and Moderna Vaccines deliver mRNA in to cells, we consider them to fall under our definition of gene therapy.
- Back to the letter;
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Gene therapy medicinal products shall not include vaccines against infectious diseases.
- Pause;
Pay infinent attention to the following;
- The following companies think it is a Genetic Vaccine for infectious diseases;
- Hansonwade, Thermofisher, CureVac, AstraZeneca, Moderna, Pfizer, INOVIO, BioNTech, GSK
The letter continues;
Therefore, irrespectively of whether a vaccine against infectious diseases contains recombinant nucleic acids and regulates the expression of human genes, it does not fall under the definition of gene therapy under the EU legislation.
This definition was introduced in the EU legislation in 2009, well before the EU authorization of the Covid-19 vaccines.
- Pause;
This is what is known as;
Color of law simply means that a person in a government official capacity, who holds the authority to implement the law, commits an illegal action under the appearance of authority, which exceeds such authority.
Specifically, it is a violation of federal law for a lawful process to be perverted or used by a civil servant for an illicit purpose to intimidate, unduly burden, or harm another.
LINK:
https://www.lawinsider.com/dictionary/color-of-law
- The letter continues;
I would like to reassure you that all medicinal products authorised in the EU – including those categorized as gene therapy, vaccines, biologicals, or chemically-based medicinal products – undergo a strict quality, safety and efficacy assessment according to the high standards required by the EU legislation.
These high standards also apply to labeling and classification of pharmaceutical products.
- Pause for Information from the letter from Mr Adam Griffiths at Hansonwade;
Adam writes;
Dear Kjell Tore
I’m currently researching on Genetic Vaccines Advanced Analytical tools, namely comprehensive methods to assess plasmid purity, viral vector evaluation, and assays for mRNA.
Regardless of vaccine technology, it is essential to confirm that a desired antigen is expressed and that adequate T-cell responses are achieved, ensuring that novel quality vaccines are continued to be brought to market after COVID-19, not just for infectious diseases, but also for other high interest areas such as cancer and rare diseases.
This new summit planned for early 2021 in a physical format will focus on the analytical development of mRNA, DNA, and viral vector-based vaccines, and will be the sister summit of the recent Genetic Vaccine Development for Infectious Diseases Summit, which took place in May this year:
https://genetic-vaccine-development.com/
Adam Griffiths M.Sc
Senior Program Manager, Vaccines
Hanson Wade
–
- The letter continues;
A marketing authorisation is granted to a medicinal product in the EU only after its quality, safety and efficacy have been thoroughly evaluated and a positive benefit-risk balance related to its use has been concluded.
- Pause for input from the Genetic Vaccine Summit;
From initiation of clinical development in March 2020 to initial authorizations in December 2020.
While conducting Phase 1, Phase 2, and Phase 3 studies safely and in parallel.
(Input: Meaning we ran all the trails at the same time)
- Facts from the world’s first RNA drug Onpattro:
Fun fact; Onpattro uses the same Lipid Nano Particle technology (MC3) as the Pfizer/BionTech Genetic Vaccine for Covid-19.
Input from the safety package insert of the world’s first RNA drug Onpattro;
- You should not use Onpattro if you are pregnant unless your doctor advises. If you are of childbearing age and intend to use Onpattro, you should practice effective contraception.
- Breast-feeding Ingredients of Onpattro may pass into breast milk. Talk to your doctor about stopping breastfeeding or treatment with Onpattro.
- Children and adolescents Onpattro is not recommended in children and adolescents under 18 years of age.
From the Norwegian Medicine Agency
Patisiran (Onpattro)
Type of method: Drug; Gene therapy
Area: Neurology
Active substance: Patisiran
(Input; You see Onpattro is not a genetic vaccine against infectious diseases so therefore it is a Gene Therapy Product.)
As just stated by EMA;
Gene therapy medicinal products shall not include vaccines against infectious diseases.
Last note regarding Onpattro;
- while it is an approved drug, it’s still classified as an investigational drug.
- The same classification also holds true for all the Genetic Vaccines for Covid-19.
The FDA Definition of an investigational drug is:
- A substance that has been tested in the laboratory and has been approved by the U.S. Food and Drug Administration (FDA) for testing in people. Clinical trials test how well investigational new drugs work and whether they are safe to use.
____________________________________________________________________________
- The letter continues;
–
Furthermore, pharmaceutical products that have been granted a marketing authorisation by the European Commission are under constant monitoring by national competent authorities and by the European Medicines Agency (EMA), under an efficient Pharmacovigilance system, which ensures timely detection of any potential risk and swift appropriate action.
The EMA webpage ‘COVID-19 Vaccines: Authorised’2 is regularly updated and contains detailed safety updates for each COVID-19 vaccine authorised in the EU.
I would like to reassure you that the European Commission and the EMA are fully committed to ensure the highest protection of the health of EU individuals.
Yours sincerely,
Olga Solomon
Head of Unit
____________________________________________________________________________
Link to letter;
https://drive.google.com/file/d/1KpKiuXdzfc4Td6qi-PT_PQVHwJGmAJsT/view?usp=drivesdk
Highlighted;
https://drive.google.com/file/d/1TMU0hCkCnF_JW9jmu7Owv-dWb6cIgSih/view?usp=drivesdk
1 https://vaccination-info.eu/en/vaccine-facts/monitoring-vaccine-safety-and-reporting-side-effects
- END OF EMA LETTER
____________________________________________________________________________
Here is the safety data they don’t tell you about unless you look for yourself;
July 30, 2022
Source:
https://www.adrreports.eu/en/index.html
For more details see my substack Genetic Vaccine Damage Report;
https://drive.google.com/uc?id=135YFSSfN-yVhgNZHZnBCbmC03rdItyvX&export=download
The shots are dangerous because they are bad manufacturing practice. From 10 years to 10 months in the process and we give it pregnant woman and baby’s over 6 month old this is never happens bevor. This is crime against humanity
Former ethics researcher at the W.H.O, Astrid Stuckelburger, PhD, sheds light on how our top world health agencies have used the COVID-19 pandemic to push a dangerous global agenda.
https://thehighwire.com/ark-videos/w-h-o-whistleblower-exposes-onehealth-agenda/
Covid 19 researcher blow the whistle on Pfizer’s data integrity in the Trials https://www.bmj.com/content/375/bmj.n2635
ACTIVATE NUREMBERG 2.0!
Mr. Alex Azar, DEFENDANT
Dr. Anthony Fauci, DEFENDANT
Dr. Peter Daszak, DEFENDANT
Dr. Ralph Baric, DEFENDANT
FDA, DEFENDANT
CDC, DEFENDANT
NIAID, DEFENDANT
MODERNA, DEFENDANT
PFIZER, DEFENDANT
–
Count 1: 18 U.S.C. § 2331 §§ 802 – Acts of Domestic Terrorism resulting in death of American Citizens
Count 2: 18 USC $ 2339- Conspiring to Commit Acts of Terrorism
Count 3. 15 U.S.C. $1-3 – Conspiring to criminal commercial activity
Count 4. 18 USC $ 175 – Funding and Creating a Biological Weapon
Count 5. 15 U.S.C. §8 – Market manipulation and allocation
Count 6. 18 U.S.C. § 1001 – Lying to Congress
Count 7. 15 U.S.C. § 19 – Interlocking directorates
Count 8. 18 U.S. Code § 2384 – Seditious conspiracy
–
Supreme Court Action
https://youtu.be/8s3EUksu2Fw
–
Attorney General Document
https://www.fullyliveacademy.com/attorneygeneraldocument
–
GATES, FAUCI, AND DASZAK CHARGED WITH GENOCIDE IN INTERNATIONAL COURT FILING t.me/drue86/12500
https://www.fullyliveacademy.com/attorneygeneraldocument
Make Ivermectin, Budesonide, & Hydroxychloroquine available over-the-counter.
All but one patient (99.6%; n = 236/237) treated with HCQ, AZM, and zinc with or without high-dose IV vitamin C (IVC) fully recovered. – https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC8712288/
Budesonide (Common FDA Approved Asthma Treatment Reduces Need for Hospitalisation for COVID-19) – https://www.ox.ac.uk/news/2021-02-09-common-asthma-treatment-reduces-need-hospitalisation-covid-19-patients-study
“If you take ivermectin for COVID-19 you will not get sick.” | 100% Effective COVID-19 Treatments – https://www.bitchute.com/video/OzrAVkI3nLIf/
• Front Line COVID-19 Critical Care Alliance | MATH+ and I-MASK+ protocols (source of the bitchute Ivermectin video linked above https://covid19criticalcare.com/
• FLCCC Alliance Response to the NIH Guideline Committee Recommendation on Ivermectin use in COVID-19 dated January 14th, 2021
Deutschland finanziert Gates-Projekte mit 3,8 Milliarden Euro
Social prosthetic theory
This is crime against humanity!
JULIMINATION 
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