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  • The New Pharmaceutical Business Model

The New Pharmaceutical Business Model

gparkof1July 4, 2021July 17, 2021 Covid 19

  Here is the Pharmaceutical Business Model:

 

  •     Create a market for a new vaccine by causing a world-wide Pandemic.
  • Fund Gain of Function Research at U.S.  Bio- Safety-Labs . Transfer technology to China Via Wuhhan Institute,  Blame China for release of Covid-19 Virus
  •  Have government fund vaccine development and research. Then sell vaccines to Governments
  •      Government finances cost of vaccine development and purchase by adding to the trillion dollar deficit.
  •      Keep the playing field clear – Widespread use of Ivermectin or Hydroxychloroquine/Zine could knock out the demand for the vaccine. Withhold treatment from patients with  early stage Covid infection.
  •       Keep the VAERS mechanism for reporting adverse from the vaccines  dysfunctional. In Israel there is no reporting system for adverse effects.
  •        Censor reports of adverse effects on Social Media, Facebook and other media.
  •      Minimize the incidence of adverse effects.
  •        Increase the market by including children.  
  •       Ensure that Agency Capture is in place – that is the agencies designed to monitor the pharmaceuticals are captured by various techniques of musical chairs. High government officials look forward to the prospect of lucrative positions as top officials at the  CDC and NIH.
  •       Ensure the cooperation of presidents, heads of state, and heads of the dominant Health Authority via some financial or political incentive.
  • Most important of all, no liability for the Pharmaceuticals under any conditions.

Here is the law:

42 U.S. Code § 300aa–22 – Standards of responsibility

  • U.S. Code
  • Notes
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(a) General rule

Except as provided in subsections (b), (c), and (e) State law shall apply to a civil action brought for damages for a vaccine-related injury or death.

(b) Unavoidable adverse side effects; warnings

(1)

No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death associated with the administration of a vaccine after October 1, 1988, if the injury or death resulted from side effects that were unavoidable even though the vaccine was properly prepared and was accompanied by proper directions and warnings.

(2) For purposes of paragraph (1), a vaccine shall be presumed to be accompanied by proper directions and warnings if the vaccine manufacturer shows that it complied in all material respects with all requirements under the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 301 et seq.] and section 262 of this title (including regulations issued under such provisions) applicable to the vaccine and related to vaccine-related injury or death for which the civil action was brought unless the plaintiff shows—

(A)

that the manufacturer engaged in the conduct set forth in subparagraph (A) or (B) of section 300aa–23(d)(2) of this title, or

(B)

by clear and convincing evidence that the manufacturer failed to exercise due care notwithstanding its compliance with such Act and section (and regulations issued under such provisions).

(c) Direct warnings

No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death associated with the administration of a vaccine after October 1, 1988, solely due to the manufacturer’s failure to provide direct warnings to the injured party (or the injured party’s legal representative) of the potential dangers resulting from the administration of the vaccine manufactured by the manufacturer.

(d) Construction

The standards of responsibility prescribed by this section are not to be construed as authorizing a person who brought a civil action for damages against a vaccine manufacturer for a vaccine-related injury or death in which damages were denied or which was dismissed with prejudice to bring a new civil action against such manufacturer for such injury or death.

(e) Preemption

No State may establish or enforce a law which prohibits an individual from bringing a civil action against a vaccine manufacturer for damages for a vaccine-related injury or death if such civil action is not barred by this part.

(July 1, 1944, ch. 373, title XXI, § 2122, as added Pub. L. 99–660, title III, § 311(a), Nov. 14, 1986, 100 Stat. 3773; amended Pub. L. 100–203, title IV, § 4302(b)(1), Dec. 22, 1987, 101 Stat. 1330–221.)

 

 


—

Gerald Parkoff

gparkof1@gmail.com

 

https://hardball.parkoffletter.org
https://parkoffletter.org/
054-809-9503
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