The Pfizer testimony by Melissa Mac Atee

Pfizer Testimony by Melissa Mac Atee

1. Melissa McAtee
Pfizer Testimony
Employed by Kelly Services to be a temp for Hospira in September 2012
First job was a Pharmaceutical Assistant for P6
Converted to full time Hospira Employee April 2013
Pfizer Purchased Hospira in 2015
Promoted to Manufacturing Quality Auditor in April 2017
Went on a Mental Health LOA August 24, 2021
Project Veritas Interview aired October 6, 2021
Terminated by Pfizer October 20, 2021

3. My Maiden name is
Strickler
•I was Married July 3, 2021
•Pfizer had not given me a new badge by the time I left.

5. Why | am speaking out

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strengthened aid pain and Congress expected th mos quí um ass wou vee defense
trace fod 10 the las decae. he majority ol eases have metad hoc apa the ha ete
Even no cua questions wil be rand inci (1) Even with the
lam “ascot submited? (2) Had the FDA known aout the ala wea han
re rom any fre Petew et GU What aout the abe fever sistem made he

Congress stated the rationale for imposing cGMP on the pharmaceutical industry
this way

‘The manufacturing of drug is a busines that require
“and special laboratory and other (cities and most careful internal manu.

ing poca ad cing costo These top a may te
Pr re a wl a 0 far as posible
in the deny APE qua erty nt A al they por a

‘The purpose of the cGMP requirement isto prevent injury and death “by building
quality into the design and production of pharmaccutials,”* so that substandard

‘equipped manufacturing
s. adequately trained personnel, precisely controlled manufacturing pro-
cesses appropriate laboratory controls, complete and accurate records and reports,
appropriate finished product examination, and so on. Current GMPS are not “best
practices" rather, they establish threshold OMNIA Standards which must be
ied in order for a pharmaceutical manufacturing operation to be compliant

is in the same position as any other contractor which is required
19 conform to contractual or regulatory standards The basis of liability under the

because the payor (in this case. the United States) is potentially PIRE SUBS.
dater covered up by false statements

documents required to be completed under the cGMP

It makes sense, too: The CGMP are a set of regulations which, by their very
nature, are designed to ensure that drugs are manufactured in such a way that they
‘meet the requirements of the federal Food, Drug and Cosmetic Act as 10 safety and
have the identity and strength and meet the purty characteristics that they purport
or are represented to possess. The major federally funded government health care
programs, Medicare and Medicaid, operate under the express provisions that they

will only pay for medical services and products that are “reasonable and necessary”

D corde

ingly as the theory goes, the United States suffers moneta
TD

federally funded health care programs spend billions of dollars every year on
pharmaceuticals

False representations conce
bass for FCA lability

ing minor or technical violations will not be the

e
The common thread through
‘each violation is thatthe violation is severe enough so that Ihe drug product that

8. The Glowing Vials

13. Black light No light
Regular Flashlight

21. The Emails

From: Badkar, Advalt V <advat.v [email protected]>
Sent: Thursday, February 4, 2021 1:26 PM

To: Dormitzer, Pip Ralph «Philp. Dormitzer@pfizer. com>; Swanson, Kena Anne

kena [email protected]>

‘Subject: FW: Medical Information enquiry regarding COVID-19 mANA Vaccine BNT16262

Hithere,
assume the answer to the question In “bol” below is NO. Can you confirm?

Thanks,
Aat

mageoo7 pne>

From: Qureshi, Ambereen <[email protected]>
Sent: Wednesday, February 3, 2021 8:11 AM

To: Weiser, Sarah Elizabeth «Sarah Welzer@pfzercom>

Ce: Barras Ana <[email protected]>

Subject: Medical Information enquiry regarding COVIO-19 mRNA Vaccine BNT16262

Dear sarah,

"hope that you ae well
have received an enquly as follows:

“did Pfizer make use of cell line from an aborted foetus when carrying out any confirmatory tests for
this vaccine?”

We have already confirmed with the customer that no 001 ines from an aborted foetus were used in the
manufacturing process of the COVID-19 mRNA Vaccine BNT16262.
Do we have any information to provide in response to her question?

30. The Graphene Oxide Emails

From: Van zylsandra <[email protected]>
Sent: Monday, July 12, 2021 6:11 AM

To: Hays, Steven <[email protected]>

(Ce: Weiser, Sarah Elizabeth <[email protected]>
Subject: RE:

Good morning Steve
Trust you had a lovely weekend and doing well!

1 just wanted to check If below statement is acceptable regarding Graphe Ble, please? see that Sarah is 000.
Wereceived qute few enquires onthis @ 0

pp ey me pr ct

We cannot guarantee that minute amounts of substances ore not contained in raw materials obtained from our
suppliers. To ensure we have a consistent and reliable supply of medications, we must use a network of suppliers and
manufacturing sites globally for both active and inactive ingredients

| appreciate your help!

Kind regards
Sandra

60. •This is a sworn testimony. I swear all claims are true due to my
experience
•All evidence is not presented due to lack of understanding scientific
lingo

For interviews and government officials
[email protected]