RE: “COVID-19: 08/10/2021 Vaccine Protocol Pfizer Comirnaty® that is “legally distinct” with “certain differences” from the 20/08/2021 DoH Vaccine Protocol Pfizer BNT162b2 EUA & unlicensed vaccine

……………………….NOTICE-FOR-FREEDOM-OF-INFORMATION-ACT-2000
………………………………..FOR-THE-PUBLIC-RECORD
.….……………….…………………………………………………Mary Anne: McCloskey:
………...……..…………………………acting in her capacity as ‘Dr Anne McCloskey’
.…............................................………………………………………20 September 2023

michael oliver: mcbride: a living man
doing business as (dba) MICHAEL OLIVER MCBRIDE
acting as Chief Medical Officer
acting in the capacity of ‘Dr. Michael McBride (GMC 3205114)’
DEPARTMENT-OF-HEALTH
Castle Buildings, Stormont, Belfast

peter: may: a living man
doing business as (dba) PETER MAY
acting as Permanent Secretary Department of Health and
Chief Executive of Health and Social Care
DEPARTMENT-OF-HEALTH
Castle Buildings, Stormont, Belfast

Notice to the Principal is Notice to the Agent; Notice to the Agent is Notice to the Principal

RE: “COVID-19: 08/10/2021 Vaccine Protocol Pfizer Comirnaty® that is “legally distinct” with “certain differences” from the 20/08/2021 DoH Vaccine Protocol Pfizer BNT162b2 EUA & unlicensed vaccine "

Greetings Dr. Michael Oliver McBride (GMC 3205114) and Peter May

WHEREAS On Friday 20 AUGUST 2021 the DEPARMENT-OF-HEALTH’s issued a 30 page Vaccine Protocol for the UNLICENSED VACCINE under, Emergency Use Authorisation (temporary authorisation) Regulation 174 of the Human Medicines Regulation 2012 as amended: “COVID-19 mRNA Vaccine BNT162b2 (Pfizer/BioNTech Vaccine)” that was issued and valid from and signed 20/08/2021 by Robin Swann MLA, Minister of Health; Dr Michael McBride, Chief Medical Officer; Professor Charlotte McArdle, Chief Nursing Officer; Cathy Harrison, Chief Pharmaceutical Officer and on page 12 it states “Children and young people have a very low risk of COVID-19, severe disease or death due to SARS CoV-2 compared to adults… The Pfizer BioNTech [BNT162b2] vaccine has approval for use from 12 years of age…”.

From page 14 of 30 of this protocol: “Black triangle COVID-19 mRNA BNT162b2 vaccine did not have a UK marketing authorisation [unlicensed] at the time this protocol was written and is authorised for temporary supply in the UK in accordance with a Regulation 174 authorisation [Human Medicines Regulation 2012 as amended].

As a new vaccine product, MHRA have a specific interest in the reporting of adverse drug reactions for this product, see https://yellowcard.mhra.gov.uk/the-yello... ”

From page 10 of 30 of this protocol: “Myocarditis and pericarditis There have been very rare reports of myocarditis and pericarditis occurring after vaccination with COVID-19 mRNA Vaccine BNT162b2 [Pfizer / BioNTech] often in younger men and shortly after the second dose of the vaccine.”

‘FOI DOH 2023 0197 COVID-19: 20/08/2021 DoH Vaccine Protocol Pfizer BNT162b2 re children injected with an unlicensed vaccine under EUA Regulation 174 & signed by Dr Michael McBride, CMO’
https://www.whatdotheyknow.com/request/c...

WHEREAS On Saturday 21st August 2021, as part of lawful whistleblowing I made a 10 minute public interest disclosure in accordance with The Public Interest Disclosure Order 1998, the GMC’s Good Medical Practice and the GMC’s Guidance, ‘Raising and acting on concerns about patient safety’
https://www.gmc-uk.org/-/media/documents... and the GMC’s guidance on Informed Consent ‘Guidance on professional standards and ethics for doctors Decision making and consent’ https://www.gmc-uk.org/-/media/documents... included this statement regarding COVID-19 mRNA vaccination BNT162b2 Pfizer BioNTech:

“These injections are doing real harm. They are certainly not providing any visible protection for people and they are still in clinical trials for another two years. They are unlicensed and unapproved. The have emergency [use] authorisation on the premise of the false assumption that there are no other treatments available for Covid“ …

WHEREAS on the 26 April 2023 DEPARTMENT-OF-HEALTH’s DOH/2023-0092 Freedom of Information supply to me for ‘COVID-19 Dr. Michael McBride, Chief Medical Officer’s email on Saturday 21 August 2021 at 23:15 (11:15pm) re: “The Irish Inquiry – A message from Dr. Anne McCloskey | Facebook" https://www.whatdotheyknow.com/request/c...

WHEREAS over 20,000 members of the public have signed a change.org petition to reinstate ‘Dr McCloskey’ https://www.change.org/p/hscb-re-instate...

WHEREAS from the 9 May 2023 over 18,000 members of the public have viewed and read Citizen Journalists “How the corporate media [ @irish_news & @BelTel ] pressured the Health Board into suspending a doctor. This is a story of how corporate media interfered with due process to pressure the Department of Health and the Health and Social Care Board into censoring and suspending a doctor for saying things they didn’t like” https://citizenjournos.com/2023/05/08/ho...

WEREAS Pfizer-BioNTech COVID-19 mRNA vaccine BNT162b2 batches / stock / product was unlicensed and under Emergency Use Authorisation from 02 December 2020 by the UK Licensing Authority through Regulation 174 of the Human Medicines Regulations 2012 “with all remaining Regulation 174 stocks expiring at the end of February 2022” according to public servants at the Department of Health through FOI DOH/2023- 0136 issued 13 June 2023.

WHEREAS on 23 August 2021, the Food and Drug Administration (FDA) of the United States did the following:

a) 23 August 2021 - in a letter the FDA reissued the Emergency Use Authorisation (EUA) for Pfizer-BioNTech COVID-19 mRNA vaccine BNT162b2.

b) 23 August 2021 – in a separate letter the FDA issued its approval of the Biologics license application [for the UK / EU see (conditional) Marketing Authorisation] for Pfizer-BioNTech COVID-19 mRNA vaccine Comirnaty®.

c) 23 August 2021 – FDA stated in writing that "there is not sufficient approved vaccine [Pfizer-BioNTech COVID-19 mRNA vaccine Comirnaty®] available for distribution" in the U.S.

d) 23 August 2021 – The FDA stated in writing that Pfizer - BioNTech COVID-19 vaccine Comirnaty® and Pfizer-BioNTech COVID-19 vaccine BNT162b2 were

i) "legally distinct" with

ii) "certain differences"

e) 23 August 2021 U.S. Senator Ron Johnson’s wrote to the FDA “together with the fact that the FDA issued two [2] distinct letters – one extending the EUA for the [Pfizer-BioNTech COVID-19 vaccine BNT162b2] vaccine used in the U.S. and the other granting the FDA approval of the Comirnaty [Pfizer - BioNTech COVID-19 vaccine Comirnaty®] vaccine used in Europe and other countries – has caused a great deal of confusion.”

See https://www.ronjohnson.senate.gov/servic... and https://www.ronjohnson.senate.gov/2021/1...

WHEREAS the Western Health and Social Care Trust state that Pfizer-BioNTech COVID-19 mRNA vaccine Comirnaty® “(i.e. licensed Pfizer vaccine) was supplied for use to the Mass Vaccination Centre (MVC / Foyle Arena [Londonderry]) on 10th September 2021.” Western Health and Social Care Trust FOI/23/1015 dated 26th June 2023.

WHEREAS this verifies that on Saturday 21 August 2021 in the Western Health and Social Care Trust mass vaccination centre – the unlicensed and under Emergency Use Authorisation through Regulation 174 of the Human Medicines Regulations 2012 Pfizer - BioNTech COVID-19 mRNA vaccine BNT162b2 batches / stock / product - were deployed and being used per my whistleblowing public interest disclosure / protected disclosure made and uploaded on Saturday 21 August 2021.
THEREFORE in accordance to the Freedom of Information Act 2000 you both are hereby required to supply and provide the following:

1. The full and complete ‘v02.00 “Vaccination protocol for Comirnaty® COVID-19 mRNA Vaccine (Pfizer/BioNTech Vaccine)” valid from: 8 October 2021 and with the DEPARTMENT-OF-HEALTH logo on page 1 of 32 and states “The Health and Social Care Board and Public Health Agency have developed this protocol for authorisation by the Minister of Health to facilitate the delivery of the national COVID-19 vaccination programme in Northern Ireland" and Ministerial Authorisation signed by Robin Swann MLA, “Minister for Health”; Clinical Authorisation signed by Dr David Irwin, “Consultant in Health Protection PHA [PUBLIC HEALTH AGENCY]”; Deirdre Webb, “Assistant Director for Public Health Nursing for Children and Young People PHA [PUBLIC HEALTH AGENCY]”; Joe Brogan, “Assistant Director Integrated Care, HSCB [HEALTH AND SOCIAL CARE BOARD]” and on page 15 and 16 of 32 it states: “Identification & management of adverse reactions” and lists a number of adverse reactions including, but not limited to, “arthralgia and pyrexia”, “myalgia”, “Lymphadenopathy”, “Myocarditis and pericarditis”, “Guillain-Barre Syndrome”, “anaphylaxis”.

As you are aware as a public servant it is your duty “to confirm or deny” in accordance to the Freedom of Information Act 2000 Part I ‘Right to Information’ Section I.

I do not consent to redactions for the names and job titles of public servants including, but not limited to, employees, agents, assistant directors, employment liaison adviser (ela), communication directors, deputy chief medical officers of the DEPARTMENT-OF-HEALTH, the HSCNI, the HEALTH-AND-SOCIAL-CARE-BOARD, GENERAL-MEDICAL-COUNCIL Northern Ireland Executive, MLA s, MP’s, members of the House of Lords, politicians and/or regulatory bodies as these are all public servants.

As you both are aware, a public servant holds a public office and operates in the public in order to serve and protect the public, and is NOT a private servant, thus a public servant’s name and job title must NOT be redacted.

The information requested is of public interest and concerns the health and safety of the public. The DEPARTMENT-OF-HEALTH exists for one purpose only - to give services to the public and has no other purpose. This is not a gift or an altruistic service - it is a public service paid for with public money.

I have the reasonable expectation that you, michael oliver: mcbride: a living man, acting as a public servant in the public office of Chief Medical Officer and in the capacity as ‘Dr Michael McBride (GMC 3205114)’ for the DEPARTMENT-OF-HEALTH, will honour and adhere to, your position of trust, the Seven Principles of Public Life, your duty of care, duty of candour, common law obligations, statutory obligations and protocols that govern public servants.

I have the reasonable expectation that you, peter: may: a living man, acting as a public servant in the public offices Permanent Secretary Department of Health and Chief Executive of Health and Social Care for the DEPARTMENT-OF-HEALTH, will honour and adhere to, your position of trust, the Seven Principles of Public Life, your duty of care, duty of candour, common law obligations, statutory obligations and protocols that govern public servants.

The 7 principles of public life are: Honesty; Openness; Leadership; Integrity; Accountability; Objectivity and Selflessness.
https://www.gov.uk/government/publicatio...

This notice will be used as evidence.

I require that there is a complete response to this FOI request on DEPARTMENT-OF-HEALTH official letter-headed paper, wet ink signed and dated.

This notice is sent without ill will, without vexation, and without frivolity. You are also hereby noticed that it is not my intention to harass, intimidate, offend, conspire, blackmail, coerce or cause anxiety, alarm or distress, as this notice is part of due process.

You have been noticed. Govern yourself accordingly.

…………………………………………...With honour and in pure truth,

………………………..………….…………………………...By: mary anne: mccloskey:
……......……………………………………………………………….All rights Reserved:
...…….……………………………………………………………All Freedoms Reserved:
….……………………………….............Acting in the capacity of Dr Anne McCloskey:
........…………….Settlor, Executor and Beneficiary for any and all derivatives of / for
….……...……………………………………………………MARY ANNE MCCLOSKEY:
……...………………………………………………...Without recourse Non-Assumpsit:

cc To all whom it may concern.