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SCHEDULES

Regulation 3A(2)

[F1SCHEDULE 2BN.I.Criteria to be [F2an eligible] arrival

1.  P is [F3an “eligible”] arrival if P complies with any of paragraphs 2 to 6.N.I.

2.  P complies with this paragraph if P—N.I.

(a)has completed a course of doses of an authorised vaccine with the final dose having been received before the start of the period beginning with the 14th day before the date of P’s arrival in Northern Ireland,

(b)received that course of doses in the United Kingdom or a relevant country,

(c)if the course of doses was received in the United States of America, is ordinarily resident in the United States of America,

(d)is able to provide proof, if required by an immigration officer or the operator of the relevant service on which P travels to Northern Ireland, of meeting the requirement in sub-paragraph (a) through—

(i)the NHS COVID pass, certification issued by the Department of Health, or equivalent from NHS Scotland or NHS Wales,

(ii)the EU Digital COVID Certificate, F4...

(iii)the Centres for Disease Control and Prevention vaccination card, [F5or]

[F6(iv)a vaccine certificate,]

(e)is able to provide proof, if required by an immigration officer or the operator of the relevant service on which P travels to Northern Ireland, of meeting the requirement in sub-paragraph (c), and

(f)has declared on the Passenger Locator Form that P meets the COVID-19 vaccination eligibility criteria F7....

3.  P complies with this paragraph if P—N.I.

(a)has participated, or is participating, in a clinical trial of a vaccine for vaccination against coronavirus carried out in accordance with the requirements of the Medicines for Human Use (Clinical Trials) Regulations 2004,

(b)is able to provide proof of such participation, if required by an immigration officer or the operator of the relevant service on which P travels to Northern Ireland, and

(c)has declared on the Passenger Locator Form that P meets the COVID-19 vaccination eligibility criteria F8....

4.  P complies with this paragraph if P—N.I.

(a)has participated, or is participating, in a clinical trial regulated in the United States of America by the Food and Drugs Administration of a vaccine for vaccination against coronavirus,

(b)is able, if required by an immigration officer or the operator of the relevant service on which P travels to Northern Ireland, to provide proof of such participation through the Centres for Disease Control and Prevention vaccination card,

(c)has declared on the Passenger Locator Form that P meets the COVID-19 vaccination eligibility criteria F9..., and

(d)is ordinarily resident in the United States of America and is able to provide proof of that residence, if required by an immigration officer or the operator of the relevant service on which P travels to Northern Ireland.

5.  P complies with this paragraph if P is—N.I.

(a)under the age of 18 years upon arrival in Northern Ireland, and

(b)ordinarily resident in the United Kingdom or a relevant country.

6.  P complies with this paragraph if P is either—N.I.

(a)a person who—

(i)has completed a course of doses of a vaccine under the United Kingdom vaccine roll-out overseas, with the final dose having been received before the start of the period beginning with the 14th day before the date of their arrival in Northern Ireland,

(ii)is able to provide proof, if required by an immigration officer or the operator of the relevant service on which P travels to Northern Ireland, of meeting the requirements in paragraph (i), and

(iii)has declared on the Passenger Locator Form that P meets the COVID-19 vaccination eligibility criteria F10..., or

(b)a dependent of a person of the description in any of paragraphs (a) to (c) of the definition of “United Kingdom vaccine roll-out overseas” and is under the age of 18 years upon arrival in Northern Ireland.

[F117.(1) For the purposes of paragraph 2—N.I.

(a)P has completed a course of doses if P has received the complete course of doses specified—

(i)in the summary of product characteristics approved as part of the marketing authorisation for the authorised vaccine, or

(ii)in the instructions for usage approved as part of the authorisation by the licensing authority on a temporary basis under regulation 174 (supply in response to spread of pathogenic agents etc) of the Human Medicines Regulations 2012 for the authorised vaccine;

(b)if P has received a dose of one authorised vaccine and a dose of a different authorised vaccine, P is deemed to have completed a course of doses of an authorised vaccine.]

F127A.  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .N.I.

[F137B.(1) For the purposes of paragraph 6—N.I.

(a)P has completed a course of doses of a vaccine if P has received the complete course of doses of the vaccine as specified in the manufacturer’s guidance for that vaccine;

(b)where P has received a dose of an authorised vaccine in the United Kingdom and a dose of a vaccine under the United Kingdom vaccine roll-out overseas, P is deemed to have completed a course of doses of a vaccine under the United Kingdom vaccine roll-out overseas;

(c)where P has received a dose of one vaccine under the United Kingdom vaccine roll-out overseas, and a dose of a different vaccine under the United Kingdom vaccine roll-out overseas, P is deemed to have completed a course of doses of a vaccine under the United Kingdom vaccine roll-out overseas.]

F148.  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .N.I.

F158A.  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .N.I.

9.  For the purposes of this Schedule a child is to be treated as making a declaration on a Passenger Locator Form, and providing any proof required, if that declaration is made, and the proof provided, by a person who is travelling with and has responsibility for that child.N.I.

10.  In this Schedule—N.I.

“authorised vaccine” means a medicinal product for vaccination against coronavirus [F16which—]

(a)

in relation to doses received in the United Kingdom [F17, is authorised]

(i)

for supply in the United Kingdom in accordance with a marketing authorisation, or

(ii)

by the licensing authority on a temporary basis under regulation 174 of the Human Medicines Regulations 2012;

(b)

[F18in relation to doses received in a relevant country listed in the table in paragraph 11, is authorised for supply in that relevant country following evaluation by the regulator for that relevant country,

(c)

in relation to doses received in a relevant country listed in paragraph 12, would be authorised as described in paragraph (a)(i) or (ii) if the doses were received in the United Kingdom,]

“clinical trial” has the meaning given in regulation 2(1) of the Medicines for Human Use (Clinical Trials) Regulations 2004,

[F19“the COVID-19 vaccination eligibility criteria” means the conditions in any of paragraphs 2 to 6,]

“Crown servant” has the meaning given in section 12(1)(a) to (e) of the Official Secrets Act 1989,

“government contractor” has the meaning given in section 12(2) of the Official Secrets Act 1989,

“the licensing authority” has the meaning given in regulation 6(2) (the licensing authority and the Ministers) of the Human Medicines Regulations 2012,

“marketing authorisation”—

(a)

in relation to a vaccine authorised for supply in the United Kingdom or in a member State, has the meaning given in regulation 8(1) (general interpretation) of the Human Medicines Regulations 2012,

(b)

in relation to a vaccine authorised for supply in a relevant country [F20listed in the table in paragraph 11] other than a member State, means a marketing authorisation granted by [F21the regulator for that relevant country],

“medicinal product” has the meaning given in regulation 2 (medicinal products) of the Human Medicines Regulations 2012,

“NHS COVID pass” means the COVID-19 records on the NHS smartphone app developed and operated by the Secretary of State, through the website at NHS.uk or a COVID-19 post vaccination letter obtained from the NHS,

“NHS” means the health service continued under section 1(1) of the National Health Service Act 2006,

“NHS Scotland” means the health service continued under section 1(1) of the National Health Service (Scotland) Act 1978,

“NHS Wales” means the health service continued under section 1(1) of the National Health Service (Wales) Act 2006,

[F22“regulator”, in relation to a relevant country listed in the table in paragraph 11, means the regulator identified in the corresponding row of the second column of the table in that paragraph, and a reference to a regulator in that table is a reference to the regulatory authority of that name designated as a Stringent Regulatory Authority by the World Health Organization pursuant to the operation of the COVAX Facility,]

“relevant country” means a country listed in the first column of the table in paragraph 11 [F23or a country or territory listed in paragraph 12],

F24...

“relevant service” means a commercial transport service carrying passengers to Northern Ireland from outside the common travel area,

“United Kingdom vaccine roll-out overseas” means the administration of vaccination against coronavirus to—

(a)

Crown servants, government contractors or other personnel posted or based overseas and their dependants under the scheme known as the Foreign, Commonwealth and Development Office staff COVID-19 vaccination programme;

(b)

residents of the British overseas territories, the Channel Islands and the Isle of Man, as part of a programme agreed in the overseas territory, any of the Channel Islands, or the Isle of Man with the United Kingdom government; or

(c)

military or civilian personnel, government contractors and their dependants at a military posting overseas, including the British overseas territories, the Channel Islands and the Isle of Man, under the vaccination scheme provided or approved by the UK Defence Medical Services.

[F25“vaccine certificate” means a certificate in English, French or Spanish issued by the competent health authority of a relevant country [F26, other than a European country listed in the table in paragraph 11 or the United States of America,] which contains—

(a)

P’s full name;

(b)

P’s date of birth;

(c)

the name and manufacturer of the vaccine that P received;

(d)

the date that P received each dose of the vaccine;

(e)

details of either the identity of the issuer of the certificate or the country of vaccination, or both.]

Textual Amendments

11.  The table referred to in [F27paragraph 10] follows—N.I.

Relevant countryRelevant regulator
a member StateEuropean Medicines Agency
AndorraEuropean Medicines Agency
[F28Australia The Therapeutic Goods Administration]
[F28CanadaHealth Canada]
IcelandEuropean Medicines Agency
LichtensteinEuropean Medicines Agency
MonacoEuropean Medicines Agency
NorwayEuropean Medicines Agency
San MarinoEuropean Medicines Agency
SwitzerlandSwissmedic
the United States of AmericaUnited States Food and Drug Administration
Vatican City StateEuropean Medicines Agency

[F2912.  The countries and territories referred to in the definitions of “authorised vaccine” and “relevant country” [F30in paragraph 10] are—N.I.

[F31Albania]

Antigua and Barbuda

[F31Bahamas]

Bahrain

[F31Bangladesh]

Barbados

[F31Bosnia and Herzegovina]

[F31Brazil]

Brunei

[F31Chile]

[F31Colombia]

Dominica

[F31Egypt]

[F31Georgia]

[F31Ghana]

[F31Grenada]

[F31Hong Kong]

[F31India]

[F31Indonesia]

Israel

[F31Jamaica]

Japan

[F31Jordan]

[F31Kenya]

[F31Kosovo]

Kuwait

Malaysia

[F31Maldives]

[F31Moldova]

[F31Montenegro]

[F31Morocco]

[F31Namibia]

New Zealand

[F31Nigeria]

[F31North Macedonia]

[F31Oman]

[F31Pakistan]

[F31the Philippines]

Qatar

Saudi Arabia

[F31Serbia]

Singapore

[F31South Africa]

South Korea

[F31St Kitts and Nevis]

[F31St Lucia]

[F31St Vincent and the Grenadines]

Taiwan

[F31Thailand]

[F31Turkey]

[F31Ukraine]

United Arab Emirates

[F31Vietnam]]

[F3213.(1) In the definition of “authorised vaccine” in paragraph 10, the reference to doses received in a relevant country listed in paragraph 12 includes doses administered to a person, otherwise than in a relevant country, by a person acting on behalf of the United Nations and authorised to administer the vaccination in that capacity.N.I.

(2) Where a course of doses of an authorised vaccine has been administered to a person, otherwise than in a relevant country, by a person acting on behalf of the United Nations and authorised to administer the vaccination in that capacity—

(a)the person to whom the doses have been administered is to be treated for the purposes of paragraph 2 as having received those doses in a relevant country listed in paragraph 12, and

(b)the reference in the definition of “vaccine certificate” in paragraph 10 to the competent health authority of a relevant country is to be construed as including the person acting on behalf of the United Nations.]]