National Health Security Regulations 2018

Part 1—Preliminary

1 Name

This instrument is the National Health Security Regulations 2018.

3 Authority

This instrument is made under the National Health Security Act 2007.

5 Definitions

Note: A number of expressions used in this instrument are defined in the Act, including the following:

(a) entity;

(b) facility;

(d) registered entity;

(e) security‑sensitive biological agent;

(f) SSBA;

(g) SSBA Standards.

In this instrument:

ABN has the same meaning as in the A New Tax System (Australian Business Number) Act 1999.

Note: ABN is short for Australian Business Number.

ACN has the same meaning as in the Corporations Act 2001.

Note: ACN is short for Australian Company Number.

Act means the National Health Security Act 2007.

affected: the body of a person or animal is affected by a security‑sensitive biological agent if the security‑sensitive biological agent has been introduced into the body.

ARBN has the same meaning as in the Corporations Act 2001.

Note: ARBN is short for Australian Registered Body Number.

Deputy Responsible Officer has the same meaning as in the SSBA Standards.

Geocentric Datum of Australia 1994 means the Geocentric Datum of Australia as defined in Gazette No. GN 35 of 6 September 1995, as existing when this instrument commences.

law enforcement agency has the meaning given by subsection 9(2).

Responsible Officer has the same meaning as in the SSBA Standards.

sensitive information, in relation to a security‑sensitive biological agent that an entity handles at a facility, means any of the following:

(a) the entity’s storage records for the agent;

(b) the entity’s risk assessment plan for the agent;

(d) any information:

(i) that the entity holds; and

(ii) disclosure of which could compromise the security of the agent.

Part 2—Public health surveillance

6 Prescribed intelligence agencies

For the purposes of paragraph 23(2)(b) of the Act, each of the following intelligence agencies is prescribed:

(a) the Australian Federal Police;

(b) the Australian Security Intelligence Organisation.

Part 3—Regulation of security‑sensitive biological agents

Division 1—The National Register

7 Content of National Register

For the purposes of paragraph 37(f) of the Act, the following particulars are prescribed in relation to an entity:

(a) if the entity’s head office is located at a place other than a facility where the entity handles security‑sensitive biological agents:

(i) the address of the entity’s head office; and

(ii) the entity’s postal address;

(b) the entity’s telephone number, fax number and email address;

(d) for each facility where the entity handles security‑sensitive biological agents:

(i) the geographic coordinates of the facility, expressed in terms of the Geocentric Datum of Australia 1994; and

(ii) the fax number of the facility; and

(iii) the name, telephone number, after hours telephone number and email address of the Responsible Officer for the facility; and

(iv) the name, telephone number, after hours telephone number and email address of the Deputy Responsible Officer for the facility;

(e) if the Secretary decides under section 49 of the Act to vary the National Register to take account of a reportable event in relation to the entity—details of the reportable event;

(f) if the Secretary decides under subsection 52(2) of the Act to vary the National Register on a temporary basis to take account of a reportable event in relation to the entity:

(i) details of the reportable event; and

(ii) a statement that the variation is temporary.

Division 2—Exempt entities

8 Purposes of this Division

For the purposes of paragraph 40(1)(b) of the Act, this Division prescribes entities to be exempt entities.

9 Law enforcement agencies

(1) A law enforcement agency is an exempt entity in relation to a security‑sensitive biological agent if the agency:

(a) handles the security‑sensitive biological agent only in the course of carrying out a function of the agency under a law of the Commonwealth, or of a State or Territory; and

(b) does not handle the security‑sensitive biological agent for the purpose of using it as a control sample for testing or carrying out diagnostic analysis.

(2) Each of the following is a law enforcement agency:

(a) the Australian Federal Police;

(b) a police force of a State or Territory;

(d) the Department administered by the Minister administering Part XII of the Customs Act 1901.

10 Depot and warehouse licence holders

(1) An entity that holds:

(a) a depot licence (within the meaning of Part IVA of the Customs Act 1901); or

(b) a warehouse licence (within the meaning of Part V of that Act);

is an exempt entity in relation to a security‑sensitive biological agent if the entity handles the security‑sensitive biological agent only in accordance with the licence.

(2) An entity that is permitted or required to do something under:

(a) paragraphs 77VA(2)(a) to (d) of the Customs Act 1901; or

(b) paragraphs 86(7)(a) to (d) of that Act;

is an exempt entity in relation to a security‑sensitive biological agent if the entity handles the security‑sensitive biological agent only in accordance with that permission or requirement.

11 Persons and animals affected by security‑sensitive biological agents

Persons affected by security‑sensitive biological agents

(1) A person who is affected by a security‑sensitive biological agent is an exempt entity in relation to that security‑sensitive biological agent while the person is affected by it.

Providing treatment to affected persons or animals

(2) An entity that provides treatment to a person or animal is an exempt entity in relation to a security‑sensitive biological agent if:

(a) the person or animal is or has been affected by the security‑sensitive biological agent; and

(b) the entity handles the security‑sensitive biological agent only while:

(i) the security‑sensitive biological agent is in the body of the person or animal; or

(ii) taking a sample from the person or animal for the purposes of the treatment.

Destroying affected animals

(3) An entity that destroys an animal is an exempt entity in relation to a security‑sensitive biological agent if:

(a) the animal is affected by the security‑sensitive biological agent; and

(b) the entity destroys the animal because the animal is affected by the security‑sensitive biological agent; and

Handling of bodies of affected deceased persons

(4) An entity that has the function of:

(a) examining, identifying, storing, transporting, burying or cremating the bodies of deceased persons; or

(b) preparing the bodies of deceased persons for burial or cremation;

is an exempt entity in relation to a security‑sensitive biological agent if:

(d) the entity handles the security‑sensitive biological agent only in the course of carrying out a function mentioned in paragraph (a) or (b) in relation to the person’s body.

12 Handling of mice to test for botulinum toxin

An entity that has the function of handling mice to test for the presence of botulinum toxin is an exempt entity in relation to botulinum toxin if the entity:

(a) handles the botulinum toxin only in the course of carrying out that function; and

(b) does not handle the botulinum toxin for the purpose of using it as a control sample for testing or carrying out diagnostic analysis.

Division 3—Reportable events for registered entities

Subdivision A—Unauthorised access

13 Unauthorised access

(1) This section applies if:

(a) a security‑sensitive biological agent is included in the National Register in relation to an entity and a facility; and

(b) a person at the facility enters a place where the security‑sensitive biological agent is handled.

(2) For the purposes of paragraph 48(1)(g) of the Act, access by the person to the security‑sensitive biological agent at that place is unauthorised if:

(a) the person is neither:

(i) authorised by the entity, in accordance with Part 3 of the SSBA Standards, to enter the place; nor

(ii) approved by the entity, in accordance with Part 3 of the SSBA Standards, to enter the place; or

(b) the person is so authorised or approved, but the person enters the place other than in accordance with the authorisation or approval.

Subdivision B—Other reportable events

14 Purposes of this Subdivision

For the purposes of paragraph 48(1)(h) of the Act, this Subdivision prescribes events in relation to registered entities.

15 Transfers of SSBAs—successful transfers

Transfers to other facilities of same entity

(1) Subregulation (2) applies if:

(a) a registered entity is included on the National Register in relation to a facility and a security‑sensitive biological agent; and

(b) the entity transfers the security‑sensitive biological agent from the facility to another facility of the entity; and

(d) the entity verifies, in accordance with Part 6 of the SSBA Standards, that the transport of the security‑sensitive biological agent to the other facility was successful.

(2) The event mentioned in paragraph (1)(d) is a reportable event for the entity.

Note: The event mentioned in paragraph (1)(b) is a reportable event for the entity under subparagraph 48(1)(e)(ii) of the Act.

Transfers to facilities of other entities

(3) Subregulation (4) applies if:

(a) a registered entity (the sending entity) is included on the National Register in relation to a facility (the sending facility) and a security‑sensitive biological agent; and

(b) another registered entity (the receiving entity) is included on the National Register in relation to another facility (the receiving facility) and the same security‑sensitive biological agent; and

(c) the sending entity transfers the security‑sensitive biological agent from the sending facility to the receiving facility; and

(d) the security‑sensitive biological agent is received at the receiving facility; and

(e) the receiving entity verifies, in accordance with Part 6 of the SSBA Standards, that the transport of the security‑sensitive biological agent to the receiving facility was successful.

(4) The event mentioned in paragraph (3)(e) is a reportable event for the receiving entity.

Note: The event mentioned in paragraph (3)(c) is a reportable event for the sending entity under subparagraph 48(1)(e)(i) of the Act.

16 Transfers of SSBAs—unsuccessful transfers

Transfers to other facilities of same entity

(1) Subregulation (2) applies if:

(a) a registered entity is included on the National Register in relation to a facility and a security‑sensitive biological agent; and

(b) the entity transfers the security‑sensitive biological agent from the facility to another facility of the entity; and

(d) the entity is unable to verify, in accordance with Part 6 of the SSBA Standards, that the transport of the security‑sensitive biological agent to the other facility was successful.

(2) The event mentioned in paragraph (1)(d) is a reportable event for the entity.

Note: The event mentioned in paragraph (1)(b) is a reportable event for the entity under subparagraph 48(1)(e)(ii) of the Act.

Transfers to facilities of other entities

(3) Subregulation (4) applies if:

(a) a registered entity (the sending entity) is included on the National Register in relation to a facility (the sending facility) and a security‑sensitive biological agent; and

(c) the sending entity transfers the security‑sensitive biological agent from the sending facility to the receiving facility; and

(d) the security‑sensitive biological agent is received at the receiving facility; and

(e) the receiving entity is unable to verify, in accordance with Part 6 of the SSBA Standards, that the transport of the security‑sensitive biological to the receiving facility was successful.

(4) The event mentioned in paragraph (3)(e) is a reportable event for the receiving entity.

Note: The event mentioned in paragraph (3)(c) is a reportable event for the sending entity under subparagraph 48(1)(e)(i) of the Act.

17 Transfers of SSBAs—SSBAs not received by expected time of delivery

Transfers to other facilities of same entity

(1) Subregulation (2) applies if:

(a) a registered entity is included on the National Register in relation to a facility and a security‑sensitive biological agent; and

(b) the entity arranges for the transfer of the security‑sensitive biological agent from the facility to another facility of the entity; and

(c) the entity notifies the other facility, in accordance with Part 6 of the SSBA Standards, of the expected time of delivery of the security‑sensitive biological agent to the other facility; and

(d) the security‑sensitive biological agent is not received at the other facility by the notified expected time of delivery.

(2) The event mentioned in paragraph (1)(d) is a reportable event for the entity.

Note 1: Transferring the security‑sensitive biological agent is a reportable event for the entity under subparagraph 48(1)(e)(ii) of the Act.

Note 2: Loss or theft of the security‑sensitive biological agent is a reportable event for the entity under paragraph 48(1)(f) of the Act.

(3) Subsection (2) does not apply if:

(a) the security‑sensitive agent is received at the other facility within 2 business days after the notified expected time of delivery; and

(b) at all times between the notified expected time of delivery and the receiving of the security‑sensitive biological agent, the entity knows that the security‑sensitive biological agent is not lost or stolen.

Transfers to facilities of other entities

(4) Subregulation (5) applies if:

(a) a registered entity (the sending entity) is included on the National Register in relation to a facility (the sending facility) and a security‑sensitive biological agent; and

(c) the sending entity arranges with the receiving entity for the transfer of the security‑sensitive biological agent from the sending facility to the receiving facility; and

(d) the sending entity notifies the receiving entity, in accordance with Part 6 of the SSBA Standards, of the expected time of delivery of the security‑sensitive biological agent to the receiving facility; and

(e) the security‑sensitive biological agent is not received at the receiving facility by the notified expected time of delivery.

(5) The event mentioned in paragraph (4)(e) is a reportable event for the receiving entity.

Note 1: Transferring the security‑sensitive biological agent is a reportable event for the sending entity under subparagraph 48(1)(e)(i) of the Act.

Note 2: Loss or theft of the security‑sensitive biological agent is a reportable event for the sending entity under paragraph 48(1)(f) of the Act.

(6) Subsection (5) does not apply if:

(a) the security‑sensitive agent is received at the receiving facility within 2 business days after the notified expected time of delivery; and

(b) at all times between the notified expected time of delivery and the receiving of the security‑sensitive biological agent, the receiving entity knows that the security‑sensitive biological agent is not lost or stolen.

18 Unauthorised handling etc.

An event mentioned in column 1 of an item of the following table is prescribed in relation to a registered entity that is included on the National Register in relation to a facility and a security‑sensitive biological agent, if:

(a) there are no circumstances mentioned in column 2 of the item; or

(b) the circumstances mentioned in column 2 of the item exist.

Reportable events
Item	Column 1 Event	Column 2 Circumstances
1	a person handles the security‑sensitive biological agent at the facility	(a) the person is neither: (i) authorised by the entity, in accordance with Part 3 of the SSBA Standards, to handle the security‑sensitive biological agent at the facility; nor (ii) approved by the entity, in accordance with Part 3 of the SSBA Standards, to handle the security‑sensitive biological agent at the facility; or (b) the person is so authorised or approved, but the handling is not in accordance with the authorisation or approval
2	a person attempts to handle the security‑sensitive biological agent at the facility	(a) the person is neither: (i) authorised by the entity, in accordance with Part 3 of the SSBA Standards, to handle the security‑sensitive biological agent at the facility; nor (ii) approved by the entity, in accordance with Part 3 of the SSBA Standards, to handle the security‑sensitive biological agent at the facility; or (b) the person is so authorised or approved, but the attempt is not in accordance with the authorisation or approval
3	a person attempts to access the security‑sensitive biological agent at the facility	the access is unauthorised under section 13
4	a person attempts to steal the security‑sensitive biological agent at the facility	none
5	the security‑sensitive biological agent is accidentally released during its handling at the facility	none
6	a person who has been to the facility is affected by the security‑sensitive biological agent as a result of the entity’s handling of the security‑sensitive biological agent at the facility	none
7	a person accesses sensitive information at the facility about the security‑sensitive biological agent Note: For sensitive information, see section 5.	(a) the person is neither: (i) authorised by the entity, in accordance with Part 3 of the SSBA Standards, to access the information; nor (ii) approved by the entity, in accordance with Part 3 of the SSBA Standards, to access the information; or (b) the person is so authorised or approved, but the access is not in accordance with the authorisation or approval
8	a person attempts to access sensitive information at the facility about the security‑sensitive biological agent	(a) the person is neither: (i) authorised by the entity, in accordance with Part 3 of the SSBA Standards, to access the information; nor (ii) approved by the entity, in accordance with Part 3 of the SSBA Standards, to access the information; or (b) the person is so authorised or approved, but the access is not in accordance with the authorisation or approval

19 Changes in particulars

The following events are prescribed in relation to a registered entity:

(a) a change to any of the following:

(i) the entity’s name;

(ii) if the entity’s head office is located at a place other than a facility where the entity handles security‑sensitive biological agents—the address of the entity’s head office, or the entity’s postal address;

(iii) the entity’s telephone number, fax number or email address;

(iv) the entity’s ABN, ACN or ARBN;

(b) any of the following events in relation to a facility where the entity handles security‑sensitive biological agents:

(i) a change to the name, location or fax number of the facility;

(ii) a change to the telephone number, after hours telephone number or email address of the Responsible Officer or the Deputy Responsible Officer for the facility;

(iii) the Responsible Officer for the facility ceases to be the Responsible Officer;

(iv) the Deputy Responsible Officer for the facility ceases to be the Deputy Responsible Officer;

(v) a Responsible Officer or Deputy Responsible Officer is appointed for the facility.

Subdivision C—When reports must be given

20 When reports must be given

For the purposes of subsection 48(3) of the Act, a registered entity that must give a report about a reportable event mentioned in column 1 of an item of the following table must give the report within the period mentioned in column 2 of the item.

When reports must be given
Item	Column 1 For a reportable event mentioned in …	Column 2 the report must be given within …
1	paragraph 48(1)(a) of the Act (entity starts to handle a security‑sensitive biological agent)	2 business days after the entity starts to handle the security‑sensitive biological agent.
2	(a) paragraph 48(1)(b) of the Act (entity disposes of its entire holdings of a security‑sensitive biological agent); or (b) paragraph 48(1)(c) of the Act (disposal of toxins resulting in less than a reportable quantity)	2 business days after the event occurs.
3	subparagraph 48(1)(d)(i) of the Act (entity starts to handle a security‑sensitive biological agent for a purpose not specified in the National Register)	2 business days after the entity starts to handle the security‑sensitive biological agent for that purpose.
4	subparagraph 48(1)(d)(ii) of the Act (entity stops handling a security‑sensitive biological agent for a purpose specified in the National Register)	2 business days after the entity stops handling the security‑sensitive biological agent for that purpose.
5	paragraph 48(1)(e) of the Act (entity transfers a security‑sensitive biological agent)	2 business days after the event occurs.
6	(a) paragraph 48(1)(f) of the Act (security‑sensitive biological agent is lost or stolen); or (b) paragraph 48(1)(g) of the Act (unauthorised access to a security‑sensitive biological agent)	2 business days after the entity becomes aware of the event.
7	section 15, 16 or 17 of this instrument (transfer of security‑sensitive biological agent)	2 business days after the event occurs.
8	section 18 of this instrument (unauthorised handling etc.)	2 business days after the entity becomes aware of the event.
9	section 19 of this instrument (change in particulars)	2 business days after the event occurs.

Subdivision D—Events that must be reported to police

21 Events that must be reported to police

(1) For the purposes of paragraph 48A(1)(b) of the Act, the following reportable events are prescribed:

(a) the event mentioned in paragraph 48(1)(g) of the Act;

(b) the event mentioned in subsection 16(2) or (4) of this instrument;

(d) the event mentioned in column 1 of item 1, 2, 3, 4, 7 or 8 of the table in section 18 of this instrument.

(2) For the purposes of subsection 48A(3) of the Act, the period is the period of 24 hours after the registered entity becomes aware of the event.

Division 4—Reportable events for entities that temporarily handle SSBAs

22 Unauthorised access

For the purposes of subparagraph 60AF(1)(b)(ii) of the Act, access is unauthorised if the access does not comply with Part 10 of the SSBA Standards.

23 When reports must be given

When reports must be given to Secretary

(1) For the purposes of subsection 60AF(2) of the Act, the period is the period of 2 business days after the entity becomes aware of the event.

When reports must be given to police

(2) For the purposes of subsection 60AH(3) of the Act, the period is the period of 24 hours after the entity becomes aware of the event.

Division 5—Identity cards

24 Identity cards

For the purposes of paragraph 64(2)(a) of the Act, an identity card issued to an inspector must contain the following:

(a) the full name of the inspector;

(b) a statement that the person to whom the card is issued is appointed under subsection 63(1) of the Act;

(c) for the photograph required under paragraph 64(2)(b) of the Act, an image showing the inspector’s full face, head and shoulders;

(d) the date the card was issued;

(e) the date the card expires.

Note: Paragraph 64(2)(b) of the Act provides that an identity card issued to an inspector must contain a recent photograph of the inspector.

Division 6—Confidentiality of information

25 Confidentiality of information

Intelligence agency

(1) For the purposes of paragraph 85(1)(a) of the Act, the Australian Security Intelligence Organisation is prescribed.

Law enforcement agencies

(2) For the purposes of paragraph 85(1)(b) of the Act, the following law enforcement agencies are prescribed:

(a) the Australian Federal Police;

(b) the police force of a State or Territory.

Endnotes

Endnote 1—About the endnotes

The endnotes provide information about this compilation and the compiled law.

The following endnotes are included in every compilation:

Endnote 1—About the endnotes

Endnote 2—Abbreviation key

Endnote 3—Legislation history

Endnote 4—Amendment history

Abbreviation key—Endnote 2

The abbreviation key sets out abbreviations that may be used in the endnotes.

Legislation history and amendment history—Endnotes 3 and 4

Amending laws are annotated in the legislation history and amendment history.

The legislation history in endnote 3 provides information about each law that has amended (or will amend) the compiled law. The information includes commencement details for amending laws and details of any application, saving or transitional provisions that are not included in this compilation.

The amendment history in endnote 4 provides information about amendments at the provision (generally section or equivalent) level. It also includes information about any provision of the compiled law that has been repealed in accordance with a provision of the law.

Editorial changes

The Legislation Act 2003 authorises First Parliamentary Counsel to make editorial and presentational changes to a compiled law in preparing a compilation of the law for registration. The changes must not change the effect of the law. Editorial changes take effect from the compilation registration date.

If the compilation includes editorial changes, the endnotes include a brief outline of the changes in general terms. Full details of any changes can be obtained from the Office of Parliamentary Counsel.

Misdescribed amendments

A misdescribed amendment is an amendment that does not accurately describe how an amendment is to be made. If, despite the misdescription, the amendment can be given effect as intended, then the misdescribed amendment can be incorporated through an editorial change made under section 15V of the Legislation Act 2003.

If a misdescribed amendment cannot be given effect as intended, the amendment is not incorporated and “(md not incorp)” is added to the amendment history.

Endnote 2—Abbreviation key

ad = added or inserted	o = order(s)
am = amended	Ord = Ordinance
amdt = amendment	orig = original
c = clause(s)	par = paragraph(s)/subparagraph(s)
C[x] = Compilation No. x	/sub‑subparagraph(s)
Ch = Chapter(s)	pres = present
def = definition(s)	prev = previous
Dict = Dictionary	(prev…) = previously
disallowed = disallowed by Parliament	Pt = Part(s)
Div = Division(s)	r = regulation(s)/rule(s)
ed = editorial change	reloc = relocated
exp = expires/expired or ceases/ceased to have	renum = renumbered
effect	rep = repealed
F = Federal Register of Legislation	rs = repealed and substituted
gaz = gazette	s = section(s)/subsection(s)
LA = Legislation Act 2003	Sch = Schedule(s)
LIA = Legislative Instruments Act 2003	Sdiv = Subdivision(s)
(md) = misdescribed amendment can be given	SLI = Select Legislative Instrument
effect	SR = Statutory Rules
(md not incorp) = misdescribed amendment	Sub‑Ch = Sub‑Chapter(s)
cannot be given effect	SubPt = Subpart(s)
mod = modified/modification	underlining = whole or part not
No. = Number(s)	commenced or to be commenced

Endnote 3—Legislation history

Name	Registration	Commencement	Application, saving and transitional provisions
National Health Security Regulations 2018	31 Aug 2018 (F2018L01247)	1 Sept 2018 (s 2(1) item 1)
Statute Law Amendment (Prescribed Forms) Regulations 2024	15 Mar 2024 (F2024L00294)	Sch 1 (item 50): 20 Mar 2024 (s 2(1) item 1)	—

Endnote 4—Amendment history

Provision affected	How affected
Part 1
s 2.....................	rep LA s 48D
s 4.....................	rep LA s 48C
Part 3
Division 5
s 24....................	am F2024L00294
Schedule 1................	rep LA s 48C