Health Insurance (Accredited Pathology Laboratories

This is the Health Insurance (Accredited Pathology Laboratories—Approval) Principles 2017.

This instrument is made under subsection 23DNA(1) of the Act.

(1) These Principles apply to the exercise by the Minister of a power under section 23DN of the Act on and after commencement in relation to:

(a) an application for approval of premises as an accredited pathology laboratory whether that application was made before or after commencement; and

(b) the exercise by the Minister of a power to revoke or vary an approval of premises whether the approval was given before or after commencement.

Note: See subsection 23DN(6A) of the Act.

5 Interpretation

(1) Words in this instrument have, unless they are otherwise defined, the same meaning as in the Act.

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

 accredited pathology laboratory;

 approved pathology authority;

 approved pathology practitioner;

 medical practitioner;

 pathology service;

 pathology services table.

(2) In these Principles:

accreditation action means an independent body’s grant, refusal to grant or revocation of accreditation, however any of these actions are described, in relation to the rendering of some or all of the pathology services at premises.

accreditation materials means each document mentioned in Schedule 1, published in the year mentioned for the document.

Act means the Health Insurance Act 1973.

advisory report means a report provided by an independent body in accordance with subsection 12(3).

assessment report means a report provided by an independent body or a special adviser in accordance with section 9.

category means a category under section 17.

designated person means a person who is designated in an application for approval under section 23DN of the Act as the person responsible for a premises’ compliance with relevant standards.

group of pathology testing means a group of items in the pathology services table.

independent body means:

(a) NATA; and

(b) any other organisation approved under subsection (3) by the Minister.

NATA means the National Association of Testing Authorities Australia (ACN 004 379 748).

NPAAC means the National Pathology Accreditation Advisory Council established under subsection 9(1) of the National Health Act 1953.

pathologist means a medical practitioner recognised as a specialist for the purposes of the Act in relation to any of the specialties listed in Column 3, Item 113 of Schedule 4 of the Health Insurance Regulations 1975, or regulations made to replace those regulations.

premises means premises or a part of any premises used or proposed to be used as a pathology laboratory.

relevant standards means standards set out in the accreditation materials and in section 18.

scope of practice means the discipline and areas of testing in which a person has:

(a) been trained and successfully examined or assessed as competent by the relevant College, professional society, or credentialing body; and

(b) met current Continuing Professional Development and recency of practice requirements.

special adviser means a person appointed by the Minister to advise the Minister on the standards of pathology services rendered at premises.

State includes a Territory.

State accreditation means accreditation under an accreditation system under the written law of a State or under a State Government administrative arrangement to provide accreditation, however described, for provision of pathology services.

undertaking means an undertaking given under section 23DC or section 23DF of the Act.

(3) Subject to subsection (4), the Minister may approve an organisation as an independent body in relation to a category or categories of laboratory for the purposes of these Principles.

(4) In making a decision under subsection (3) the Minister must take into account that:

(a) ordinarily an organisation other than NATA should be approved only if there is a high level of confidence that the organisation is a suitable organisation to act as an independent body for the purposes of these Principles; and

(b) the objects of these Principles should not be negatively affected by competitive pressures on any independent body.

(5) A reference in these Principles to the revocation of accreditation by an independent body or to revocation of State accreditation includes, without limitation:

(a) action taken by the independent body;

(b) action taken in a State accreditation process;

(d) the operation of rules in the State accreditation process;

that has the effect of revoking, cancelling, suspending or rendering inoperative the accreditation, or an aspect of the accreditation, no matter what term is used to describe that action.

(6) In these Principles a reference to an application for approval under section 23DN of the Act includes without limitation an application for a variation of an approval:

(a) by adding a kind of service not covered by the approval; or

(b) by changing the category covered by the approval; or

Part 2—General

6 Purpose and objects of Principles

(1) These are the Principles to be applied by the Minister in exercising his or her powers under section 23DN of the Act:

(a) to approve in principle premises as an accredited pathology laboratory; and

(b) to refuse to approve premises as an accredited pathology laboratory; and

(2) The objects of these Principles are to:

(a) support the diagnosis and treatment of illness in the community by providing Medicare benefits in relation to pathology services that provide reliable results; and

(b) reduce the risk of misdiagnosis through misleading results being provided by pathology services that do not provide reliable results; and

(d) protect limited public funds available for Medicare benefits by only providing Medicare benefits in relation to pathology services that provide reliable results; and

(e) ensure that, as far as practicable, premises will be approved in principle, and will remain approved under section 23DN of the Act, for the kind of pathology services and for the category, only if it is established with a high level of confidence that the pathology services to be rendered, or rendered, at the premises meet, and can be expected to continue to meet, relevant standards for those kinds of services and for that category.

7 Weight to be given to views of independent body or special adviser

(1) When considering the making of a decision under section 23DN of the Act in relation to premises, the Minister must take into account:

(a) the most recent advisory report, if any, in relation to the premises; and

(b) the most recent assessment report, if any, in relation to the premises; and

(2) The Minister may take into account an advisory report, an assessment report or an accreditation action which is not the most recent.

(3) Where there is a difference between:

(a) views expressed or implied by an independent body in its advisory report or assessment report, or by its accreditation action, or by a special adviser in its assessment report; and

(b) any other person’s view obtained and put forward by an applicant for approval or by the holder of an approval under section 23DN of the Act;

the Minister should generally give greater weight to the views of the independent body or the special adviser, as appropriate.

8 Action may be taken despite appeal or challenge

(1) The Minister must continue to apply the Principles, including taking into account a relevant advisory report, assessment report or accreditation action, even if a person affected by the report or accreditation action is seeking review by the independent body or special adviser concerned, or by a judicial or other review body, of the report or accreditation action.

(2) If:

(a) the Minister has made a decision under section 23DN of the Act after taking into account an advisory report, assessment report or accreditation action of an independent body, or an assessment report of a special adviser; and

(b) the report or accreditation action is later varied, or a judicial or other body has set aside or varied the report or accreditation action;

the Minister may, but is not obliged to, review the decision under section 23DN of the Act.

(3) If:

(a) the circumstances referred to in paragraphs (2)(a) and (b) occur; and

(b) the Minister does not review the decision under section 23DN of the Act;

the Minister must take into account the circumstances referred to in paragraph (2)(b) when considering a new application for approval under section 23DN of the Act.

9 Assessment report by independent body or special adviser

(1) An assessment report in relation to premises must:

(a) be in writing; and

(b) be dated; and

(d) identify the independent body or special adviser providing the report; and

(e) be certified by an officer of the independent body or by the special adviser to contain a true report of the views of the individuals who participated in the assessment.

(2) An assessment report:

(a) must state whether or not it has been established with a high level of confidence that the pathology services to be rendered or rendered at the premises subject to the report meet, and can be expected to continue to meet, the relevant standards; and

(b) if so established, must also state:

(i) by reference to items in the pathology services table, or by reference to groups of items in the pathology services table, the kind of pathology services in respect of which the premises should be approved or should remain approved; and

(ii) the category to which the premises should be allocated or remain allocated; and

(iii) the period of time for which the premises can be expected to meet relevant standards; and

10 Other matters taken into account in making decisions

(1) When making a decision under section 23DN of the Act in relation to premises, without limiting other sections in these Principles, the Minister may also take into account:

(a) any other report, assessment or decision about accreditation which has been prepared or made at any time by an independent body or a special adviser or in the course of State accreditation which:

(i) relates to the provision of pathology services at the premises; or

(ii) relates to any persons employed or to be employed in or otherwise associated with or to be associated with the provision of pathology services at the premises; and

(b) any circumstance that gives the Minister reasonable cause to believe that an approved pathology authority or an approved pathology practitioner who is, or may be, associated with the operation of the laboratory at the premises has breached an undertaking at any time; and

(2) Paragraphs (1)(a) and (1)(b) apply whether or not the current applicant for approval or holder of approval was associated with the premises at the time of the report, assessment or decision or at the time of the events taken into account in the report, assessment or decision or at the time the circumstance arose.

Part 3—Approval of premises

11 Approval of premises

(1) In the absence of exceptional circumstances, the Minister must not approve in principle premises unless the Minister is satisfied with a high level of confidence that:

(a) the pathology services to be rendered at the premises will meet relevant standards for:

(i) the kinds of services to be rendered; and

(ii) the category; and

(b) without limiting paragraph (a), the premises comply with the relevant requirements of:

(i) the Act; and

(ii) these Principles.

(2) Subject to section 12, the Minister must only consider an application for approval of premises under section 23DN of the Act if the Minister is provided with an assessment report which is the most recent assessment report in relation to the premises.

(3) In the absence of exceptional circumstances, the Minister must not approve in principle premises if within the 6 months preceding the application the last accreditation action in relation to the premises the subject of the application was:

(a) a refusal by an independent body to grant an accreditation for pathology services rendered at the premises in relation to the kinds of services or to the category subject to the application before the Minister; or

(b) a revocation by an independent body of an accreditation held for pathology services rendered at premises in relation to the kinds of services or to the category subject to the application before the Minister.

(4) In the absence of exceptional circumstances, the Minister must not give an approval in principle unless the Minister is satisfied that the assessment report referred to in subsection (2) supports the approval of the premises as an accredited pathology laboratory for:

(a) the kind of services; and

(b) the category;

covered by the application.

(5) If premises are not approved in principle on account of the operation of subsection (4), and the applicant amends the application in relation to:

(a) the kind of services; or

(b) the category;

covered by the application, the Minister may consider and deal with the amended application in accordance with these Principles as if it were an original application.

12 Approval in absence of assessment report

(1) If no independent body or special adviser has provided an assessment report in relation to premises, the Minister may consider an application for approval under section 23DN of the Act in relation to those premises and otherwise deal with the application taking into account these Principles if:

(a) subsection (2) applies; and

(b) an advisory report is provided with the application.

(2) This subsection applies if an application for approval in relation to premises under section 23DN of the Act is made in relation to:

(a) a kind of service; or

(b) a category;

not subject to an approval in principle or an approval under section 23DN of the Act held by the applicant for those premises at the time of making the application.

(3) In the absence of exceptional circumstances, the Minister must approve in principle an application which relies on this section if the application is supported by a report from an independent body which states:

(a) that a representative of the independent body has visited the premises; and

(b) that the independent body confirms that there is an appropriately equipped pathology laboratory at the premises; and

(c) that the independent body is satisfied with a high level of confidence, taking into account the arrangements in relation to the operation of the premises, that:

(i) the premises can be expected to meet relevant standards for a 6 month period; and

(ii) the premises are, or will be, appropriately staffed with persons to render, and persons to direct, control and supervise, the pathology services to be rendered at the premises; and

(iii) the laboratory is, or will be at the relevant time, participating in a quality assurance program of an independent quality assurance body designed to ensure that the laboratory operates in accordance with the accreditation materials applicable to the kinds of pathology services to which approval of the premises would relate; and

(d) the kind of pathology services in respect of which the premises should be approved (identified by reference to items in the pathology services table or by reference to groups of items in the pathology services table); and

(e) the category to which the premises should be allocated.

Note: The independent quality assurance body mentioned in subparagraph (3)(c)(iii) might not be an independent body within the meaning of subsection 5(2).

13 Approval where there is a State accreditation system

(1) This section applies if the State in which the premises are located has an accreditation system under which pathology laboratories may obtain accreditation for the rendering of pathology services of the kind to which the application relates.

(2) When making a decision under section 23DN of the Act, the Minister must consider, in relation to the premises, the following matters:

(a) whether the premises have State accreditation; and

(b) if the premises have State accreditation, the services for which the accreditation is granted, the basis on which the accreditation was conferred and the period for which the accreditation operates; and

(i) has been revoked; or

(ii) has been refused; or

(iii) has not been sought; or

(iv) has not been renewed; and

(d) for premises to which paragraph (2)(c) applies, the reasons for the circumstance.

14 Period of approval

(1) In the absence of exceptional circumstances, the Minister must not determine a period of approval which exceeds:

(a) the period of time for which the laboratory can be expected to meet relevant standards stated in the most recent assessment report; or

(b) the period of accreditation under the most recent accreditation action.

(2) Subject to subsection (3), the Minister must not grant an approval in reliance on an advisory report for longer than 6 months.

(3) In exceptional circumstances, the Minister may grant extensions to an approval granted in reliance on an advisory report provided that:

(a) each extension is supported by a further advisory report; and

(b) the cumulative period of those extensions does not exceed 6 months.

Note: See also paragraph 23DN(2A)(c) of the Act.

15 Revocation of approval

(1) In the absence of exceptional circumstances, the Minister must revoke an approval of premises if one or more of the following circumstances applies:

(a) the most recent assessment report states that it has not been established with a high level of confidence that the pathology services rendered at the premises covered by the approval meet, and can be expected to continue for the remainder of the period of the approval to meet, relevant standards;

(b) the most recent accreditation action in relation to the premises is revocation;

(c) State accreditation relevant to pathology services covered by the approval has been revoked or has not been renewed and the holder of the approval has not provided the Minister with a satisfactory explanation for the revocation or non‑renewal of the State accreditation;

(d) the Minister has formed the view that the premises no longer meet the requirements for approval under subsection 11(1).

(2) The Minister must act in accordance with this section within 28 days of learning that any of the circumstances in subsection (1) applies.

(3) This section does not limit the considerations which the Minister may take into account when considering whether to revoke an approval under section 23DN of the Act.

16 Variation of approval

(1) In the absence of exceptional circumstances, the Minister must make an appropriate variation to an approval of premises under section 23DN of the Act if one or more of the following circumstances applies:

(b) an independent body varies an accreditation relating to the kind of pathology services that may be rendered at the premises by removing a service from that accreditation;

(c) State accreditation relevant to any of the services covered by the approval in relation to the premises has been revoked or has not been renewed and the Minister has not been provided by the holder of the approval with a satisfactory explanation of the revocation or non‑renewal of the State accreditation.

(2) The Minister must act in accordance with this section within 28 days of learning that any of the circumstances in subsection (1) applies.

(3) This section does not limit the considerations which the Minister may take into account when considering whether to vary an approval under section 23DN of the Act.

Part 4—Categories of premises

17 Allocation of categories

(1) The categories of accreditation of pathology laboratories for the purposes of section 23DN of the Act and the criteria applicable to each of those categories are set out in the following table:

Item	Category	Criteria
1	Category GX (General)	Premises comprising a laboratory, or a number of co‑located laboratories, that: (a) is under the full‑time onsite direction and control of a designated person, who is a pathologist; and (b) renders services in 1 or more groups of pathology testing under the full‑time onsite supervision of a pathologist (whether or not the designated person) with the relevant scope of practice.
2	Category GY (General)	Premises comprising a laboratory, or a number of co‑located laboratories, that: (a) is related by an appropriate arrangement to a GX laboratory; and (b) is under the direction and control of the designated person of the related GX laboratory; and (c) renders services in 1 or more groups of pathology testing under the full‑time onsite supervision of a pathologist with the relevant scope of practice; whether or not the premises also renders services in 1 or more groups of pathology testing under the supervision of a pathologist with the relevant scope of practice who is situated in: (d) the related GX laboratory (whether or not the pathologist is the designated person); or (e) another GY laboratory that is related to that GX laboratory.
3	Category B (Branch)	Premises comprising a laboratory, or a number of co‑located laboratories, that: (a) is related by an appropriate arrangement to a GX laboratory or GY laboratory; and (b) is under the direction and control of the same designated person as the related laboratory; and (c) renders services in 1 or more groups of pathology testing under the supervision of a pathologist (whether or not the designated person) from a laboratory within the pathology network.
4	Category M (Medical)	Premises comprising a laboratory that: (a) is under the full‑time onsite direction, control and supervision of a designated person, who is a medical practitioner; and (b) renders a limited range of pathology testing only for the patients of a medical practice that: (i) is operated by, or employs, the designated person; and (ii) is co‑located with the laboratory.
5	Category S (Specialised)	Either of the following: (a) premises comprising a laboratory that: (i) is under the full‑time onsite direction, control and supervision of a designated person, who is: (A) a medical practitioner with specialised scope of practice; and (B) not a pathologist; and (ii) renders a limited range of pathology testing: (A) for a target patient population or of a specialised nature; and (B) that is restricted to the field of pathology testing directly related to the scope of practice of the designated person; (b) premises comprising a laboratory that: (i) operates as a branch of a laboratory which meets the criteria in paragraph (a); and (ii) is under the direction, control and supervision of the designated person of that laboratory.

(2) In the table in subsection (1), appropriate arrangement means a written arrangement that includes provision for the direction, control and supervision of the relevant laboratory.

(3) The category of accreditation allocated to premises that is specified by the Minister in an approval under section 23DN of the Act must be the category set out in the table in subsection (1) that is appropriate to the premises having regard to the criteria applicable to that category.

Note: For the purpose of determining the fee payable for an application for approval as a particular category of laboratory, the categories set out below correspond to the categories specified in section 6 of the Health Insurance (Pathology) (Fees) Act 1991:

(a) category GX—paragraph 6(3)(a);

(b) category GY—paragraph 6(3)(b);

(d) category M—paragraph 6(3)(d);

(e) category S—paragraph 6(3)(d).

18 Standards of direction, control and supervision of premises required

(1) Premises must be under the direction, control and supervision of a designated person, who:

(a) possesses appropriate qualification; and

(b) is competent; and

to fulfil their obligations under this section.

(2) The designated person is responsible for premises’ compliance with relevant standards.

(3) Without limiting subsection (2), the designated person is responsible for compliance with the standards of direction, control and supervision that apply to the relevant category of laboratory under the Requirements for Supervision in the Clinical Governance of Medical Pathology Laboratories (Fifth Edition 2018), including in relation to:

(a) the clinical governance of the laboratory; and

(b) oversight and management of the laboratory’s staff and processes to ensure ethical patient care and the provision of accurate and timely test results.

(4) The designated person may only supervise pathology testing within his or her scope of practice.

(5) The responsibilities of the designated person for premises under this section may be delegated, but only in accordance with the Requirements for Supervision in the Clinical Governance of Medical Pathology Laboratories (Fifth Edition 2018).

Note: The Requirements for Supervision in the Clinical Governance of Medical Pathology Laboratories (Fifth Edition 2018) is listed in Schedule 1.

Part 5—Transitional arrangements

19 Continued application of the old Principles to certain laboratories

(1) In this section:

IVF testing means testing related to the diagnosis and treatment of fertility issues.

listed premises means a premises that, immediately before 1 August 2019, was subject to an approval under section 23DN of the Act identified by any of the following Accredited Pathology Laboratory numbers:

(a) APL 30498;

(b) APL 39161;

(d) APL 39395;

(e) APL 38273;

(f) APL 30322.

old Principles means these Principles, as in force immediately before 1 August 2019.

Application of old Principles to approvals of certain Category S laboratories in effect immediately before 1 August 2019

(2) Despite section 4, the old Principles continue to apply in relation to premises if:

(a) an approval of the premises under section 23DN of the Act was in effect immediately before 1 August 2019; and

(b) the category of accreditation specified in the approval was, immediately before 1 August 2019, Category S; and

(3) Subsection (2) ceases to apply in relation to premises on the earlier of the following:

(a) when the approval of the premises:

(i) is revoked; or

(ii) is varied such that Category S is no longer specified; or

(iii) is varied such that IVF testing is no longer specified; or

(iv) ceases to have effect on expiration of the period specified in the approval as the period for which the approval is to have effect;

(b) 1 January 2021.

Application of old Principles to new applications for approval by certain Category S laboratories

(4) Subsection (5) applies in relation to premises only if:

(a) at any time in the three months before 1 August 2019, an approval (the old approval) of the premises under section 23DN of the Act had been in effect; and

(b) the category of accreditation specified in the old approval was Category S; and

(5) If:

(a) before 1 January 2021, an application (the new application) is made for approval of premises under section 23DN of the Act; and

(b) the category of accreditation sought in the new application is Category S; and

(d) the new application specifies that the old Principles are to apply;

despite section 4, the old Principles apply to the premises in relation to:

(e) the approval or refusal of the new application; and

(f) if the new application is approved:

(i) the period of the approval; and

(ii) any revocation of the approval; and

(iii) any variation of the approval.

(6) Subsection (5) ceases to apply in relation to premises on 1 January 2021.

Application of old Principles to approvals of listed premises

(7) Despite section 4, the old Principles continue to apply in relation to listed premises.

(8) Subsection (7) ceases to apply in relation to listed premises on the earlier of the following:

(a) when the approval of the premises:

(i) is revoked; or

(ii) ceases to have effect on expiration of the period specified in the approval as the period for which the approval is to have effect;

(b) 1 January 2021.

Application of old Principles to new applications for approval of listed premises

(9) If:

(a) before 1 January 2021, an application (the new application) is made for approval of listed premises under section 23DN of the Act; and

(b) the category of accreditation for which approval is sought in the new application is the same as was specified in the approval of the premises in effect immediately before 1 August 2019; and

(c) the kind of pathology services for which approval is sought in the new application is the same as was specified in the approval of the premises in effect immediately before 1 August 2019; and

(d) the new application specifies that the old Principles are to apply;

despite section 4, the old Principles apply to the listed premises in relation to:

(e) the approval or refusal of the new application; and

(f) if the new application is approved:

(i) the period of the approval; and

(ii) any revocation of the approval; and

(iii) any variation of the approval.

(10) Subsection (9) ceases to apply in relation to listed premises on 1 January 2021.

Schedule 1—Accreditation materials

Note: See definition of accreditation materials in subsection 5(2).

NPAAC materials

Item	Material	Publication year
1	Requirements for the Estimation of Measurement Uncertainty	2007
2	Guidelines for Approved Pathology Collection Centres (Requirements for Medical Pathology Specimen Collection) (Third Edition 2013)	2013
3	Requirements for Cytogenetic Testing (Third Edition 2013)	2013
4	Requirements for Information Communication (Third Edition 2013)	2013
5	Requirements for Laboratory Testing for Human Immunodeficiency Virus (HIV) and Hepatitis C Virus (HCV) (Third Edition 2013)	2013
6	Requirements for Medical Testing of Human Nucleic Acids (Second Edition 2013)	2013
7	Requirements for Medical Testing of Microbial Nucleic Acids (Second Edition 2013)	2013
8	Requirements for the Facilities and Operation of Mortuaries (Third Edition 2013)	2013
9	Requirements for the Packaging and Transport of Pathology Specimens and Associated Materials (Fourth Edition 2013)	2013
10	Requirements for the Performance of Anatomical Pathology Cut‑Up (Fourth Edition 2013)	2013
11	Performance Measures for Australian Laboratories Reporting Cervical Cytology (Third Edition 2015)	2015
12	Requirements for Procedures Related to the Collection, Processing, Storage and Issue of Human Haemopoietic Progenitor Cells (Fifth Edition 2015)	2015
13	Requirements for Human Medical Genome Testing Utilising Massively Parallel Sequencing Technologies (First Edition 2017)	2017
14	Requirements for Laboratories Reporting Tests for the National Cervical Screening Program (Second Edition 2019)	2019
15	Requirements for Semen Analysis (First Edition 2017)	2017
16	Requirements for Transfusion Laboratory Practice (Fourth Edition 2019)	2019
17	Requirements for Medical Pathology Services (Third Edition 2018)	2018
18	Requirements for Quality Control, External Quality Assurance and Method Evaluation (Sixth Edition 2017)	2018
19	Requirements for Supervision in the Clinical Governance of Medical Pathology Laboratories (Fifth Edition 2018)	2018
20	Requirements for the Development and Use of In‑House In Vitro Diagnostic Devices (Fourth Edition 2017)	2018
21	Requirements for the Retention of Laboratory Records and Diagnostic Material (Seventh Edition 2017)	2018
22	Requirements for Validation of Self‑Collected Vaginal Swabs for use in the National Cervical Screening Program (First Edition 2019)	2019

Note The documents mentioned could in 2018 be viewed on NPAAC’s website, maintained by the Department of Health (http://www.health.gov.au/npaac).

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 the amendment to be made. If, despite the misdescription, the amendment can be given effect as intended, the amendment is incorporated into the compiled law and the abbreviation “(md)” added to the details of the amendment included in the amendment history.

If a misdescribed amendment cannot be given effect as intended, the abbreviation “(md not incorp)” is added to the details of the amendment included in 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
Health Insurance (Accredited Pathology Laboratories—Approval) Principles 2017	28 Sept 2017 (F2017L01291)	29 Sept 2017 (s 2)
Health Insurance (Accredited Pathology Laboratories—Approval) Amendment Instrument (No. 1) 2018	28 June 2018 (F2018L00933)	Sch 2: 1 Dec 2018 (s 2(1) item 3) Remainder: 29 June 2018 (s 2(1) items 1, 2)	—
Health Insurance (Accredited Pathology Laboratories—Approval) Amendment Instrument (No. 2) 2018	29 Nov 2018 (F2018L01633)	Sch 1: 1 Dec 2018 (s 2(1) item 2) Sch 2: 1 Aug 2019 (s 2(1) item 3)	—
Health Insurance (Accredited Pathology Laboratories—Approval) Amendment Instrument (No. 1) 2019	31 July 2019 (F2019L01030)	Sch 1: 1 Aug 2019 (s 2(1) item 2)	—
Health Insurance (Accredited Pathology Laboratories–Approval) Amendment Instrument (No. 2) 2019	26 Sept 2019 (F2019L01278)	Sch 1: 27 Sept 2019 (s 2(1) item 2)	—

Endnote 4—Amendment history

Provision affected	How affected
Part 1
s 2.....................	rep LA s 48D
s 4.....................	(2) rep LA s 48C
s 5.....................	am F2018L00933; F2018L01633
Part 2
s 7.....................	am F2018L00933
s 8.....................	am F2018L00933
s 9.....................	am F2018L00933
s 10....................	am F2018L00933
Part 3
s 11....................	am F2018L00933
s 12....................	am F2018L00933
Part 4
s 17....................	am F2018L00933; F2018L01633
s 18....................	rs F2018L00933; F2018L01633
Part 5
Part 5...................	ad F2019L01030
s 19....................	ad F2019L01030
Schedule 1
Schedule 1................	rs F2018L00933
	am F2018L01633; F2019L01278
Schedule 2
Schedule 2................	am F2018L00933
	rep F2018L00933