ADVANCE MEDICAL DIRECTIVES ACT
Table of Provisions (13)
Statutory Text (13 Articles)
CHAPTER 658
ADVANCE MEDICAL DIRECTIVES ACT
AN ACT to regulate the drawing of, the registration, recognition
and implementation of advance medical directives and any matter
ancillary thereto.
*
ACT No. XII of 2026
(1)
The short title of this Act is the Advance Medical
Directives Act.
(2)
This Act shall come into force on such date or dates as the
Minister may by notice in the Gazette establish and different dates may
be so established for different provisions and, or different purposes of
this Act.
(Article 4(5))
Model Form of Advance Medical Directive
PART I – IDENTIFICATION OF THE APPEARER
I, the undersigned
Full name and surname:...................................................................
Son / Daughter of:.............................................................. (father)
and.............................................................. (mother,
née..........................................................................)
Born in:..............................................................
On:.....................................................................
Residing in (locality):.....................................................................
Holder
of
Identity
Card
/
Passport
No.:..........................................................................
hereby declare that I am making this Advance Medical Directive
freely, voluntarily and after having been provided with adequate
medical information.
PART II – CAPACITY AND MEDICAL DISCUSSION
I declare that
☐ I have discussed this Advance Medical Directive with a medical
practitioner;
☐ I have been informed in a clear and comprehensible manner of
the nature and consequences of the refusals contained herein;
☐ I understand that this directive applies only if at the material
time, I lack capacity to give or refuse consent.
PART III – CIRCUMSTANCES OF APPLICATION
This Advance Medical Directive shall apply only in the event that
☐ I lack capacity to make or communicate decisions regarding my
medical treatment; and
☐ I am in one (1) or more of the following situations (tick as
applicable)
☐ Terminal illness with no reasonable prospect of recovery;
☐ Permanent unconsciousness, persistent vegetative state, or
minimally conscious state with no reasonable prospect of recovery;
☐ Advanced, irreversible condition resulting in total dependency
and severe suffering with no prospect of meaningful improvement.
PART IV – REFUSAL OF MEDICAL TREATMENT
If the circumstances described in Part III apply, I hereby refuse the
following medical treatments (tick as applicable)
☐ Cardiopulmonary resuscitation (CPR);
☐ Mechanical ventilation;
☐ Artificial nutrition;
☐ Artificial hydration;
☐ Renal replacement therapy (dialysis);
☐ Antibiotic treatment primarily aimed at prolonging life;
☐ Any other specified treatment
I understand that refusal of the above treatments may result in my
death.
The appearer
appoints (Name and Surname)
................................................... (Identity Card No.) in order that the
authorities notify him/her, if required, however the said person may not
alter or vary the directive of the appearer.
PART V – RELIEF FROM PAIN AND COMFORT CARE
Notwithstanding any refusal of medical treatment expressed in this
Advance Medical Directive, I instruct that appropriate palliative and
comfort care shall always be provided, in accordance with established
standards of medical care.
In particular, I instruct that treatment for the alleviation of pain,
suffering, breathlessness, anxiety or any other discomfort shall be
provided, even if such treatment may incidentally shorten my life.
Unless I state otherwise below, I consent to the provision of pain
relief and comfort measures as medically indicated
.........................................................................................................
(If no limitation is expressed above, full palliative care shall be
provided.)
PART VI – REVIEW AND CONSISTENCY
I understand that
☐ I may revoke or amend this directive at any time while I have
capacity;
☐ Any oral revocation made in the presence of a medical
practitioner and at least one (1) witness shall be valid;
☐ Any subsequent conduct clearly inconsistent with this directive
may affect its validity or applicability in accordance with the Advance
Medical Directives Act.
PART VII – MEDICAL PRACTITIONER CERTIFICATION
I, the undersigned medical practitioner
Name and surname:.........................................................................
Professional registration number:...................................................
Speciality / Practice:.......................................................................
certify that
☐ I have discussed advanced medical planning with the appearer;
☐ In my professional opinion, the appearer demonstrated capacity
at the time of signing this directive;
☐ The appearer demonstrated understanding of the nature and
consequences of the refusal contained herein.
Signature of medical practitioner:...................................................
Name and surname:.........................................................................
Registration number:.................................
STAMP
Date:..........................................................
PART VIII – DECLARATION BY THE APPEARER (TO BE
MADE BEFORE A NOTARY)
I declare that I have read and understood the contents of this
Advance Medical Directive and that it reflects my present, free and
settled wishes.
This declaration is made and signed by me in the presence of a
notary for the purposes of authentication in accordance with the
Advance Medical Directives Act.
Signature of appearer:......................................................................
Date:..............................................
PART IX – NOTARIAL AUTHENTICATION
I, the undersigned notary, hereby certify that the appearer
personally appeared before me on the date hereunder indicated, and
that I verified his/her identity in accordance with law, and that the
appearer signed the declaration contained in Part VIII in my presence
after acknowledging and reconfirming that the contents of this
Advance Medical Directive express his/her present and settled wishes.
Signature of Notary:..............................................................
Name and surname:.........................................................................
STAMP
Date:..............................................
In this Act, unless the context otherwise requires
"advance medical directive" or "directive" means a prior
decision made by an appearer while having capacity, by which
he refuses specified medical treatment in defined future
circumstances when the appearer lacks capacity to give
consent;
"appearer" means the person making an advance
medical directive in accordance with this Act;
"material time" means the time at which a decision
regarding the provision, withholding or withdrawal of medical
treatment is required to be taken in respect of the appearer;
"medical practitioner" shall have the same meaning
assigned to it in the Mental Health Act;
* Not yet in force.
"medical records" means all documents containing data,
assessments and information of any kind relating to a patient’s
situation and clinical development throughout the treatment
process, and includes the electronic health record of the patient;
"Minister" means the Minister responsible for the
promotion of equality in consultation with the Minister
responsible for health;
(1)
Any person who has attained the age of eighteen (18)
years and has mental capacity may make an advance medical directive
in accordance with this Act.
(2)
A directive shall include refusal of specified medical
treatments in defined circumstances.
(3)
Any stipulation contained in a directive which requires the
omission, instruction or practice that is contrary to law shall be null
and void.
PART II
Preparation, Form and Legal Effect of
Advance Medical Directives
(1)
An advance medical directive shall be prepared
following consultation between the appearer and a medical
practitioner.
(2)
The medical practitioner shall assist the appearer in
advanced medical planning and shall ensure that the appearer is
adequately informed of the nature and clinical implications of the
refusals contained in the directive.
(3)
The medical practitioner shall assess the mental capacity of
the appearer at the time of the preparation of the directive and shall
certify that
(a)
such assessment regarding capacity was carried
out and the assessment was properly documented;
(b)
the appearer possessed mental capacity at that
time; and
(c) the directive reflects the wishes of the appearer as
clearly expressed, during and after the discussion with the
medical practitioner.
(4)
The directive as prepared and certified in accordance with
this Act shall be signed by the appearer and by the medical
practitioner.
(5)
The model form contained in the Schedule to this Act and
the guidelines which the Minister may from time to time prescribe by
means of regulations, may be used for the purposes of assisting
appearers and medical practitioners in the drawing up of a directive.
(6)
(a)
Notwithstanding any other provision of this Act, any
processing of special categories of personal data, as referred to in
Article 9(1) of Regulation (EU) 2016/679, shall be carried out solely
for the purposes of drawing up, registering, recognising and, or
implementing an advance medical directive, and shall be performed
by, or under the responsibility of a medical practitioner subject to
professional secrecy obligations.
(b)
Such processing shall be proportionate to the aim pursued,
respect the essence of the right to data protection and provide for
suitable and specific measures to protect the fundamental rights and
the interests of the data subject.
(1)
An advance medical directive drawn up and certified
in accordance with article 4 shall be made in writing and shall be
authenticated by a notary public in accordance with article 2(2)(d) of
the Notarial Profession and Notarial Archives Act.
(2)
For the purposes of authentication, the appearer shall
personally appear before the notary public not later than three (3)
months from the date of the directive as drawn up by the appearer and
certified by the medical practitioner. The notary shall
(a)
verify the identity of the appearer;
(b)
confirm in a secure manner, that the appearer
acknowledges and reaffirms that the contents of the directive
express his present and settled wishes; and
(c)
authenticate the signature of the appearer.
(3)
The notary public shall, within fifteen (15) working days
from the date of authentication, submit to the Director of the Public
Registry a note of the directive.
(4)
The appearer, or any person authorised by the appearer,
shall submit the authenticated directive to the Director General for
Health Care Services.
(5)
Upon receipt of an authenticated directive in terms of sub-
article (4), the Director General for Health Care Services, established
under the Health Act, in his capacity as data controller for the purposes
of Regulation (EU) 2016/679, shall ensure that the advance medical
directive is recorded and archived in the medical records of the
appearer in such manner as may be prescribed.
(6)
Any personal data processed by the Department for Health
Care Services through the Director General for Health Care Services
or by notaries public for the purposes of this Act shall fully comply
with the provisions of Regulation (EU) 2016/679 of the European
Parliament and of the Council of 27 April 2016 on the protection of
natural persons with regard to the processing of personal data and on
the free movement of such data, and repealing Directive 95/46/EC (the
General Data Protection Regulation), and with the Data Protection
Act, including any regulations made thereunder, as well as with the
fundamental rights and freedoms of data subjects.
(7)
An advance medical directive shall be valid and have legal
effect from the moment of its authentication before a notary public,
notwithstanding that any registration or transmission in terms of this
Act has not yet taken place.
(1)
A directive shall form part of the confidential
medical records of the appearer and shall be stored in accordance with
industry standards and subject to the implementation of appropriate
technical and organisational measures to ensure a level of security
appropriate to the risks arising from the processing of personal data.
(2)
Access to a directive may be granted exclusively to a
medical practitioner subject to professional secrecy obligations who is
directly involved in the treatment of the appearer, and where such
access is strictly required for the provision of such treatment.
(1)
A directive shall be valid unless and until it is
revoked, amended or substituted in accordance with this Act.
(2)
A directive shall not have legal effect and shall not apply
where at the material time
(a)
the appearer has capacity to consent to or refuses
the treatment in question; or
(b)
the treatment or circumstances do not correspond
to those specified in the directive.
(3)
An appearer may revoke or amend a directive at any time
while having the required capacity.
(4)
Any revocation or amendment made orally in the presence
of a medical practitioner and at least one (1) witness shall be valid and
shall be documented by the medical practitioner in the medical records
of the appearer, subject to the obligations of the Director General for
Health Care Services under article 5(5).
(5)
Without prejudice to sub-article (4), any revocation or
amendment of a directive shall be made by a written declaration
authenticated before a notary and carried out in accordance with the
procedure applicable to a directive under article 5 of this Act.
PART III
Duties and Enforcement
(1)
Medical practitioners shall respect and give effect to
any valid and applicable directives.
(2)
Medical practitioners shall not incur any civil or criminal
liability for acting in accordance with a valid and applicable directive.
(3)
Where reasonable doubt arises as to the existence, validity
or applicability of a directive, any necessary treatment to prevent
serious and imminent deterioration of the appearer’s condition shall be
provided pending clarification or a decision by the competent court.
(4)
Any question as to the existence, validity or applicability of
a directive shall be determined by the Civil Court (Voluntary
Jurisdiction Section).
(5)
Any proceedings in accordance with this Act shall be
initiated by an application filed in the said Court as mentioned in sub-
article (4), which shall be determined within a period not exceeding
ten (10) days from the date of its filing in the registry of the court. The
Court may, where it considers appropriate, appoint one (1) or more
experts to assist it in its decision.
Any person who knowingly interferes with, falsifies,
conceals, or destroys a directive shall be guilty of an offence and shall
be liable on conviction to imprisonment for a term not exceeding
twelve (12) months, or to a fine (multa) not exceeding ten thousand
euro (€10,000), or to both such imprisonment and fine.
(1)
Any document or declaration made prior to the
coming into force of this Act, purporting to express the will of a
person concerning future medical treatment, shall not have legal effect
and shall not constitute a valid directive unless such wishes are
expressed anew in accordance with this Act
(2)
This article shall not invalidate or otherwise affect the legal
or clinical effect of any do-not-resuscitate (DNR) order or similar
treatment limitation issued by a medical practitioner in the course of a
patient’s care, where such order
(a)
was made following a contemporaneous
assessment of the patient’s clinical condition and
capacity; and
(b)
was recorded in the medical records of
such patient.
(1)
The Notarial Profession and Notarial Archives Act
shall be amended as follows
(i)
in paragraph (p) of sub-article (1) of article 50
thereof the word "Succession." shall be substituted by the word
"Succession;" and immediately thereafter there shall be added
the following new paragraph
"(q) any advance medical directive authenticated by a
notary in accordance with the Advance Medical Directives
Act.";
(ii)
sub-article (3) of article 50 thereof shall be
substituted by the following new sub-article
"(3) In the case of public wills or of the publication of
secret wills, or of advance medical directives authenticated in
accordance with the Advance Medical Directives Act, the note
shall only contain the date and nature of the act, and the
designation of the testator or appearer, as the case may be, in
accordance with article 28(1)(c).".
(2)
Sub-article (2) of article 8 of the Public Registry Act shall
be substituted by the following new sub-article
"(2)
In the case of a will, or of an advance medical directive
made and authenticated in accordance with the Advance Medical
Directives Act, the note shall only contain the date and nature of the act
and the designation of the testator or appearer, as the case may be, in
accordance with article 2042 of the Civil Code.".