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The European Register
for Specialists in Clinical Chemistry
and Laboratory Medicine: Code of Conduct
This article was published in: Clin Chem Lab
Med 2009;47(3):372-375
Version 2/ 2008
Approved by the EC4 Register Commission
and by the EFCC Executive Board in Paris on 6 November 2008 Abstract
In 1997, the European Communities
Confederation of Clinical Chemistry and Laboratory Medicine (EC4) set
up a Register for European Specialists in Clinical Chemistry and Laboratory
Medicine. The operation of the Register is undertaken by a Register Commission
(EC4RC). During the last 10 years more than 2000 specialists in clinical
chemistry and laboratory medicine have joined the Register. In 2007 EC4
merged with the Federation of European Societies of Clinical Chemistry
and Laboratory Medicine (FESCC) to form the European Federation of Clinical
Chemistry and Laboratory Medicine (EFCC). A Code of Conduct was adopted
in 2003
and a revised and updated version, taking account particularly of the
guidelines of the Conseil Européen des Professions Libérales
(CEPLIS) of which EFCC is a member, is presented in this article.
The
revised version was approved by the EC4 Register Commission and by
the EFCC Executive Board in Paris on 6 November 2008.
Introduction
Following the expansion of the European Union to 27 countries, and thus
the decreased geographical differences between the two organisations,
the European Communities Confederation of Clinical Chemistry and Laboratory
Medicine (EC4) merged with the Federation of European Societies of Clinical
Chemistry and Laboratory Medicine (FESCC) in 2007 to form the European
Federation of Clinical Chemistry and Laboratory Medicine (EFCC). EFCC
is now the European branch of IFCC. EC4 remains as a sub-section of EFCC
with responsibility for the operation of the EC4 Register of Specialists
in Clinical Chemistry and Laboratory Medicine.
One of the primary goals of EC4 and EFCC is to stimulate the professional
development of the Specialist in Clinical Chemistry and Laboratory Medicine
and the maintenance of his* professional activities at a very high level
(1,2). To further this aim, in 1998 EC4 set up the European registration
system, in which Specialists in Clinical Chemistry and Laboratory Medicine
of all countries affiliated to EC4 can be registered (3-5). One of the
conditions for registration is that the Specialist in Clinical Chemistry
and Laboratory Medicine undertakes to comply with the EC4 Code of Conduct
(5). This Code of Conduct is additional to and does not replace any Code
of Conduct to which the registrant might be subject to in his own country.
The original Code of Conduct was adopted in
2003 (6) and this has now been revised and updated taking account of
general changes in the field,
and particularly of the statement on common values adopted in 2007 by
CEPLIS (Conseil Européen des Professions Libérales, European
Council of the Liberal Professions) (7), of which EFCC is a member.
EC4/EFCC Code of Conduct
General principles
EFCC is the European professional organisation representing Specialists
in Clinical Chemistry and Laboratory Medicine, a profession determined
by its high level of professional qualifications. The relevant national
professional society in each of the EU Member States is represented within
EFCC.
In all their work, Specialists in Clinical Chemistry and Laboratory
Medicine shall conduct themselves in a manner that does not bring into
disrepute the discipline and the profession of Clinical Chemistry and
Laboratory Medicine. They shall value integrity, impartiality and respect
for persons and evidence and shall seek to establish the highest standards
of quality and ethics in their work. Because of their concern for valid
evidence, they shall ensure that research is carried out in keeping with
the highest standards of scientific integrity. Taking account of their
obligations under the law, they shall hold the interest and welfare of
patients and those in receipt of their services to be paramount at all
times and ensure that the interests of participants in research are safeguarded.
All registrants, having signed an application form, agree to abide by
this Code of Conduct. They are also obliged to comply with the Codes
of Conduct of their appropriate national registration body and national
societies, where appropriate.
Key principles
1. Quality and excellence
The Specialist in Clinical Chemistry and Laboratory Medicine shall put
his* knowledge and ability concerning laboratory diagnostics (including
the indication for analyses, the reliability of the results, the interpretation
of results and scientific research) at the service of diagnosis, therapy
and prevention of human and animal diseases. At all times he shall act
in the best interests of patients, subject to any over-riding legal requirements,
with the highest standards of competency and integrity.
2. Continuous professional development
In order to optimally fulfil his duties and in accordance with what
is regarded as good practice in his profession and having regard to the
laws of the country in which he is working, the Specialist in Clinical
Chemistry and Laboratory Medicine shall:
- maintain and develop his competence at the highest level of quality
by following all relevant (scientific and practical) developments concerning
health care in general and Clinical Chemistry and Laboratory Medicine
in particular, by participating in relevant training courses and other
appropriate continuous professional development programmes throughout
his working life, and by practising his profession on a regular basis;
- accept assignments only within his area of competence; beyond this
limit, he will seek the collaboration of appropriate experts;
- keep up-to-date with statutory codes of practice which affect
his work.
The Specialist in Clinical Chemistry and Laboratory Medicine
will display his commitment to the profession of Clinical Chemistry
and Laboratory
Medicine by taking part in the activities of its scientific
societies, notably those which promote the profession, and
contribute to
continuing training of their members.
3. Compliance with codes of ethics and conduct
The Specialist in Clinical Chemistry and Laboratory Medicine shall comply
not only with the provisions of this Code of Conduct but also with legislation
and with any codes of practice and standards relating to his professional
work which are applicable in the country in which he is working.
4. Honesty and integrity
The professional integrity and intellectual honesty of the Specialist
in Clinical Chemistry and Laboratory Medicine shall be the guarantee
of his impartiality of analysis, judgment and consequent decisions.
The Specialist in Clinical Chemistry and Laboratory Medicine shall at
all times avoid deceit in professional and scientific respect, such as
fraud, plagiarism, concealment, improper omission of information, and
expressing incorrect or misleading opinions in both clinical work and
in research.
The Specialist in Clinical Chemistry and Laboratory Medicine will not
accept any obligation that brings him into conflict with his professional
independence. In particular he undertakes:
- not to solicit for, or accept, gifts, pecuniary advantages or
benefits from the medical product or diagnostics industry, unless
they are of
low monetary value and relevant to the practice of Clinical
Chemistry and Laboratory Medicine;
- not to solicit for, or accept, hospitality at sales promotions,
symposia or congresses and the like unless this hospitality is
reasonable
in level and secondary to the main purpose of the meeting and
does not extend
to persons other than health professional;
- not to accept financial support from the industry, directly
or indirectly, other than for events for purely professional
and scientific purposes;
such gifts must always be reasonable in level and remain
subordinate to the main scientific objective of the event and
must not
be extended to persons other than health professionals.
5. Relationship with others
The Specialist in Clinical Chemistry and Laboratory Medicine shall at
all times act with courtesy, honest and integrity in his relationships
with patients and others, including professional colleagues, and must
not engage in any activity or behaviour which would bring the profession
into disrepute or undermine public confidence in the profession.
He must work constructively within a team, and communicate and co-operate
with other health professionals and others caring for patients.
He must not abuse his professional position to establish improper
relationships with patients, to persuade patients to give or lend
money or benefits,
to recommend treatments or investigations which are not in the patient’s
best interests, or to withhold investigations or treatments.
He must report concerns to employers or regulatory bodies where he
believes a colleague’s health, conduct or performance is a
threat to a patient.
6. Independence and impartiality
The Specialist in Clinical Chemistry and Laboratory Medicine must exercise
his professional judgment within the framework of his responsibilities
impartially and objectively, after taking into account all relevant circumstances,
in the best interests of his patient without pressure from external sources
or conflicts of interest. He will ensure that the interests of participants
in research are safeguarded and are paramount.
The Specialist in Clinical Chemistry and Laboratory Medicine will serve
the individual patient to the best of his ability and provide the general
public with such information, within in his field of competence, to enable
a proper understanding of health care matters of public interest.
8. Confidentiality
Without prejudice to legislation on privacy applicable in the country
where he is working, the Specialist in Clinical Chemistry and Laboratory
Medicine will consider himself bound to respect the confidentiality of
information obtained by him in his professional work. The Specialist
in Clinical Chemistry and Laboratory Medicine will be on his guard against
misuse of such information. He will ensure that information about a patient
or other individual is not disclosed to others except in specified circumstances,
such as to other health professionals involved in the care of the patient,
and, where possible, with the informed consent of the patient.
9. Conflict with moral and ethical beliefs
The Specialist in Clinical Chemistry and Laboratory Medicine is not
obliged to offer to provide a professional service in ways which conflict
with his own moral or religious beliefs, but must respect the moral,
religious and cultural beliefs of individual patients. He has an obligation
to provide information on where the service requested can most conveniently
be obtained from a professional colleague, or details of the institution
or professional organisation from which that information can be obtained.
If he has agreed to provide a service, he must set aside any personal
religious, cultural, philosophical or other convictions. He must ensure
equitable access to his services to all who are entitled to use them.
10. Delegation and supervision
As head and/or member of the team operating in the Clinical Chemistry
and Laboratory Medicine laboratory, the Specialist in Clinical Chemistry
and Laboratory Medicine will, given the specific circumstances of the
situation concerned:
- obtain a clear definition of the services required of him and/or
his team;
- ensure that all activities in the laboratory are organised and
executed as accurately and as quickly as possible;
- protect the safety and well-being of his colleagues and be
conscious of nature and the environment;
- show respect for superiors, colleagues and subordinates
by taking due account of their requirements and aspirations,
provided they conform
to the laws and ethics of their profession;
- strive for a high level of technical achievement which
will also contribute to and promote a healthy
and agreeable environment
for his colleagues;
- ensure that any member of support staff to whom a
task is delegated has the knowledge, skills
and competencies necessary
to undertake that task
effectively and efficiently, and that appropriate
supervision
is in place;
- retain responsibility for the task delegated,
except when the delegatee is at the same
level of professional
qualification.
11. Professional indemnity insurance
The Specialist in Clinical Chemistry and Laboratory Medicine should
have in place a form of insurance in respect of potential liabilities
to patients and, where applicable, to third parties arising out of his
professional work. This should be at a level sufficient to ensure that
a justified complainant would be adequately compensated. Such insurance
may be provided through a national arrangement for services provided
by the state, by an employer, through membership of a professional association
or by the individual practitioner. Exceptionally, and by formal prior
arrangement, the risk may be borne by the recipient of the service, in
Member States where legislation permits such an arrangement. The patient
should be made aware of these arrangements.
12. Advertising
Specialists in Clinical Chemistry and Laboratory
Medicine practise in both the public and private health sectors
and the relative distribution
between the two varies considerably between the Member States. In
Member States where advertising of a Specialist’s services is
permitted, any such advertising must be accurate, honest, legal, decent
and proportionate,
and must focus solely on the professional services offered. It must
also conform to any national or EU legislation and guidelines in this
area.
Sanctions Should a Specialist in Clinical Chemistry and Laboratory Medicine not
keep to a part of this Code of Conduct, his national regulatory body
(where applicable) and his national society will be responsible for determining
culpability and sanctions. However, if a registrant is subject to disciplinary
sanction (eg. suspension, removal) from their national register, EC4
will apply the same sanction to the individual in relation to the EC4
Register.
Transparency
The national professional societies are listed, with links, on the EC4
Register website (8) where there are also links to this Code of Conduct
and other documents. There are also links to the documents from the website
of the European Economic and Social Committee/Single Market Observatory
Self- and Co-regulation database (9). Public access to the names held
by the national regulatory bodies is available in some countries. At
present public access to the names of registrants on the EC4 Register
is not available but may be in the future. However this will require
consent from each individual.
*Throughout this document he/his are taken for he/she and his/her respectively
| By the EC4 Register Commission |
Gerard Sanders
|
Department of Clinical Chemistry,
Academic Medical Center, Amsterdam, The Netherlands
|
Matthias Opp
|
Laboratoire National de Sante, Luxembourg
|
Janet McMurray
|
Department of Clinical Biochemistry, Hope Hospital,
Salford, United Kingdom
|
Ursula Koeller
|
Institute for Medical and Chemical Laboratory
Diagnostics, Hospital Lainz, Vienna, Austria
|
Vic Blaton
|
Department of Clinical Chemistry, AZ Sint Jan
Hospitaal, Brugge, Belgium
|
Erik Lund
|
Department of Clinical Chemistry, Vejle County
Hospital, Vejle, Denmark
|
Aimo Harmoinen
|
TAYS, Laboratoriokeskus, Tampere, Finnland
|
| Simone Zerah |
Laboratoire d ’Analyses de Biologie Medicale, Bagnolet, Paris,
France |
| Hannsjoerg Baum |
Institut für Klinische Chemie und Pathobiochemie, Klinikum
rechts der Isar, Munich, Germany |
| Demetrios Rizos |
Hormone Laboratory, ‘‘Aretaieion’’ University
Hospital, Athens, Greece |
| Desmond Kenny |
Department of Clinical Biochemistry, Our Lady ’s Hospital
for Sick Children, Dublin, Ireland |
| Mario Pazzagli |
Department for Clinical Pathophysiology, University of Florence,
Florence, Italy |
| Hans Hoffman |
Department of Clinical Chemistry, Catharina Hospital, Eindhoven,
The Netherlands |
| Henrique Reguengo |
Servigo de Quimica Clinca, Hospital Geral de Santo Antonio, Porto,
Portugal |
| JoseM.Queralto |
Servicio de Bioquimica, Hospital de la Santa Creui Sant Pau, Barcelona,
Sain |
| Hans Wallinder |
Department of Clinical Chemistry, Medilab AB, Ta ¨by, Sweden |
| Rob Jansen |
Director SKML, UMC St. Radboud, Nijmegen, The
Netherlands |
| Michael Hallworth |
Department of Clinical Chemistry, RoyalShrewsbury Hospital, Shrewsbury,
United Kingdom |
| Peter Schuff-Werner |
Institute for Clinical Chemistry and Pathobiochemistry, University
of Rostock, Rostock, Germany |
| Corresponding author: Janet McMurray, EC4 Register
Commission, Department of Clinical Biochemistry, Hope Hospital, Salford
M6 8HD, United Kingdom Phone: +44-161-206-4955, Fax: +44-161-788-7443,
E-mail: janet.mcmurray@srht.nhs.uk |
| References |
Sanders GTB, Kelly AM,
Breuer J, Mocarelli P. |
The role of European
Communities Confederation of Clinical Chemistry (EC4) in the harmonisation
of clinical chemistry in the European Union (letter)
Eur J Clin Chem Clin Biochem 1995;33:947-948. |
Sanders GT, Jansen RT, Beastall G,
Gurr E, Kenny D, Kohse KP et al. |
Recent activities of EC4 in the harmonisation
of clinical chemistry in the European Union.
Clin Chem Lab Med 1999;37:477–480. |
Sanders GT, Kelly AM, Breuer J,
Kohse KP, Mocarelli P, Sachs C. |
The European Register for clinical
chemists.
Eur J Clin Chem Clin Biochem 1997;35:795-796. |
Sanders GT, Kelly AM, Breuer J,
Kohse KP, Mocarelli P, Sachs C. |
European Communities Confederation
of Clinical Chemistry
Guide to the EC4 Register: European clinical chemist
Eur J Clin Chem Clin Biochem 1997;35:797-803. |
Gurr E, Koeller U, Blaton V, Lund
E, Harmoinen S et al. |
The European Register for Specialists
Chemistry and Laboratory Medicine: Guide to the Version 2-2003
and Procedure for Re-registration.
Chem Lab Med 2003;41:238-247. |
| Sanders G, Opp M, McMurray J, Koeller U, Blaton V,
Lund E et al. |
The European Register for Specialists in Clinical Chemistry
and Laboratory Medicine: Code of Conduct. Clin Chem Lab Med 2004;
42: 563-565. |
| |
Conseil Européen des Professions Libérales.
Common Values of the Liberal Professions in the European Union; 2007. |
| |
European Economic and Social Committee, Single Market
Observatory Self- and Co-regulation Database. |
|