use of gpp3 for ethical guidance – pubrica
DESCRIPTION
The following are some of the latest subjects discussed in GPP3: • The most recent ICMJE authorship conditions are explained (2013) • Authorship problems that are frequently found • Author payment and repayment are now more explicitly described. • Clarification of the words "ghost fiction" and "guest authorship." • Professional medical writers: what they do and how they help Continue Reading: https://bit.ly/2OOiUNI Reference: https://pubrica.com/services/publication-support/ Why Pubrica: When you order our services, We promise you the following – Plagiarism free | always on Time | 24*7 customer support | Written to international Standard | Unlimited Revisions support | Medical writing Expert | Publication Support | Biostatistical experts | High-quality Subject Matter Experts. Contact us : Web: https://pubrica.com/ Blog: https://pubrica.com/academy/ Email: [email protected] WhatsApp : +91 9884350006 United Kingdom: +44- 74248 10299TRANSCRIPT
Copyright © 2021 pubrica. All rights reserved 1
Use of GPP3 for Ethical Guidance
Dr. Nancy Agnes, Head,
Technical Operations, Pubrica
In-Brief
GPP3 is a revision of the original Good
Publication Practice (GPP) standards,
which were first published in 2003 and last
revised in 2009. The ISMPP GPP3
Steering Committee has revised the 2009
edition of the Good Publication Practice
Guidelines (GPP2) to emphasise integrity
and transparency in industry-sponsored
publication planning and development in
today's environment.
I. INTRODUCTION
GPP3 is a revised version of the Good
Publishing Practice (GPP) guideline that
offers guidelines for persons and
organisations involved in disseminating
research findings funded or assisted by
pharmaceutical, medical device, diagnostics,
and biotechnology industries. The guidelines
are meant to help individuals and
organisations adhere to legal and regulatory
standards while ensuring fair and open
publishing activities. These guidelines apply
to peer-reviewed journal publications and
oral and poster presentations at science
conferences.
The following are some of the latest subjects
discussed in GPP3:
The most recent ICMJE authorship
conditions are explained (2013)
Authorship problems that are frequently
found
Author payment and repayment are now
more explicitly described.
Clarification of the words "ghost fiction"
and "guest authorship."
Professional medical writers: what they
do and how they help
Advice on how to exchange data
acceptably.
II. GPP HISTORICAL ARCHIVE
GPP2 Guidelines, 2009
International Society for Medical
Publication Professionals (ISMPP)
assembled a Steering Committee to produce
an updated Good Publication Practice guide,
now known as "GPP2," to discuss
regulatory, guidance, and ethical changes
since 2003 and to affirm the goals of the
initial 2003 publication(4)
.
GPP Guidelines, 2003
The critical Good Publication Practice
(GPP) guidelines, released in 2003, aimed to
ensure that "clinical trials funded by
pharmaceutical firms are published
responsibly and ethically."
GPP3 for ethical guidelines, 2015
The resulting guideline adds new parts
(Principles of Good Publication Practice for
Company-Sponsored Medical Research,
Data Sharing, Studies That Should Be
Published, and Plagiarism). It builds on
Copyright © 2021 pubrica. All rights reserved 2
authorship requirements and widespread
authorship concerns established by the
International Committee of Medical Journal
Editors., Expand details on the position of
medical writers and explain appropriate
author payment and reimbursement.
Individuals and organisations can embody
honesty, transparency, and obligation for
reliable, complete, and transparent reporting
in their publications and presentations by
adopting good publishing practices
(including GPP3).
III. WHAT IS NEW IN GPP3
Guidance on updated ICMJE 2013
authorship criteria
Advice on everyday issues about
a uthors hip
Author payment and compensation
guidance and clarification
Further definitions of what creates
guest or ghost invention
Information on the position and
benefits of licenced medical authors
has been expanded
Advice for appropriate data sharing
Overall simplification of language
and format with a new guiding
principles section and quick reference
tables addressing guidance on
authorship criteria and joint authorship
issues
We use the terms "publications" and
"presentations" interchangeably in the
guideline to refer to the wide variety of
formats presented in peer-reviewed journals
(for example, original research papers, brief
reports, analyses, or letters to the editor) and
"abstracts," "posters," and slides for oral
presentations at scientific congresses.
"Sponsors" are organisations that offer
primary resources for a study, such as
funding. Professional medical researchers,
publishing designers, and publication
administrators are known as "publication
practitioners," and they work in or with
businesses. Regulatory documents, medical
education services, and marketing and
promotional materials are governed or
accredited by various national or state
bodies and are not protected by this
guideline.
IV. ROLE OF ISMPP
ISMPP was the energetic force behind the
adoption of the GPP3 guideline. By
supplying logistical research paper support,
giving access to the mailing list of ISMPP
participants, sending out e-mails to members
Copyright © 2021 pubrica. All rights reserved 3
and prospective reviewers, maintaining the
database of respondents, setting up the
reviewer Web site, and reviewing the GPP3
steering committee, the sponsor was able to
assist in the formation of the GPP3 steering
committee. Several members of the steering
committee also sit on the ISMPP Board of
Trustees. They did, however, contribute to
GPP3 as entities, not on behalf of ISMPP.
The quality of this guideline was not guided
or regulated by the ISMPP employees.
V. FUTURE SCOPES
We hope that GPP3 will add to the many
valuable guidelines and recommendations
that are already available (such as those
from the American Medical Writers
Association, Council of Science Editors,
Committee on Publication Ethics, European
Association of Science Editors, European
Medical Writers Association, ICMJE,
International Federation of Pharmaceutical
Manufacturers & Associations), ISMPP,
Medical Publishing Insights and Practices,
and the World Association of Medical
Editors) all promote responsible publishing
practices and research.
VI. CONCLUSION
Because of advancements in regulatory,
medical, and journal standards, our
understanding of the publishing environment
has changed. The GPP3 guideline has been
amended to keep up with the changes. The
role, reimbursements, and increased
responsibility of MWs in the process have
been identified and elaborated to a greater
extent. Necessitates MW staying current
with current trends and undergoing
specialised training from known institutions
to improve understanding and formulate a
proper strategy. It is required to produce
high-quality documentation and the bridging
of the gap between research conduct and
reporting. Avail Publication support services
from Pubrica.
REFERENCES
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Carswell CI, et al. Good Publication Practice for
Communicating Company-Sponsored Medical
Research: GPP3. Ann Intern Med. 2015;163:461-464;
doi:10.7326/M15-0288
2. Glasziou P, Altman DG, Bossuyt P, Boutron I, Clarke
M, Julious S, et al. Reducing waste from incomplete
or unusable reports of biomedical research. Lancet.
2014;383:267-76. [PMID: 24411647] doi:
10.1016/S0140-6736(13)62228-X
3. Wager E, Field EA, Grossman L. Good publication
practice for pharmaceutical companies. Curr Med Res
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4. Graf C, Battisti WP, Bridges D, Bruce-Winkler V,
Conaty JM, Ellison JM, et al; International Society for
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& Reporting. Good publication practice for
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19946142] doi:10.1136 /bmj.b4330
5. Wager E, Woolley K, Adshead V, Cairns A, Fullam J,
Gonzalez J, et al. Awareness and enforcement of
guidelines for publishing industry-sponsored medical
research among publication professionals: the Global
Publication Survey. BMJ Open. 2014;4:e004780.
[PMID: 24747794] doi:10.1136/bmjopen-2013-
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