Use of GPP3 for ethical guidance – Pubrica

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. 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.

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." (3)

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 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.

What is new in GPP3?

• Guidance on updated ICMJE 2013 authorship criteria
• Advice on everyday issues about authorship
• 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

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.

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 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.

Future Directions

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(5).

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.

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