Therapeutic Advances in Drug Safety
Journal Highlights
- Launched in 2010.
- Gold open access journal – all articles are made freely available online immediately upon publication.
- Rigorous peer review.
- Listed in PubMed and indexed in Clarivate Analytics: Science Citation Index Expanded (SCIE), Scopus, and International Pharmaceutical Abstracts (ProQuest).
- Over 220,000 full article views annually.
Therapeutic Advances in Drug Safety is a peer-reviewed open access journal which focuses on pioneering efforts and innovative studies across all areas of drug safety. Please see the Aims and Scope tab for further information.
The journal is a member of the Committee on Publication Ethics (COPE).
Diversity, Equity and Inclusion Statement
Therapeutic Advances in Drug Safety (TADS) promotes inclusive, open science that reflects the disciplinary, human, and geographic diversity of the drug safety community.
Diversity as a core value embodies inclusiveness, mutual respect, and multiple perspectives.
We welcome editors, editorial board members, peer reviewers and authors from all backgrounds, cultures, ethnicities, nationalities, races, religions, sexes, sexual orientations, gender identities, mental or physical (dis)abilities, ages, career stages, socioeconomic status or any other individual status.
We are committed to continually improving our editorial and review processes whilst playing our part in eradicating bias and inequality in all forms.
Submission information
Submit your manuscript today at http://mc.manuscriptcentral.com/tads.
Please see the Submission Guidelines tab for more information on how to submit your article to the journal.
Open access information
The article processing charge (APC) for this journal is currently $3000 USD. The APC for a Plain Language Summary is $5000.
The APC is payable when a manuscript is accepted after peer review, before it is published. The APC is subject to taxes where applicable. Please see further details here.
Contact
Please direct any enquiries to tads@sagepub.co.uk.
This journal changed its publication mode from subscription to open access in 2019.
Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed open access original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in drug safety, providing an online forum for rapid dissemination of recent research and perspectives in this area.
The journal is dedicated to publishing clinical research, including qualitative studies. We do not publish preclinical research, including basic laboratory research and animal studies.
Review articles include expert opinion pieces, perspective reviews (including single-drug and drug class reviews), patient perspectives, narrative reviews and therapeutic area reviews. Systematic reviews, meta-analyses, postmarketing and health economic and pharmacoeconomic reviews are also welcomed. The appropriate EQUATOR Network reporting guidelines should be followed (e.g. CONSORT for randomized, controlled trials and PRISMA for systematic reviews/meta-analyses). The journal conforms to the ICMJE requirement that clinical trials are registered in a WHO-approved public trials registry at or before the time of first patient enrolment as a condition of consideration for publication. The trial registry name and URL, and registration number must be included at the end of the abstract.
The journal adheres to a blind review process in which the reviewer's name is routinely withheld from the author unless the reviewer requests a preference for their identity to be revealed. Manuscripts are reviewed by at least two referees.
| Arduino Mangoni MD, MRCP (UK), FRACP, FRCP (London), FRCP (Glasgow), FRCP (Edinburgh) | Flinders Medical Centre and Flinders University, Bedford Park, Australia |
| Shasha Sharief | SAGE Publishing, London, UK |
| Shikha Tomar | SAGE Publishing, India |
| Joris Berwaerts MD | J&J Pharmaceutical Research & Development, USA |
| Samantha Lane, MSc | Drug Safety Research Unit, Southampton, UK |
| Roy Soiza MB, ChB. MRCP | NHS Grampian, Aberdeen, UK |
| Stephen Waring BMedSci, MB, BCh, BAO, PhD | York Hospitals NHS Trust, UK |
| Royes Joseph, PhD | School of Medicine, Keele University, UK |
| Chang-Xing Ma, PhD | Department of Biostatistics, University at Buffalo, New York, USA |
| Mandy Michelle McBroom MPH | UT Southwestern Medical Center, USA |
| Yoshihiro Noguchi, PhD | Gifu Pharmaceutical University, Japan |
| Sameer Khan | SAGE Publishing, India |
| Sara Tommasi, PhD | Flinders University, Adelaide, Australia |
| Anna Birna Almarsdóttir PdD, MS, MSc | University of Copenhagen, Copenhagen, Denmark |
| Christopher Beer MB, BS, GradCertHPEd, PhD, FRACP | Royal Perth Hospital, Perth, WA, Australia |
| J Simon Bell PhD | Monash University, Melbourne, Australia |
| Phil Berry MBBS, Mphil | Independent Pharmaceutical Consultant, Geneva, Switzerland |
| Carlos-Alberto Calderon-Ospina MD, PhD, MSc | Pharmacology Unit, School of Medicine and Health Sciences, Universidad del Rosario, Bogota, Colombia |
| Kin-Wei Chan MD, ScD, FISPE | National Taiwan University, Taipei, Taiwan |
| Antonio Cherubini MD, PhD | IRCCS INRCA, Ancona, Italy |
| Bernard Cheung MA, MB BChir, PhD, MRCP, FRCP, FCP, FHKCP, FHKAM (Medicine) | The University of Hong Kong, Hong Kong |
| Claire Davies | Medicines and Healthcare Products Regulatory Agency, London, UK |
| Alex Dodoo B.Pharm, MSc, PhD, FPSGH, FPCPharm | University of Ghana Medical School, Accra, Ghana |
| Matthew P. Doogue BSc, MBCHB, DipPaed, FRACP | Univeristy of Otago Christchurch, New Zealand |
| Phil Hannaford MBChB | University of Aberdeen, Aberdeen, UK |
| Manfred Hauben MD, PhD | New York, NY, USA |
| Sarah Hilmer BScMed, MBBS, FRACP, PhD | Royal North Shore Hospital, St Leonards, NSW, Australia |
| Paul Jansen MD, PhD | University Medical Centre, Utrecht, Netherlands |
| Jimmy Jose MPharm, PhD | School of Pharmacy, University of Nizwa, Oman |
| Neil Kaplowitz MD | University of Southern California, Los Angeles, CA, USA |
| Star Khoza, PhD | University of the Western Cape, South Africa |
| Stephen Leslie BSc, MB ChB, PhD, FRCP | Raigmore Hospital, Inverness, UK |
| Sunny Linnebur Pharm.D, FCCO, BCPS, CGP | Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Denver, Colorado, USA |
| Mary J Macleod BSc, MBChB, PhD, FRCP | University of Aberdeen, Aberdeen, UK |
| Jennifer Martin MA, MBBS, PhD | University of Queensland, Brisbane, QLD, Australia |
| Glenn Matfin MB, ChB | National Health Service, London, UK |
| Patricia Mcgettigan MD, FRCPI, FRACP | Hull York Medical School, Hull/York, UK |
| Christoph Meier PhD, MSc | University Hospital Basel, Basel, Switzerland |
| Tadele Mekuriya Yadesa, B.Pharm, MSc, Ph.D | Kampala International University, Uganda |
| Yola Moride PhD, FISPE | Rutgers University, New Jersey, USA |
| Vicky Parikh MD, PPH | Mid-Atlantic Medical Research Centers, Hollywood, MD, USA |
| Emilio Perucca | University of Pavia, Pavia, Italy |
| Philip Pierce MD | Johnson & Johnson Pharmaceutical Research and Development, Titusville, NJ, USA |
| Munir Pirmohamed BChB, MRCO, PhD, FRCP, FBPharmacolS | University of Liverpool, Liverpool, UK |
| Thomas M. Polasek BSc, BPharm, PhD | Flinders University, Adelaide, SA, Australia |
| Elena Ramírez, PhD, MD | Autonomous University of Madrid, Spain |
| Amrit Ray MD, MBA | Johnson & Johnson Pharmaceuticals Group, Titusville, NJ, USA |
| Michael Rieder MD, PhD | Childrens Hospital of W. Ontario, London, ON, Canada |
| Luis Rios-Nogales MD, PhD | Rational Vaccines, Boston, MA, USA |
| Greg Roberts Bpharm | Repatriation General Hospital, Daw Park, SA, Australia |
| Allen Root | University of South Florida, USA |
| Andrew Rowland | Flinders University, Australia |
| Debabrata Roy, PhD, MSc | Drug Safety Research Unit, Southampton, UK |
| Leo Russo MS, PhD | Shire Pharmaceuticals, Wayne, PA, USA |
| Mohammed Salahudeen BPharm, PharmD, MBA, PhD, AFHEA | School of Pharmacy and Pharmacology, University of Tasmania, Hobart, Australia |
| Gaetano Santulli, MD, PhD, FAHA | Albert Einstein College of Medicine, USA |
| Marco Sardella, PharmD, EEA QPPV | ADIENNE Pharma & Biotech, Monza e Brianza, Italy |
| Carmelo Scarpignato MD, DSc, FRCP, FACP, FACG | University of Parma, Parma, Italy |
| Rashmi Shah BSc, MBBS, FRCP, FRCP, MD, FFPM, HonFBPhS | Rashmi Shah Consultancy Ltd, Gerrards Cross, UK |
| Michael Sorich | Flinders University, Australia |
| Scott Twaddell BMedSc, BMed, GCClinTox, FRACP | University of Newcastle, Newcastle, NSW, Australia |
| Allen Vaida PharmD, BSc | Institute of Safe Medication Practices, Horsham, PA, USA |
| Tjeerd Van Staa MD, PhD, MA, MSc | Medicines and Healthcare Products Regulatory Agency, London, UK |
| David Williams PhD, FRCP | Royal College of Surgeons, Eire, Ireland |
| Richard Woodman PhD, MBiostats, MMedSco, BSc | Flinders University, Bedford Park, Australia |
| Jane Woolley PhD | Medicines and Healthcare products Regulatory Agency, USA |
| Jian Zhang, PhD | Zhujiang Hospital of Southern Medical University, China |
| Tina Aswani Omprakash | Patient Advocate |
| Trishna Bharadia | Patient Advocate, Maidenhead, UK |
| Anisha Gangotra | Patient Advocate, High Wycombe, UK |
| Dominique Hamerlijnck MPhil, MBA | European Patients' Academy (EUPATI), Amsterdam, Netherlands |
| Sheila Khawaja | The World Alliance of Pituitary Organizations (WAPO), Monfalcone, Italy |
| Paola Kruger | European Patients' Academy (EUPATI), Rome, Italy |
| Oisín Kavanagh, MPharm, MPSI, MPSNI, PhD | Newcastle University, United Kingdom |
| Olivia Lounsbury, BS | Johns Hopkins Hospital, Baltimore, MD, USA |
| Sule Ajibola Saka, BPharm; MPharm; PhD, UKZN | Faculty of Pharmacy, Olabisi Onabanjo University, Agoiwoye, Nigeria |
| Vasileios-Periklis Stamatellos, MD, MSc | Aristotle University of Thessaloniki, Department of Clinical Pharmacology, Greece |
| Nuru Abdu, BPharm | Department of Medical Services, Ministry of Health, Asmara, Eritrea |
| May Almukainzi, PhD | Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia |
| Mukhtar Ansari, PhD | University of Ha'il, Hail, Saudi Arabia |
| Tesfay Mehari Atey, PhD, MBA, MSc, BPharm | Department of Clinical Pharmacy, School of Pharmacy, College of Health Sciences, Mekelle University School of Pharmacy and Pharmacology, College of Health and Medicine, University of Tasmania |
| Kimberly L. Barefield, PharmD, MHA, CDCES, BCPS | Philadelphia College of Osteopathic Medicine, Georgia, USA |
| Patrick E. Beeler, MD | University of Lucerne, Switzerland |
| Jaden Brandt, BSc.Pharm, MSc, DipPH | University of Manitoba, Manitoba, Canada |
| Franco WT CHENG, PhD, MClinPharm, BPharm | University of Hong Kong, Hong Kong, China |
| Rakesh Dixit, MD | Pharmacology and Therapeutics King George's Medical University Lucknow, Uttar Pradesh, India |
| Sherif Eltonsy, PhD | University of Manitoba, Canada |
| Jaqueline Eserian, PhD | Adolfo Lutz Institute, São Paulo, Brazil |
| Ioana Frent, MD, PhD | ICON Plc, Romania |
| Jennifer Ilomaki, Msc, MD | Centre for Medicine Use and Safety, Monash University, Australia |
| Noami Jessurun, PharmD, PhD | Pharmacovigilance Centre Lareb, The Netherlands |
| Mahmathi Karuppannan, BPharm (Hons.), MPharm, Ph.D | Universiti Teknologi MARA, Shah Alam Selangor, Malaysia |
| Ronald Kiguba, BPharm, MSc, PhD | Makerere University College of Health Sciences, Uganda |
| Syed Arman Rabbani, PhD | RAK Medical & Health Sciences University, UAE |
| Alice Ramos-Silva, PharmD, PhD | Department of Drugs and Medicines (DEFARMED), Federal University of Rio de Janeiro, Rio de Janeiro, Brazil |
| Daniela A. Rodrigues, MSc | Research Laboratory on Epidemiology and Population Health, Polytechnic of Guarda, Portugal |
| Maha Saad, PharmD, BCGP, BCPS | St. John's University College of Pharmacy and Health Sciences, US |
| Jyotirmoy Sarker, MPharm, MBiotech, MBA | University Of Illinois Chicago, Chicago, IL, USA |
| Ratree Sawangjit, B. Pharm, PhD | Mahasarakham University Kamrieng, Kantarawichai, Mahasarakham, Thailand |
| Leticia A. Shea, PharmD, BCACP | Regis University, USA |
| Siti Maisharah Sheikh Ghadzi, PhD | Universiti Sains Malaysia, Malaysia |
| Hege Sletvold, Cand.pharm., PhD | Nord University, Norway |
| Francisco Somoza-Cano, MD | Cleveland Clinic Union Hospital, USA |
| Carrie Stewart, PhD | Institute of Applied Health Sciences, University of Aberdeen, Scotland |
| Selvarani Subbarayan, MBBS, MSc., PhD | Novabiotics, UK |
| Mojtaba Vaismoradi, Prof., PhD, MScN, BScN | Nord University, Bodø, Norway |
| Lorenzo Villa-Zapata, PharmD, PhD | University of Georgia College of Pharmacy, USA |
| Chen-Yu Wang, PhD | National Center for Geriatric and Welfare Research, National Health Research Institutes, Miaoli County, Taiwan |
| Liknaw Workie Limenh, MSc | University of Gondar, Gondar, Ethiopia |
| Andrew Y. Hwang ,PharmD, BCPS | Massachusetts College of Pharmacy and Health Sciences, Boston, MA, USA |
| Nadir Yalcin, PhD | Hacettepe University, Ankara, Turkey |
Manuscript Submission Guidelines: Therapeutic Advances in Drug Safety
This Journal is a member of the Committee on Publication Ethics.
This Journal recommends that authors follow the Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly Work in Medical Journals formulated by the International Committee of Medical Journal Editors (ICMJE).
All articles are listed on PubMed.
Please read the guidelines below then visit the Journal’s submission site http://mc.manuscriptcentral.com/tads to upload your manuscript. Please note that manuscripts not conforming to these guidelines may be returned.
Only manuscripts of sufficient quality that meet the aims and scope of Therapeutic Advances in Drug Safety will be reviewed.
There are no fees payable to submit or publish in this journal.
As part of the submission process you will be required to warrant that you are submitting your original work, that you have the rights in the work, that you are submitting the work for first publication in the Journal and that it is not being considered for publication elsewhere and has not already been published elsewhere, and that you have obtained and can supply all necessary permissions for the reproduction of any copyright works not owned by you.
- What do we publish?
1.1 Aims & Scope
1.2 Article types
1.3 Writing your paper - Editorial policies
2.1 Peer review policy
2.2 Authorship
2.3 Acknowledgements
2.4 Funding
2.5 Declaration of conflicting interests
2.6 Research ethics and patient consent
2.7 Clinical trials
2.8 Reporting guidelines
2.9 Data - Publishing policies
3.1 Publication ethics
3.2 Contributor's publishing agreement
3.3 Open access and author archiving - Preparing your manuscript
4.1 Formatting
4.2 Artwork, figures and other graphics
4.3 Supplementary material
4.4 Reference style
4.5 English language editing services - Submitting your manuscript
5.1 ORCID
5.2 Information required for completing your submission
5.3 Permissions - On acceptance and publication
6.1 SAGE Production
6.2 Online First publication
6.3 Access to your published article
6.4 Promoting your article - Further information
Before submitting your manuscript to Therapeutic Advances in Drug Safety, please ensure you have read the Aims & Scope.
Therapeutic Advances in Drug Safety considers the following article types for publication:
- Original Articles. The Editors will consider preclinical, interventional and observational studies with clearly stated aims, well-reported methodology (including main outcome measures) and results, and a discussion of the results in the context of the published literature.
- Review Articles. These manuscripts are usually commissioned by the Editors, but the following types of high-quality review will be considered:
(a) General reviews that provide a synthesis of an area that fits within the aims and scope of the journal;
(b) Perspective reviews – review articles that address important new areas of general interest and afford the author the opportunity to present a forward-looking perspective on the topic;
(c) Drug reviews – review articles focusing on the available evidence for the use of a particular drug or combination therapy. - Systematic Reviews – these should answer a specific research question and be reported according to the PRISMA guidelines. They should also include a PRISMA flow chart as a cited figure and a completed PRISMA checklist as a supplementary file (please see section 2.8).
- Meta-analyses – these should answer a specific research question and be reported according to the PRISMA guidelines. They should also include a PRISMA flow chart as a cited figure and a completed PRISMA checklist as a supplementary file (please see section 2.8).
- Case Reports – these structured reports should describe an unusual case and include a full review of the pertinent literature and a section on implications for clinical care.
- Case Series – these descriptive structured reports (which do not involve formal hypotheses or pre-specified methodology or analyses) of a small group of patients should include a full review of the pertinent literature and a section on implications for clinical care.
- Study Protocols – these can be for forthcoming or ongoing research. Information on trial registration (where applicable) and ethics approval should be included in the manuscript.
- Letters to the Editor – these brief opinion pieces should be as concise as possible, usually no more than 1000 words.
The journal considers the results of rigorous, well-designed studies that demonstrate “no effect” or that fail to replicate previous work (“negative data”) as important to the advancement of science. Therapeutic Advances in Drug Safety welcomes short reports on null or negative results as long as the papers are based on strong hypothesis testing.
The SAGE Author Gateway has some general advice and on how to get published, plus links to further resources.
1.3.1 Make your article discoverable
When writing up your paper, think about how you can make it discoverable. The title, keywords and abstract are key to ensuring readers find your article through search engines such as Google. For information and guidance on how best to title your article, write your abstract and select your keywords, have a look at this page on the Gateway: How to Help Readers Find Your Article Online.
The journal's policy is to obtain at least two independent reviews of each article. Therapeutic Advances in Drug Safety operates a conventional single-blind reviewing policy in which the reviewer's name is always concealed from the submitting author. Referees will be encouraged to provide substantive, constructive reviews that provide suggestions for improving the work and distinguish between mandatory and non-mandatory recommendations. All manuscripts accepted for publication are subject to editing for presentation, style and grammar. Any major redrafting is agreed with the author but the Editor's decision on the text is final.
As part of the submission process you will be asked to provide the names of 3 peers who could be called upon to review your manuscript. Recommended reviewers should be experts in their fields and should be able to provide an objective assessment of the manuscript. Please be aware of any conflicts of interest when recommending reviewers. Examples of conflicts of interest include (but are not limited to) the below:
- The reviewer should have no prior knowledge of your submission
- The reviewer should not have recently collaborated with any of the authors
- Reviewer nominees from the same institution as any of the authors are not permitted
You will also be asked to nominate peers who you do not wish to review your manuscript (opposed reviewers).
Please note that the Editors are not obliged to invite/reject any recommended/opposed reviewers to assess your manuscript.
The Editor or members of the Editorial Board may occasionally submit their own manuscripts for possible publication in the journal. In these cases, the peer review process will be managed by alternative members of the Board and the submitting Editor/Board member will have no involvement in the decision-making process.
Papers should only be submitted for consideration once consent is given by all contributing authors. Those submitting papers should carefully check that all those whose work contributed to the paper are acknowledged as contributing authors.
The list of authors should include all those who can legitimately claim authorship. This is all those who:
- Made a substantial contribution to the concept or design of the work; or acquisition, analysis or interpretation of data,
- Drafted the article or revised it critically for important intellectual content,
- Approved the version to be published,
- Each author should have participated sufficiently in the work to take public responsibility for appropriate portions of the content.
Authors should meet the conditions of all of the points above. When a large, multicentre group has conducted the work, the group should identify the individuals who accept direct responsibility for the manuscript. These individuals should fully meet the criteria for authorship.
Acquisition of funding, collection of data, or general supervision of the research group alone does not constitute authorship, although all contributors who do not meet the criteria for authorship should be listed in the Acknowledgments section. Please refer to the International Committee of Medical Journal Editors (ICMJE) authorship guidelines for more information on authorship.
All contributors who do not meet the criteria for authorship should be listed in an Acknowledgements section. Examples of those who might be acknowledged include a person who provided purely technical help, or a department chair who provided only general support.
Any acknowledgements should appear first at the end of your article prior to your Declaration of Conflicting Interests (if applicable), any notes and your References.
2.3.1 Writing assistance
Individuals who provided writing assistance, e.g. from a specialist communications company, do not qualify as authors and so should be included in the Acknowledgements section. Authors must disclose any writing assistance – including the individual’s name, company and level of input – and identify the entity that paid for this assistance. It is not necessary to disclose use of language polishing services.
Therapeutic Advances in Drug Safety requires all authors to acknowledge their funding in a consistent fashion under a separate heading. Please visit the Funding Acknowledgements page on the SAGE Journal Author Gateway to confirm the format of the acknowledgment text in the event of funding, or state that: This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
2.5 Declaration of conflicting interests
It is the policy of Therapeutic Advances in Drug Safety to require a declaration of conflicting interests from all authors enabling a statement to be carried within the paginated pages of all published articles.
Please ensure that a ‘Declaration of Conflicting Interests’ statement is included at the end of your manuscript, after any acknowledgements and prior to the references. If no conflict exists, please state that ‘The Author(s) declare(s) that there is no conflict of interest’. For guidance on conflict of interest statements, please see the ICMJE recommendations here.
2.6 Research ethics and patient consent
Medical research involving human subjects must be conducted according to the World Medical Association Declaration of Helsinki.
Submitted manuscripts should conform to the ICMJE Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly Work in Medical Journals, and all papers reporting animal and/or human studies must state in the methods section that the relevant Ethics Committee or Institutional Review Board provided (or waived) approval. Please ensure that you have provided the full name and institution of the review committee, in addition to the approval number.
For research articles, authors are also required to state in the methods section whether participants provided informed consent and whether the consent was written or verbal.
Information on informed consent to report individual cases or case series should be included in the manuscript text. A statement is required regarding whether written informed consent for patient information and images to be published was provided by the patient(s) or a legally authorized representative.
Please also refer to the ICMJE Recommendations for the Protection of Research Participants.
All research involving animals submitted for publication must be approved by an ethics committee with oversight of the facility in which the studies were conducted. The journal has adopted the Consensus Author Guidelines on Animal Ethics and Welfare for Veterinary Journals published by the International Association of Veterinary Editors.
Therapeutic Advances in Drug Safety endorses the ICMJE requirement that clinical trials are registered in a WHO-approved public trials registry at or before the time of first patient enrolment. However, consistent with the AllTrials campaign, retrospectively registered trials will be considered if the justification for late registration is acceptable. The trial registry name and URL, and registration number must be included at the end of the abstract.
The relevant EQUATOR Network reporting guidelines should be followed depending on the type of study. For example, all randomized controlled trials submitted for publication should include a completed CONSORT flow chart as a cited figure and the completed CONSORT checklist should be uploaded with your submission as a supplementary file. Systematic reviews and meta-analyses should include the completed PRISMA flow chart as a cited figure and the completed PRISMA checklist should be uploaded with your submission as a supplementary file. The EQUATOR wizard can help you identify the appropriate guideline.
Other resources can be found at NLM’s Research Reporting Guidelines and Initiatives.
SAGE acknowledges the importance of research data availability as an integral part of the research and verification process for academic journal articles.
Therapeutic Advances in Drug Safety requests all authors submitting any primary data used in their research articles alongside their article submissions to be published in the online version of the journal, or provide detailed information in their articles on how the data can be obtained. This information should include links to third-party data repositories or detailed contact information for third-party data sources. Data available only on an author-maintained website will need to be loaded onto either the journal’s platform or a third-party platform to ensure continuing accessibility. Examples of data types include but are not limited to statistical data files, replication code, text files, audio files, images, videos, appendices, and additional charts and graphs necessary to understand the original research. The editor may consider limited embargoes on proprietary data. The editor can also grant exceptions for data that cannot legally or ethically be released. All data submitted should comply with Institutional or Ethical Review Board requirements and applicable government regulations. For further information, please contact the editorial office at tads@sagepub.co.uk
SAGE is committed to upholding the integrity of the academic record. We encourage authors to refer to the Committee on Publication Ethics’ International Standards for Authors and view the Publication Ethics page on the SAGE Author Gateway.
3.1.1 Plagiarism
Therapeutic Advances in Drug Safety and SAGE take issues of copyright infringement, plagiarism or other breaches of best practice in publication very seriously. We seek to protect the rights of our authors and we always investigate claims of plagiarism or misuse of published articles. Equally, we seek to protect the reputation of the journal against malpractice. Submitted articles may be checked with duplication-checking software. Where an article, for example, is found to have plagiarised other work or included third-party copyright material without permission or with insufficient acknowledgement, or where the authorship of the article is contested, we reserve the right to take action including, but not limited to: publishing an erratum or corrigendum (correction); retracting the article; taking up the matter with the head of department or dean of the author's institution and/or relevant academic bodies or societies; or taking appropriate legal action.
3.1.2 Prior publication
If material has been previously published it is not generally acceptable for publication in a SAGE journal. However, there are certain circumstances where previously published material can be considered for publication. Please refer to the guidance on the SAGE Author Gateway or if in doubt, contact the Editor at the address given below.
3.2 Contributor's publishing agreement
Before publication, SAGE requires the author as the rights holder to sign a Journal Contributor’s Publishing Agreement. SAGE’s Journal Contributor’s Publishing Agreement is an exclusive licence agreement which means that the author retains copyright in the work but grants SAGE the sole and exclusive right and licence to publish for the full legal term of copyright. Exceptions may exist where an assignment of copyright is required or preferred by a proprietor other than SAGE. In this case copyright in the work will be assigned from the author to the society. For more information please visit the SAGE Author Gateway.
3.3 Open access and author archiving
Therapeutic Advances in Drug Safety offers optional open access publishing via the SAGE Choice programme. For more information please visit the SAGE Choice website. For information on funding body compliance, and depositing your article in repositories, please visit SAGE Publishing Policies on our Journal Author Gateway.
4. Preparing your manuscript for submission
The preferred format for your manuscript is Word. LaTeX files are also accepted. Word and LaTex templates are available on the Manuscript Submission Guidelines page of our Author Gateway.
4.2 Artwork, figures and other graphics
For guidance on the preparation of illustrations, pictures and graphs in electronic format, please visit SAGE’s Manuscript Submission Guidelines.
This journal is able to host additional materials online (e.g. datasets, podcasts, videos, images etc) alongside the full-text of the article. For more information please refer to our guidelines on submitting supplementary files.
Therapeutic Advances in Drug Safety adheres to the SAGE Vancouver reference style. View the SAGE Vancouver guidelines to ensure your manuscript conforms to this reference style.
If you use EndNote or Zotero to manage references, you can download the appropriate output style file to help format your references quickly.
4.5 English language editing services
Authors seeking assistance with English language editing, translation, or figure and manuscript formatting to fit the journal’s specifications should consider using SAGE Language Services. Visit SAGE Language Services on our Journal Author Gateway for further information.
Therapeutic Advances in Drug Safety is hosted on SAGE Track, a web based online submission and peer review system powered by ScholarOne™ Manuscripts. Visit http://mc.manuscriptcentral.com/tads to login and submit your article online.
IMPORTANT: Please check whether you already have an account in the system before trying to create a new one. If you have reviewed or authored for the journal in the past year it is likely that you will have had an account created. For further guidance on submitting your manuscript online please visit ScholarOne Online Help.
As part of our commitment to ensuring an ethical, transparent and fair peer review process SAGE is a supporting member of ORCID, the Open Researcher and Contributor ID. ORCID provides a persistent digital identifier that distinguishes researchers from every other researcher and, through integration in key research workflows such as manuscript and grant submission, supports automated linkages between researchers and their professional activities ensuring that their work is recognised.
We encourage all authors to add their ORCIDs to their SAGE Track accounts and include their ORCIDs as part of the submission process. If you don’t already have one you can create one here.
5.2 Information required for completing your submission
You will be asked to provide contact details and academic affiliations for all co-authors via the submission system and identify who is to be the corresponding author. These details must match what appears on your manuscript. At this stage please ensure you have included all the required statements and declarations and uploaded any additional supplementary files (including reporting guidelines where relevant).
Please also ensure that you have obtained any necessary permission from copyright holders for reproducing any illustrations, tables, figures or lengthy quotations previously published elsewhere. For further information including guidance on fair dealing for criticism and review, please see the Copyright and Permissions page on the SAGE Author Gateway.
6. On acceptance and publication
Your SAGE Production Editor will keep you informed as to your article’s progress throughout the production process. Proofs will be sent by PDF to the corresponding author and should be returned promptly. Authors are reminded to check their proofs carefully to confirm that all author information, including names, affiliations, sequence and contact details are correct, and that Funding and Conflict of Interest statements, if any, are accurate. Please note that if there are any changes to the author list at this stage all authors will be required to complete and sign a form authorising the change.
Online First allows final articles (completed and approved articles awaiting assignment to a future issue) to be published online prior to their inclusion in a journal issue, which significantly reduces the lead time between submission and publication. Visit the SAGE Journals help page for more details, including how to cite Online First articles.
6.3 Access to your published article
SAGE provides authors with online access to their final article.
Publication is not the end of the process! You can help disseminate your paper and ensure it is as widely read and cited as possible. The SAGE Author Gateway has numerous resources to help you promote your work. Visit the Promote Your Article page on the Gateway for tips and advice. In addition, SAGE is partnered with Kudos, a free service that allows authors to explain, enrich, share, and measure the impact of their article. Find out how to maximise your article’s impact with Kudos.
Any correspondence, queries or additional requests for information on the manuscript submission process should be sent to the Therapeutic Advances in Drug Safety editorial office as follows:
For all commercial sales and sponsorship enquiries, including advertising, reprints and supplements, please contact:
Commercial Sales Team, London, UK Tel: +44 20 7336 1205 Email: reprints@sagepub.co.uk