Author Guidelines for British Journal of Pharmacology
BJP reporting policies
Approved Abbreviations List
BJP Publication Ethics Policy
Declaration of Transparency and Scientific Rigour - in English
Declaration of Transparency and Scientific Rigour - in Chinese
How to Link to the Guide to Pharmacology
- Aims and Scope
- Manuscript Categories and Requirements
- Preparing the Submission
- Editorial Policies and Ethical Considerations
- Author Licensing
- Publication Process After Acceptance
- Post Publication
- Editorial Office Contact Details
Authors should kindly note that submission implies that the content has not been published or submitted for publication elsewhere except as a brief abstract in the proceedings of a scientific meeting or symposium.
Once the submission materials have been prepared in accordance with the Author Guidelines, manuscripts should be submitted online at https://mc.manuscriptcentral.com/bjp
The submission system will prompt corresponding authors to use an ORCID iD (a unique author identifier) to help distinguish their work from that of other researchers. Click here to find out more.
Click here for more details on how to use ScholarOne.
For help with submissions, please contact BJPedoffice@wiley.com.
The British Journal of Pharmacology is a broad-based journal giving leading international coverage of all aspects of experimental pharmacology. The journal publishes high quality original research, authoritative reviews, Letters to the Editor and commentaries.
Review articles are normally commissioned, but consideration will be given to unsolicited contributions. Each year a range of themed issues are published and the Concise Guide to Pharmacology, a snapshot of the BPS/IUPHAR Guide to Pharmacology database, is published biennially.
Commentaries are invited by the Editor-in-Chief on articles published in the journal.
Letters to the Editor are acceptable where they are a comment on a paper published in the journal or relate to current issues pertinent to the field of Pharmacology.
BJP does not publish work on the actions of biological extracts of unknown chemical composition (e.g. unpurified and unvalidated) or unknown concentration. Papers that involve investigations on tobacco, smoking, alcohol, cocaine and other substances of abuse, whether directly or in the context of their use to generate a disease model (eg smoking for pulmonary disease), will be considered on scientific merit (which includes ethical justification) and relevance to pharmacology.
i. Research Articles
Word limit: 4,000 words maximum, excluding abstract, methods, references and figure legends.
Abstract: 250 words maximum; must be structured, under the following sub-headings: Background and Purpose, Experimental Approach, Key Results, Conclusion and Implications. Minimise abbreviations and do not include any references.
Methods: Methods should be fully transparent with sufficient detail to enable reproducibility by others. There is no word limit for methods.
Discussion and Conclusions: Should not exceed 1,500 words.
References: Maximum of 60 references.
Figures/Tables: Total of no more than 10 figures and tables.
Description: The scope should be pharmacological, i.e. focus on drugs and/or drug targets by characterising novel effects or mechanisms, or by validating new analytical approaches, methods or models and must constitute a significant contribution to pharmacological knowledge. Papers that reassess pharmacological concepts based on earlier results, and purely theoretical papers, will be considered. Papers describing new methods in pharmacology that embody new principles are also welcome.
ii. Review Articles
Word limit: 5,000 words maximum, excluding abstract, references and figure legends.
Abstract: 150 words maximum; must be non-structured.
References: Maximum of 60 references.
Structure: Authors should break up their reviews into headed sections.
Figures/Tables: There should be a minimum of two figures one of which should illustrate the major findings/pathways discussed. There should be a total of no more than 5 figures and tables (combined). The use of explanatory figures in the form of cartoons, flow diagrams, etc., is encouraged. Professional assistance can be provided – please contact the editorial office.
Description: Reviews are comprehensive analyses of the pharmacological literature.
Authors of unsolicited reviews must submit them directly to ScholarOne, following the standard submission procedure.
Word limit: 1,200 words maximum, excluding references.
Abstract: There should be no abstract and no structuring to Commentaries.
References: Maximum of 5 references.
Description: Commentaries on BJP published research are invited only. They should contain no new or unreviewed data.
iv. Letters to the Editor
Word limit: 800 words maximum, excluding references.
Abstract: There should be no abstract and no structuring to Letters.
References: Maximum of 5 references.
Description: Letters should contain no new or unreviewed data. Any correspondence is limited to specific comments or responses relating to a recent BJP paper and current issues of importance to Pharmacology. Where the letter relates to a recent BJP paper the authors will be invited to reply.
In the Introduction state the background to your work and its purpose. State your hypothesis and questions asked. Provide only essential background. 500 words are generally more than sufficient.
To facilitate complete transparency, ‘Methods’ will not be included in the word count of Research Articles.
Your Methods must be described in sufficient detail to allow the experiments to be interpreted and repeated by an experienced investigator. Where published methods are used, references should be given, together with a brief outline: any references must provide the full description and not be a signpost to another reference. If this is a problem please provide the full description of the method in your own manuscript.
For experimental studies, the methods should be presented in sections and should cover
Test systems used (animal preparations, isolated tissues, cultured cells, in vitro systems, etc.) and the measurements made (with technical details) for each system
Where animals have been used as a test system the Journal has strict requirements for the reporting of experiments involving animals or animal tissue (adherence to ARRIVE and BJP guidelines should be stated in this section).
We encourage authors to show examples of typical westerns/PCRs with associated quantitative data where such experimentation has been conducted. However, where these methods have been used, authors should also provide a single PDF of all original western blots used for each data set. For each data set the gel/blot images should be provided and labelled according to figure number. This single PDF should be uploaded as supplementary material. This images will not be published and will be used for the review process only.
Experimental protocols and design (adherence to BJP guidelines should be stated in this section)
Data and statistical analysis (adherence to BJP guidelines should be stated in this section)
For all studies, experimental design, data analysis and statistical procedures should be consistent with the principles explained in the editorial Experimental design and analysis and their reporting: new guidance for publication in BJP, and the major points detailed below. (For a precise bullet list, please see the Declaration of Transparency and Scientific Rigour.)
Authors should ensure that for each test system used the following information is provided within the methods. Authors should follow the guidance provided at the bullets.
For the rationale, please read Curtis et al., 2015.
For help with designing your experiments, please see the NC3Rs Experimental Design Assistant.
Explain how you have determined/designed group sizes. These should be equal by design, and any variation owing to experimental losses or violation of predetermined exclusion criteria must be explained.
BJP accepts the use of post-hoc statistical tests designed to identify outliers within datasets. These tests should be appropriate for the type (distribution) of data being analysed. Examples of such tests include Grubb’s or ROUT outlier tests. Where outliers are identified a clear indication of number of data points excluded must be provided with a robust explanation for the type of test used.
The principle is that you should provide the exact group size (n) for each experimental group/condition, not a range; and n refers to independent values, not replicates. Data subjected to statistical analysis should have a group size (n) ≥ 5. If n is less than 5 anywhere in the study, please provide an explanation, and please do not undertake statistical analysis of the dataset.
Please state whether animals or human subjects were randomised for treatment. If randomisation was not carried out, state that randomisation was not used, and please supply an explanation for why not.
Please state whether the operator and data analysis were blinded. If blinding was not undertaken, or not feasible, please state why.
When normalisation is employed (e.g. expression of values as ‘% of baseline’ or ‘fold mean control’) please provide a valid scientific justification (i.e. to control for unwanted sources of variation).
If employing normalisation that generates control or baseline values with no variance (standard deviation = 0), please explain with a valid scientific justification and do not subject such data to parametric statistical analysis.
Please explain any data transformation (such as log transformation) with a valid scientific justification (i.e. to generate a Gaussian-distributed data set amenable to parametric analysis).
Data and Statistical analysis
This section is mandatory in all manuscripts and should be inserted in to the methods as a sub-heading and include the statement that ‘the data and statistical analysis comply with the recommendations on experimental design and analysis in pharmacology (Curtis et al., 2015).’
Provide details of any statistical package or program employed, including manufacturer and model number and details of which tests (and which options) and which program(s) (with full version number) were used.
If an experiment (e.g. assay) is undertaken in duplicate, triplicate etc., please state that technical replicates were used to ensure the reliability of single values. This reliability can be quoted as a coefficient of variation. In data analysis and data presentation use the single values (i.e. 5 samples each run in triplicate is n=5 not n=15).
When comparing groups, and if a level of probability (P) is deemed to constitute the threshold for statistical significance, define this here in the ‘Data and Statistical Analysis’ section of the Methods, and do not vary it later in Results (by presentation of multiple levels of significance). Thus if P<0.05 is defined as threshold, P<0.01 etc. should not appear in the results. However, setting P at a lower value such as P<0.01 or 0.001 is quite acceptable, provided that this is defined as constituting statistical significance, and is not varied. It is not necessary to state the exact level of P.
Studies employing animals, animal tissues or primary cultures from animal tissues must provide additional detail covering the requirements for reporting experiments involving animals or animal tissue, as detailed below.
Requirements for reporting experiments involving animals or animal tissue
This information is required only if animals, animal tissue or primary cultures are involved. It allows you to comply with BJP Policy on reporting experiments involving animals and with the principles of ARRIVE and the United States NIH. Please ensure that this section contains the details described as follows.
Validity of animal species or model selection
Provide a scientific justification for the animal species and each model selected for study. For instance, ‘this model of pain in rats has been in use for several years (reference)’ (refer to review on pain models).
Make a statement of ethical approval for experimentation that will be recognised worldwide. Indicate the nature of the ethical review permissions, and national or institutional guidelines for the care and use of animals, that cover the research. Include application approval numbers and web addresses of the approving organisations, if available.
For further details, please see the Ethics Section below.
Please note source, species, strain, sex, age range, weight and any additional data that are relevant to the study.
Housing and husbandry
Standard animal housing and care does not need to be explained in detail as long as these meet the standards required by relevant local guidance or law.
Provide details of non-standard housing (type of facility e.g. specific pathogen free [SPF]; type of cage or housing; bedding material; number of cage companions; tank shape and material etc. for fish).
Provide details, as appropriate, of behavioural tests, anaesthesia and analgesia, surgical procedures, how the animal was killed and, if there is recovery following surgery, the methods of asepsis and post-operative care. Include welfare-related assessments, measurements and interventions (e.g. humane end points) that were carried out prior to, during, or after the experiment.
Finally, please end your Methods section with the Materials sub-section. Provide the suppliers (names and addresses [city and country only) of drugs and other chemicals, reagents and other materials.
For new compounds, the synthesis and physicochemical characteristics of the compound(s) must be summarised here unless these have already been published in another journal or in a patent.
Please note BJP will not consider manuscripts concerning or using compounds of undisclosed structure or undefined mixtures of compounds e.g. plant extracts.
In this section, please do not repeat numerical values of any data presented in tables or figures. Each value should be shown EITHER in the Tables or Figures OR in the text, NOT both. When a change is statistically significant, there is no need to show P<0.05 etc. in the text, as this level will have already been given in the Methods (data analysis) and ONLY ONE VALUE of P should be used throughout the manuscript.
Do not interpret, compare or discuss the data reported in the Results section; it is more appropriate to do this in the Discussion and Conclusions.
Discussion and Conclusions
Please note this section is normally restricted to 1,500 words and Senior Editors will ask for justification when this limit is exceeded.
Explain how your hypothesis or initial questions have been addressed by your results and why this is important.
Make a statement concerning the possible clinical relevance of the study.
If your study has any implications for the 3Rs (replacement, refinement or reduction), please make a statement on this in the Discussion, e.g. ‘When used in signalling assays, the above procedure results in one rat pup yielding approximately 8 data points for neurons and 24 data points for glia. This is a significant enhancement over previous studies examining cAMP signalling, where approximately two rat pups have yielded a single data point for trigeminal ganglia-derived neurons’ (Walker et al., British Journal of Pharmacology. 2014)
Cover letters are not required or indeed mandatory; however, they may be supplied at the author’s discretion (but should not be included as part of the manuscript).
Parts of the Manuscript
The manuscript should be submitted in separate files: main text file; figures.
Main Text File
The text file should be presented in the following order:
ii. A short running title of less than 60 characters
iii. The full names of the authors
iv. The author's institutional affiliations where the work was carried out, with a footnote for the author’s present address if different from where the work was carried out
vi. Abstract and keywords
vii. Main text
ix. Tables (each table complete with title and footnotes)
x. Figure legends
xi. Appendices (if relevant). Figures and supporting information should be supplied as separate files.
Title. The title should be short and informative, containing major keywords related to the content. It must clearly indicate the subject matter of the paper, why the work is important and any assertions it contains must be justified by the results presented in the paper The title should not contain abbreviations, cumbersome technical terms or technical details (see Wiley's best practice SEO tips).
Acknowledgements. Contributions from individuals who do not meet the criteria for authorship should be listed, with permission from the contributor, in an Acknowledgements section. Financial and material support should also be mentioned. Giving thanks to anonymous reviewers is not appropriate.
Conflict of Interest Statement. Authors will be asked to provide a conflict of interest statement during the submission process. See ‘Conflict of Interest’ section in Editorial Policies and Ethical Considerations for details on what to include in this section. Authors should ensure they liaise with all co-authors to confirm agreement with the final statement.
Abstract Abstracts are required for some manuscript types. For details on manuscript types that require abstracts and/or keywords, as well as how to prepare them, please refer to the ‘Manuscript Types and Criteria’ section. Your Abstract should convey clearly the key messages of the work, and why the work is important.
The journal uses British spelling; however, authors may submit using either option, as spelling of accepted papers is converted during the production process.
Footnotes to the text are not allowed and any such material should be incorporated into the text as parenthetical matter.
References follow the Harvard style, i.e. the author, date system. In the text give the author’s name followed by the year in parentheses: Smith (2000). If several papers by the same authors and from the same year are cited, a,b,c etc. should be inserted after the year of publication. In the reference list, references should be listed in alphabetical order. Reference to unpublished data and personal communications should not appear in the list but should be cited in the text only (e.g. Smith A, 2000, unpublished data).
Submissions are not required to reflect the precise reference formatting of the journal (use of italics, bold etc.), however it is important that all key elements of each reference are included. Please see below for examples of reference content requirements.
Benjamin van Rooij B, Stern RE and Fürst K. The authoritarian logic of regulatory pluralism: Understanding China's new environmental actors. Regulation & Governance 10: 3-13. https://doi.org/10.1111/rego.12074
Fujita M, Krugman P, Venables AJ (2001) The Spatial Economy: Cities, Regions, and International Trade. MIT Press, Cambridge, MA.
Cancer-Pain.org [homepage on the internet]. New York: Association of Cancer Online Resources, Inc.; c2000–01 [Cited 2015 May 11]. Available from: http://www.cancer-pain.org/.
Tables should be numbered consecutively with Arabic numerals. They should be self-contained and should complement, not duplicate, information contained in the text. They should be supplied as editable files, not pasted as images. Legends should be concise but comprehensive – the table, legend and footnotes must be understandable without reference to the text. All abbreviations must be defined in footnotes. Footnote symbols: †, ‡, §, ¶, should be used (in that order) and *, **, *** should be reserved for P-values. Statistical measures such as SD or SEM should be identified in the headings.
Legends should be concise but comprehensive – the figure and its legend must be understandable without reference to the text. Include definitions of any symbols used and explain all units of measurement. Approved abbreviations or abbreviations already defined in the manuscript are permitted. Legends should detail the n values for each data set shown and identify the nature of the group comparisons. For additional detail the authors may wish to explain the exact statistical test utilised.
Figure presentation of data should conform to BJP Guidelines. Please refer to a recent BJP Editorial on this issue. In essence BJP prefers all figures to display data in the most transparent manner. Ideally, data should be presented as scatter plots with a mean and error depicted by lines.
Although authors are encouraged to send the highest-quality figures possible, for peer-review purposes, a wide variety of formats, sizes, and resolutions are accepted. Click here for the basic figure requirements for figures submitted with manuscripts for initial peer review, as well as the more detailed post-acceptance figure requirements.
Figures should be numbered consecutively with Arabic numerals and may comprise several parts (Fig 2A, 2B, 2C etc.). Keys to the different symbols, scatter symbols, bars and lines should be placed in the whole figure and not repeated in the legend.
Figures submitted in colour may be reproduced in colour online free of charge. Please note, however, that it is preferable that line figures (e.g. graphs and charts) are supplied in black and white so that they are legible if printed by a reader in black and white.
Appendices will be published after the references. For submission they should be supplied as separate files but referred to in the text.
Supporting information is information that is not essential to the article, but provides greater depth and background. It is hosted online and appears without editing or typesetting. It may include tables, figures, videos, datasets, etc. Click here for Wiley’s FAQs on supporting information. Information that aids interpretation such as demonstrations of selectivity of an antibody, demographic data of animal or human cohort, typical western blots or immunohistochemical images should be submitted as supporting information, with an explanation of why it is considered supporting, rather than essential to the paper. Please state the number of figures and tables submitted as supporting information (including zero - please add 'None supplied' ).
Note: if data, scripts or other artefacts used to generate the analyses presented in the paper are available via a publicly available data repository, authors should include a reference to the location of the material within their paper.
General Style Points
The following points provide general advice on formatting and style. Be succinct. Stay ‘on topic’. Avoid unsubstantiated speculation. Don’t assume mechanisms when using drugs as tools – selectivity is concentration-dependent. Use correct, clear, plain English.
In general, terms should not be abbreviated unless they are used repeatedly and the abbreviation is helpful to the reader. Initially, use the word in full, followed by the abbreviation in parentheses. Thereafter use the abbreviation only.
There is a list of Approved Abbreviations that do not need to be defined in the manuscript or abstract. All other abbreviations must be defined, as an alphabetical list, and when first used in the text.
Nomenclature used in your article must follow that of the IUPHAR/BPS Guide to PHARMACOLOGY. Should your manuscript be accepted, the key pharmacological targets discussed in your manuscript will ultimately be highlighted in your published article. Apply linking to these ligands and targets within the body of your manuscript. You will also be asked to provide a simple list of ligands and targets you have hyperlinked so that the press editors can check you have included all major targets. This list will not be published.
You will also be asked to supply a standard ‘Nomenclature of Targets and Ligands’ statement.
You are not required to supply these items at submission. They will be requested should your manuscript be accepted. You will be given full and clear instructions on how to fulfil these requirements by the editorial office.
Units of measurement:
Measurements should be given in SI or SI-derived units. Negative index notation (e.g. mg kg−1, pmol mm−2 min−1) should be used rather than solidus notation (e.g. mg/kg, pmol/mm2/min). ‘dL’ is not an SI unit; this is the most common mistake.Visit the Bureau International des Poids et Mesures (BIPM) website at www.bipm.fr for more information about SI units.
Numbers under 10 are spelt out, except for: measurements with a unit (8mmol/l); age (6 weeks old), or lists with other numbers (11 dogs, 9 cats, 4 gerbils).
Chemical substances should be referred to by the generic name only. Trade names should not be used. Drugs should be referred to by their generic names. If proprietary drugs have been used in the study, refer to these by their generic name, mentioning the proprietary name and the name and location of the manufacturer in parentheses.
For new compounds, the synthesis and physicochemical characteristics of the compound(s) must be summarised unless these have already been published in another journal or in a patent.
Please note that the journal will not consider manuscripts concerning or using compounds of undisclosed structure or undefined mixtures of compounds e.g. plant extracts.
Resource Identification Initiative
The journal supports the Resource Identification Initiative, which aims to promote research resource identification, discovery and reuse. This initiative, led by the Neuroscience Information Framework and the Oregon Health & Science University Library, provides unique identifiers for antibodies, model organisms, cell lines, and tools including software and databases. These IDs, called Research Resource Identifiers (RRIDs), are machine-readable and can be used to search for all papers where a particular resource was used and to increase access to critical data to help researchers identify suitable reagents and tools.
Authors are asked to use RRIDs to cite the resources used in their research where applicable in the text, similar to a regular citation or Genbank Accession number. For antibodies, authors should include in the citation the vendor, catalogue number, and RRID both in the text upon first mention in the Methods section. For software tools and databases, please provide the name of the resource followed by the resource website, if available, and the RRID. For model organisms, the RRID alone is sufficient.
Additionally, authors must include the RIIDs in the list of keywords associated with the manuscript.
To Obtain Research Resource Identifiers (RRIDs):
1) Use the Resource Identification Portal, created by the Resource Identification Initiative Working Group.
2) Search for the research resource (please see the section titled “Search Features and Tips” in ABOUT for more information).
3) Click on the “Cite This” button in ABOUT to obtain the citation and insert the citation into the manuscript text.
If there is a resource that is not found within the Portal, authors are asked to register the resource with the appropriate resource authority. Information on how to do this is provided in the “Resource Citation Guidelines” section of the Portal.
If any difficulties in obtaining identifiers arise, please contact email@example.com for assistance.
Antibodies: "Wnt3 was localized using a rabbit polyclonal antibody C64F2 against Wnt3 (Cell Signaling Technology, Cat# 2721S, RRID: AB_2215411)"
Model Organisms: "Experiments were conducted in c. elegans strain SP304 (RRID:CGC_SP304)"
Cell lines: "Experiments were conducted in PC12 CLS cells (CLS Cat# 500311/p701_PC-12, RRID:CVCL_0481)"
Tools, Software, and Databases: "Image analysis was conducted with CellProfiler Image Analysis Software, V2.0 (http://www.cellprofiler.org, RRID:nif-0000-00280)"
Wiley Author Resources
BJP employs Press Editors and Copy Editors, who provide a free language and copy-editing service to improve the quality of all manuscripts that are acceptable for publication on scientific grounds.
Manuscript Preparation Tips: Wiley has a range of resources for authors preparing manuscripts for submission available here. In particular, authors may benefit from referring to Wiley’s best practice tips on Writing for Search Engine Optimization.
Editing, Translation and Formatting Support: BJP employs Press Editors and Copy Editors, who provide a free language and copy-editing service to improve the quality of all manuscripts that are acceptable for publication on scientific grounds. A further service is also available to authors: Wiley Editing Services. This service can greatly improve the chances of a manuscript being accepted. Offering expert help in English language editing, translation, manuscript formatting, and figure preparation, Wiley Editing Services ensures that the manuscript is ready for submission.
Publication on preprint servers
The journal will consider for review articles previously available as preprints on non-commercial servers such as bioRxiv, psyArXiv, SocArXiv, etc, as long as authors have retained copyright of their articles during the preprint process. Authors may also post the submitted version of their manuscript to non-commercial servers at any time. Authors should update any pre-publication versions with a link to the final published article. Allowing submission under such circumstances does not guarantee that an article will be sent out for review or that it will be accepted for publication in BJP.
Editorial Review and Acceptance
Tips for authors on how to navigate the peer review process can be found here.
The acceptance criteria for all papers are the quality and originality of the research and its significance to journal readership. Except where otherwise stated, manuscripts are single-blind peer reviewed. Papers will only be sent to review if the Senior Editors determine that the paper meets the appropriate quality and relevance requirements.
Wiley's policy on confidentiality of the review process is available here.
Once submitted, a manuscript will first be checked by the Editorial Office to ensure all elements have been submitted. If any required documentation is absent, the Editorial Office will return the manuscript to the author and request any missing information or material.
Manuscripts are then given a first review by a Senior Editor (triage), who may return the manuscript to the authors to avoid delay if (s)he judges that it is out of scope or has little chance of being accepted after review. Otherwise it will be sent for review, usually by an Editor and three referees.
The referees’ comments and Editor’s recommendation will be reviewed by the appropriate Senior Editor, who will communicate the decision to the corresponding author. This process takes one month on average from submission to the initial decision, but can take longer.
Authors may be asked to revise their manuscript before a final decision is made.
Once your paper is accepted, you will be asked by the editorial office to send any outstanding essential material. This will include a request that you apply hyperlinking within the body of your manuscript (just to the main ligands and targets discussed in your article). You will be supplied with full instructions.
Data Storage and Documentation
British Journal of Pharmacology encourages data sharing wherever possible (please see the recent BJP guidelines editorial on this issue, unless this is prevented by ethical, privacy, or confidentiality matters. Authors publishing in the journal are therefore encouraged to make their data, scripts and other artefacts used to generate the analyses presented in the paper available via a publicly available data repository; however, this is not mandatory. If the study includes original data, at least one author must confirm that he or she had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
See above for detailed requirements when using animals or animal tissue. Authors should state whether experiments were performed in accordance with relevant institutional and national guidelines for the care and use of laboratory animals:
US authors should cite compliance with the US National Research Council's Guide for the Care and Use of Laboratory Animals, the US Public Health Service's Policy on Humane Care and Use of Laboratory Animals, and Guide for the Care and Use of Laboratory Animals.
UK authors should conform to UK legislation under the Animals (Scientific Procedures) Act 1986 Amendment Regulations (SI 2012/3039).
European authors outside the UK should conform to Directive 2010/63/EU.
Human Studies and Subjects
For manuscripts reporting medical studies that involve human participants, a statement identifying the ethics committee that approved the study and confirmation that the study conforms to recognized standards is required, for example: Declaration of Helsinki; US Federal Policy for the Protection of Human Subjects; or European Medicines Agency Guidelines for Good Clinical Practice.
Images and information from individual participants will only be published where the authors have obtained the individual's free prior informed consent. Authors do not need to provide a copy of the consent form to the publisher; however, in signing the author license to publish, authors are required to confirm that consent has been obtained. Here is the patient consent form.
Clinical Trial Registration
The journal requires that clinical trials are prospectively registered in a publicly accessible database and clinical trial registration numbers should be included in all papers that report their results. Authors are asked to include the name of the trial register and the clinical trial registration number at the end of the abstract. If the trial is not registered, or was registered retrospectively, the reasons for this should be explained.
Research Reporting Guidelines
Accurate and complete reporting enables readers to fully appraise research, replicate it, and use it. Authors are encouraged to adhere to the following research reporting standards, where appropriate.
The journal requires that all authors disclose any potential sources of conflict of interest. Any interest or relationship, financial or otherwise that might be perceived as influencing an author's objectivity is considered a potential source of conflict of interest. These must be disclosed when directly relevant or directly related to the work that the authors describe in their manuscript. Potential sources of conflict of interest include, but are not limited to the following: patent or stock ownership, membership of a company board of directors, membership of an advisory board or committee for a company, and consultancy for or receipt of speaker's fees from a company. The existence of a conflict of interest does not preclude publication. If the authors have no conflict of interest to declare, they must also state this at submission. It is the responsibility of the corresponding author to review this policy with all authors and collectively to disclose with the submission ALL pertinent commercial and other relationships.
Authors should list all funding sources in the Acknowledgments section. Authors are responsible for the accuracy of their funder designation. If in doubt, please check the Open Funder Registry for the correct nomenclature: https://www.crossref.org/services/funder-registry/.
For papers where no conflicts of interest or funding are declared, a default statement is added to that paper.
The list of authors should accurately illustrate who contributed to the work and how. All those listed as authors should qualify for authorship according to the following criteria:
1. Have made substantial contributions to conception and design, or acquisition of data, or analysis and interpretation of data;
2. Been involved in drafting the manuscript or revising it critically for important intellectual content;
3. Given final approval of the version to be published. Each author should have participated sufficiently in the work to take public responsibility for appropriate portions of the content; and
4. Agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Contributions from anyone who does not meet the criteria for authorship should be listed, with permission from the contributor, in an Acknowledgments section (for example, to recognize contributions from people who provided technical help, collation of data, writing assistance, acquisition of funding, or a department chairperson who provided general support). Prior to submitting the article all authors should agree on the order in which their names will be listed in the manuscript.
Additional Authorship Options: Joint first or senior authorship: In the case of joint first authorship, a footnote should be added to the author listing, e.g. ‘X and Y should be considered joint first author’ or ‘X and Y should be considered joint senior author.’
As part of the journal’s commitment to supporting authors at every step of the publishing process, the journal requires the submitting author (only) to provide an ORCID iD when submitting a manuscript. This takes around two minutes to complete. Find more information here.
This journal is a member of the Committee on Publication Ethics (COPE). Note the journal uses iThenticate’s CrossCheck software to detect instances of overlapping and similar text in submitted manuscripts. Read the Top 10 Publishing Ethics Tips for Authors here. Wiley’s Publication Ethics Guidelines can be found at authorservices.wiley.com/ethics-guidelines/index.html.
Submission of a manuscript to BJP will be taken to indicate that
the content of the manuscript is original and that it has not been published or accepted for publication, either in whole or in part, other than as short abstracts, communications or conference proceedings;
no part of the manuscript is currently under consideration for publication elsewhere;
all authors have seen and approved the final version of the submitted paper;
authors have, if necessary, obtained permission to publish from their employers or institutions;
approvals are held from any persons acknowledged, or cited as having provided personal communication;
permission has been obtained to use any copyrighted material, such as reproducing a figure from another article, in print and electronic forms, and that the source of the material has been acknowledged; and
images have not been manipulated outside the CLIP principles.
You must describe and clearly indicate all modifications, selective digital adjustments or electronic enhancements in all digital images. Avoid splicing different gels together. If unavoidable, clearly demark the point of splicing and avoid over-extending quantitative interpretations across splices. As a minimum, provide uncropped data at the submission stage to facilitate peer review.
Contacting the Journal with expressions of concern
BJP is dedicated to correcting errors in the scientific literature – be they errors in data, statistical analysis or of an ethical nature - and doing so quickly, in line with COPE guidelines. As such, please send expressions of concern over BJP published material direct to the journal’s Executive Editor at the Publishers, firstname.lastname@example.org.
For the Journal’s policy on publication misconduct and all other areas of publishing ethics, please see the Journal’s Ethics Policy .
If a paper is accepted for publication, the author identified as the formal corresponding author will receive an email prompting them to log in to Author Services, where via the Wiley Author Licensing Service (WALS) they will be required to complete a copyright license agreement on behalf of all authors of the paper.
Authors may choose to publish under the terms of the journal’s standard copyright agreement, or OnlineOpen under the terms of a Creative Commons Licence.
General information regarding licensing and copyright is available here. To review the Creative Commons Licence options offered under OnlineOpen, please click here. (Note that certain funders mandate a particular type of CC licence be used; to check this please click here.)
Self-Archiving Definitions and Policies: Note that the journal’s standard copyright agreement allows for self-archiving of different versions of the article under specific conditions. Please click here for more detailed information about self-archiving definitions and policies.
Open Access fees: Authors who choose to publish using OnlineOpen will be charged a fee. A list of Article Publication Charges for Wiley journals is available here.
Funder Open Access: Please click here for more information on Wiley’s compliance with specific Funder Open Access Policies.
Linking to the Guide to Pharmacology
When your article is accepted for publication, you will be contacted by the Editorial office to complete a number of tasks required before your article can move into publication. One of these is to apply linking within your article to the Guide to Pharmacology, for all key ligands and targets. Full instructions will be provided, and can be found here.
Accepted Article Received in Production
When an accepted article is received by Wiley’s production team, the corresponding author will receive an email asking them to login or register with Wiley Author Services. The author will be asked to sign a publication licence at this point.
The journal offers Wiley’s Accepted Articles service for all manuscripts. This service ensures that accepted ‘in press’ manuscripts are published online shortly after acceptance, prior to copy-editing or typesetting. Accepted Articles are published online a few days after final acceptance and appear in PDF format only. They are given a Digital Object Identifier (DOI), which allows them to be cited and tracked and are indexed by PubMed. After the final version article is published (the article of record), the DOI remains valid and can still be used to cite and access the article.
Accepted Articles will be indexed by PubMed; submitting authors should therefore carefully check the names and affiliations of all authors provided in the cover page of the manuscript so it is accurate for indexing. Subsequently, the final copyedited and proofed articles will appear in an issue on Wiley Online Library; the link to the article in PubMed will update automatically.
Simultaneous to Accepted article publication, the accepted manuscript is re-formatted into the journal style and then the language and scientific content are checked by a Press Editor. The paper is then typeset.
Once the paper is typeset, the author will receive an email notification with the URL to download a PDF typeset page proof, as well as associated forms and full instructions on how to correct and return the file.
Please note that the author is responsible for all statements made in their work, including changes made during the editorial process – authors should check proofs carefully. Note that proofs should be returned within 72 hours from receipt of first proof.
The journal offers rapid publication via Wiley’s Early View service. Early View (Online Version of Record) articles are published on Wiley Online Library before inclusion in an issue. Note there may be a delay after corrections are received before the article appears online, as Editors also need to review proofs. Once the article is published on Early View, no further changes to the article are possible. The Early View article is fully citable and carries an online publication date and DOI for citations.
Access and Sharing
When the article is published online:
The author receives an email alert (if requested).
The link to the published article can be shared through social media.
The author will have free access to the paper (after accepting the Terms & Conditions of use, they can view the article).
The corresponding author and co-authors can nominate up to ten colleagues to receive a publication alert and free online access to the article.
Full information for authors on sharing content can be found here.
Print copies of the article can now be ordered (instructions are sent at proofing stage or use the below contact details). Email email@example.com.
Promoting your article
To find out how to best promote an article, click here.
Measuring the impact of an article
A video abstract can be a quick way to make the message of your research accessible to a much larger audience. In 2017, Wiley, our Publishers, and its partner Research Square, will be offering, on a trial basis, a service of professionally produced video abstracts, available to authors of five articles selected by the journal. You can learn more about it at www.wileyauthors.com/videoabstracts. Authors of papers selected for this service will be contacted through the editorial office.
To find out how to best promote an article, click here.
10. TRANSFER TO OTHER BRITISH PHARMACOLOGICAL SOCIETY (BPS) JOURNALS
Pharmacology Research & Perspectives is jointly edited on behalf of the BPS and the American Society of Pharmacology and Experimental Therapeutics (ASPET). The Editors of BJP might consider that a submitted manuscript is out of scope and more suitable for consideration by its sister journals British Journal of Clinical Pharmacology ( BJCP) or the open access journal Pharmacology Research & Perspectives. If so, the Editors will offer authors the opportunity to transfer the manuscript to the editorial office of its sister journals for consideration, with no need to reformat the manuscript.
These Author Guidelines were last updated on 19th October 2017.
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