Systematic Review Pricing

One of the most important services we offer — priced around scope, not a single flat number.

01

Review Planning & Protocol

  • Research question development
  • Review objectives
  • PICO/PICOS/PECO/PICo framework
  • Eligibility criteria
  • Inclusion/exclusion criteria
  • Outcomes and outcome prioritization
  • Study-design criteria
  • Protocol development
  • Protocol registration support
  • Statistical synthesis plan
  • Meta-analysis plan
  • Subgroup/sensitivity analysis plan
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02

Literature Search & Information Retrieval

  • Search strategy development
  • Database selection
  • Keywords and controlled vocabulary
  • Boolean/proximity searching
  • Database-specific search strategies
  • Bibliographic database searching
  • Trial registries
  • Grey literature
  • Citation searching
  • Reference-list searching
  • Search updates
  • Deduplication
  • Search documentation
  • Reproducible search strategies
  • PRISMA-S reporting
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03

Screening & Study Selection

  • Reference management
  • Deduplication
  • Title/abstract screening
  • Full-text screening
  • Eligibility assessment
  • Reviewer calibration
  • Independent screening
  • Conflict resolution
  • Reasons for exclusion
  • Automation-assisted screening where appropriate
  • PRISMA flow diagram
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04

Data Extraction & Evidence Tables

  • Data-extraction form development
  • Pilot extraction
  • Study characteristics
  • Participant characteristics
  • Intervention/exposure characteristics
  • Comparator characteristics
  • Outcome data
  • Effect estimates
  • Follow-up periods
  • Funding/conflict information
  • Missing-data assessment
  • Data verification
  • Evidence tables
  • Study characteristics tables
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05

Critical Appraisal & Risk of Bias

  • Risk-of-bias tool selection
  • Risk-of-bias assessment
  • Reviewer calibration
  • Independent assessment
  • Consensus resolution
  • Domain-level judgments
  • Overall risk-of-bias judgments
  • Risk-of-bias tables
  • Risk-of-bias figures
  • Sensitivity analysis based on risk of bias
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06

Evidence Synthesis

  • Narrative synthesis
  • Descriptive synthesis
  • Evidence grouping
  • Structured evidence tables
  • Comparative synthesis
  • Quantitative synthesis
  • Effect-size calculation
  • Data transformation
  • Statistical pooling
  • Heterogeneity assessment
  • Subgroup analysis
  • Sensitivity analysis
  • Meta-regression where appropriate
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07

Meta-Analysis

Where quantitative pooling is appropriate:

  • Effect-size calculation
  • Mean differences
  • Standardized mean differences
  • Risk ratios
  • Odds ratios
  • Hazard ratios
  • Fixed-effect models
  • Random-effects models
  • Heterogeneity analysis
  • Forest plots
  • Subgroup analysis
  • Sensitivity analysis
  • Meta-regression where appropriate
  • Prediction intervals where appropriate
  • Reporting-bias assessment
  • Funnel plots where appropriate
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08

Certainty & Reporting Bias

  • Reporting-bias assessment
  • Missing-results assessment
  • Publication-bias assessment where appropriate
  • GRADE or other appropriate certainty assessment
  • Summary of Findings tables
  • Evidence certainty interpretation
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09

PRISMA & Manuscript Reporting

  • PRISMA 2020 checklist
  • PRISMA flow diagram
  • PRISMA-S documentation
  • Methods section
  • Results section
  • Evidence tables
  • Risk-of-bias presentation
  • Forest plots
  • Supplementary materials
  • Reporting consistency
  • Manuscript preparation
  • Journal formatting
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Pricing: Custom quotation based on review complexity

Meta-Analysis Services

Quantitative synthesis of evidence across studies using appropriate statistical methods, effect measures, models, and sensitivity analyses.

01

Meta-Analysis Planning & Statistical Protocol

  • Research question and estimand clarification
  • PICO/PICOS/PECO framework
  • Meta-analysis objectives
  • Outcome definition and prioritization
  • Selection of eligible study designs
  • Definition of intervention/exposure and comparator groups
  • Statistical analysis plan
  • Choice of effect measure
  • Choice of meta-analysis model
  • Planned subgroup analyses
  • Planned sensitivity analyses
  • Handling of multiple outcomes
  • Handling of multiple time points
  • Handling of multiple reports from the same study
  • Protocol development and registration support
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02

Data Preparation & Effect-Size Extraction

  • Data extraction for meta-analysis
  • Study-level data organization
  • Extraction of reported effect estimates
  • Standardization of outcome measures
  • Mean and standard deviation extraction
  • Event and sample-size extraction
  • Confidence interval and standard-error extraction
  • Conversion of reported statistics
  • Calculation of missing standard errors
  • Conversion between compatible effect measures where appropriate
  • Correlation/dependency adjustments
  • Handling of multiple intervention or comparator groups
  • Handling of repeated measurements
  • Identification of duplicate/overlapping study populations
  • Data checking and verification
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03

Effect-Size Calculation

Continuous outcomes

  • Mean Difference (MD)
  • Standardized Mean Difference (SMD)
  • Hedges' g
  • Change-score effects
  • Endpoint effects

Dichotomous outcomes

  • Risk Ratio (RR)
  • Odds Ratio (OR)
  • Risk Difference (RD)

Time-to-event outcomes

  • Hazard Ratio (HR)

Other effect measures where appropriate

  • Correlation coefficients
  • Prevalence/proportion estimates
  • Incidence/rate ratios
  • Diagnostic accuracy measures
  • Other study-design-specific effect measures
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04

Meta-Analytic Models

  • Fixed-effect models
  • Random-effects models
  • Choice and justification of model
  • Estimation of between-study variance
  • Alternative estimators of heterogeneity
  • Small-study considerations
  • Robust approaches where appropriate
  • Multilevel/multivariate meta-analysis where appropriate
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05

Heterogeneity Assessment

  • Cochran's Q
  • I² statistic
  • Between-study variance (τ²)
  • Prediction intervals
  • Clinical heterogeneity
  • Methodological heterogeneity
  • Statistical heterogeneity
  • Interpretation of heterogeneous findings
  • Investigation of potential sources of heterogeneity
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06

Subgroup & Moderator Analysis

  • Pre-specified subgroup analysis
  • Clinical subgroup analysis
  • Methodological subgroup analysis
  • Population characteristics
  • Intervention characteristics
  • Comparator characteristics
  • Study-design characteristics
  • Geographic/regional differences
  • Follow-up duration
  • Risk-of-bias subgroups
  • Moderator analysis
  • Meta-regression where appropriate
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07

Sensitivity & Robustness Analysis

  • Leave-one-out analysis
  • Influence analysis
  • Exclusion of high-risk-of-bias studies
  • Alternative statistical models
  • Alternative effect measures
  • Alternative assumptions
  • Outlier/influential-study assessment
  • Alternative eligibility criteria
  • Analysis of methodological decisions
  • Robustness of pooled estimates
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08

Advanced Meta-Analysis

Where appropriate:

  • Multivariate meta-analysis
  • Multilevel meta-analysis
  • Network meta-analysis
  • Diagnostic test accuracy meta-analysis
  • Prevalence meta-analysis
  • Incidence/rate meta-analysis
  • Prognostic-factor meta-analysis
  • Meta-analysis of proportions
  • Individual participant data (IPD) meta-analysis support
  • Dose-response meta-analysis
  • Non-linear dose-response analysis
  • Time-to-event meta-analysis
  • Longitudinal/repeated-measures meta-analysis
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09

Publication & Reporting Bias

  • Assessment of small-study effects
  • Funnel plots
  • Egger-type tests where appropriate
  • Selective reporting assessment
  • Missing-results considerations
  • Sensitivity to potentially missing studies/results
  • Appropriate publication/reporting-bias methods
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10

Meta-Analysis Visualization

  • Forest plots
  • Funnel plots
  • Influence plots
  • Galbraith/radial plots where appropriate
  • Bubble plots for meta-regression
  • Subgroup forest plots
  • Prediction-interval visualization
  • Evidence summary figures
  • Publication-quality statistical figures
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11

Evidence Certainty & Interpretation

  • GRADE assessment where appropriate
  • Certainty of evidence
  • Summary of Findings tables
  • Interpretation of pooled effects
  • Clinical/practical interpretation
  • Statistical versus clinical significance
  • Limitations of the evidence
  • Interpretation of heterogeneity
  • Sensitivity of conclusions to analytical assumptions
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12

Results & Reporting

  • Meta-analysis results tables
  • Forest plots
  • Statistical results reporting
  • Methods documentation
  • Results narrative
  • PRISMA-compatible reporting
  • Supplementary statistical materials
  • Reproducible analysis documentation
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Statistical Analysis Services

Comprehensive statistical analysis for research, clinical, healthcare, academic, survey, and organizational datasets.

01

Statistical Analysis Planning

  • Research question development
  • Statistical objectives
  • Hypothesis development
  • Identification of dependent and independent variables
  • Variable classification
  • Selection of appropriate statistical tests
  • Analysis-plan development
  • Power/sample-size considerations
  • Primary and secondary analyses
  • Pre-specified subgroup analyses
  • Sensitivity analyses
  • Statistical reporting plan
02

Data Management & Preparation

  • Data cleaning
  • Data validation
  • Data restructuring
  • Variable coding
  • Data labeling
  • Data-type checking
  • Duplicate detection
  • Missing-data assessment
  • Outlier identification
  • Data consistency checks
  • Data transformation
  • Derived-variable creation
  • Dataset documentation
  • Analysis-ready dataset preparation
03

Descriptive Statistics

  • Frequencies
  • Percentages
  • Mean
  • Median
  • Standard deviation
  • Variance
  • Range
  • Interquartile range
  • Percentiles
  • Confidence intervals
  • Distribution summaries
  • Cross-tabulations
  • Descriptive tables
  • Participant/sample characteristics
04

Data Visualization

  • Histograms
  • Box plots
  • Bar charts
  • Stacked charts
  • Scatterplots
  • Line charts
  • Distribution plots
  • Correlation plots
  • Statistical charts
  • Publication-quality figures
  • Research dashboards
  • Interactive visualizations where appropriate
05

Assumption & Diagnostic Testing

  • Normality assessment
  • Homogeneity of variance
  • Linearity
  • Independence
  • Multicollinearity
  • Homoscedasticity
  • Residual diagnostics
  • Influential observations
  • Model-fit assessment
  • Distributional assumptions
  • Appropriate transformation
  • Robust/non-parametric alternatives where necessary
06

Hypothesis Testing

Parametric tests

  • One-sample t-test
  • Independent-samples t-test
  • Paired-samples t-test
  • ANOVA
  • Repeated-measures ANOVA
  • ANCOVA

Non-parametric tests

  • Mann-Whitney U
  • Wilcoxon signed-rank
  • Kruskal-Wallis
  • Friedman test

Categorical analysis

  • Chi-square test
  • Fisher's exact test
  • McNemar's test
  • Tests of proportions
07

Correlation & Association

  • Pearson correlation
  • Spearman correlation
  • Kendall's tau
  • Partial correlation
  • Correlation matrices
  • Association between categorical variables
  • Effect-size interpretation
08

Regression Analysis

Linear regression

  • Simple linear regression
  • Multiple linear regression
  • Model selection
  • Coefficient interpretation
  • Confidence intervals
  • Prediction

Logistic regression

  • Binary logistic regression
  • Multivariable logistic regression
  • Odds ratios
  • Model diagnostics
  • Classification performance

Other regression models

  • Ordinal logistic regression
  • Multinomial logistic regression
  • Poisson regression
  • Negative binomial regression
  • Robust regression
  • Generalized linear models
09

Advanced Statistical Modeling

Where appropriate:

  • Mixed-effects models
  • Multilevel/hierarchical models
  • Generalized estimating equations
  • Generalized linear mixed models
  • Longitudinal data analysis
  • Repeated-measures modeling
  • Panel-data analysis
  • Time-series analysis
  • Latent-variable models
  • Structural equation modeling
10

Survival & Time-to-Event Analysis

  • Kaplan-Meier analysis
  • Log-rank test
  • Cox proportional hazards regression
  • Hazard ratios
  • Survival curves
  • Proportional-hazards assessment
  • Multivariable survival models
  • Time-to-event interpretation
11

Clinical & Epidemiological Analysis

  • Risk ratios
  • Odds ratios
  • Rate ratios
  • Incidence rates
  • Prevalence analysis
  • Diagnostic test analysis
  • Sensitivity and specificity
  • Positive/negative predictive values
  • ROC analysis
  • AUC
  • Confounding assessment
  • Effect modification
  • Stratified analysis
  • Epidemiological study analysis
12

Survey & Questionnaire Analysis

  • Survey data cleaning
  • Likert-scale analysis
  • Frequency analysis
  • Cross-tabulation
  • Scale scoring
  • Reliability analysis
  • Cronbach's alpha
  • Item analysis
  • Exploratory factor analysis
  • Confirmatory factor analysis where appropriate
  • Survey-weighted analysis where appropriate
  • Demographic subgroup analysis
13

Multivariate & Dimension-Reduction Analysis

Where appropriate:

  • Principal Component Analysis (PCA)
  • Exploratory Factor Analysis (EFA)
  • Confirmatory Factor Analysis (CFA)
  • Cluster analysis
  • Discriminant analysis
  • Multivariate analysis of variance
  • Canonical correlation
  • Dimension-reduction methods
14

Missing Data & Sensitivity Analysis

  • Missing-data assessment
  • Missingness patterns
  • Complete-case analysis
  • Multiple imputation
  • Sensitivity analysis
  • Comparison of analytical assumptions
  • Robustness assessment
15

Causal & Observational Analysis

For appropriately designed studies:

  • Confounding assessment
  • Propensity-score methods
  • Matching
  • Inverse probability weighting
  • Adjustment strategies
  • Mediation analysis
  • Moderation/interaction analysis
  • Treatment-effect estimation
  • Sensitivity analyses
16

Predictive Modeling & Machine Learning

  • Predictive modeling
  • Classification
  • Regression prediction
  • Feature selection
  • Cross-validation
  • Model performance assessment
  • ROC/AUC
  • Calibration
  • Decision thresholds
  • Basic machine-learning models
17

Sample Size & Power Analysis

  • Sample-size calculations
  • Power analysis
  • Effect-size assumptions
  • Two-group comparisons
  • ANOVA designs
  • Correlation studies
  • Regression
  • Proportion estimates
  • Survival analysis
  • Repeated-measures designs
  • Clustered studies
  • Sensitivity analysis for sample-size assumptions
18

Statistical Reporting & Interpretation

  • Statistical results tables
  • APA-style statistical reporting
  • Publication-ready tables
  • Publication-ready figures
  • Results interpretation
  • Effect-size reporting
  • Confidence intervals
  • P-value interpretation
  • Model-result interpretation
  • Statistical-methods documentation
  • Results-section support
  • Reproducible analysis documentation

Statistical Software: R • SPSS • Stata • Python • Excel

What Determines Your Project Cost?

Every research project is different. Here is what actually drives the scope — and the quote — behind each one.

01. Scope & Study Volume

The two biggest drivers for evidence-synthesis projects are how much literature must be searched and how much evidence must be processed. Searching two databases is a different project from searching six. Screening 500 records is different from screening 14,000. We estimate the likely workload from your research question, eligibility criteria, databases, and the literature density of your field before preparing the quote.

Example. A focused clinical question searched across PubMed and Cochrane may produce 800 records and 22 eligible studies. A broader public-health question searched across six databases, trial registries, and grey literature may produce 14,000 records and 80 included studies.

02. Statistical & Methodological Complexity

Not all analyses require the same level of statistical work. A standard pairwise meta-analysis with 12 effect sizes is substantially different from a network meta-analysis, individual participant data synthesis, dose-response analysis, Bayesian model, or prognostic-factor meta-analysis. We scope the project according to the methods required, rather than applying a generic hourly calculation.

Example. A standard random-effects meta-analysis with predefined subgroup and sensitivity analyses has a different scope from a network meta-analysis involving 12 treatment comparisons, network consistency assessment, and treatment-ranking analyses.

03. Risk of Bias & Quality Assessment

The assessment tool, number of studies, study designs, and review process all affect the workload. A review of randomized trials using RoB 2 has different requirements from an observational review using ROBINS-I. Diagnostic accuracy reviews may require QUADAS-2, while umbrella reviews may require tools such as AMSTAR 2.

Where appropriate, additional work may include independent assessments, reviewer calibration, disagreement resolution, domain-level judgments, and presentation of risk-of-bias results.

Example. A systematic review containing 18 randomized controlled trials may require RoB 2 assessment across the included studies. An umbrella review containing 35 systematic reviews may require AMSTAR 2 assessment across each review, with substantially more appraisal and verification work.

04. Evidence Synthesis Requirements

The amount and type of synthesis required can significantly change the project scope. A structured narrative synthesis is different from quantitative pooling. Meta-analysis may require effect-size calculation, heterogeneity assessment, subgroup analysis, sensitivity analysis, meta-regression, or reporting-bias assessment.

Example. A review where studies report sufficiently comparable outcomes for one pooled analysis has a different scope from a review requiring multiple outcome-specific meta-analyses, several subgroup analyses, and sensitivity analyses based on risk of bias.

05. Data Quality & Availability

The condition of your data can materially affect the amount of work required. Clean, analysis-ready data is different from a dataset requiring extensive restructuring, variable recoding, missing-data assessment, duplicate checking, or conversion of reported statistics.

For meta-analysis, the same principle applies to study-level reporting. Missing standard deviations, inconsistent outcome definitions, multiple time points, overlapping populations, and incomplete effect estimates can require additional methodological work.

Example. A dataset with clearly labelled variables and complete outcome measures can move directly into analysis. A dataset containing inconsistent coding, substantial missingness, duplicate records, and multiple versions of the same variables requires additional preparation before statistical analysis can begin.

06. Project Starting Point

The amount of work required also depends on what you already have.

A client with a completed protocol, final search results, screened studies, and a clean extraction dataset requires a different scope from a client starting with only a research question.

Example. “I have extracted data from 25 studies and need the meta-analysis” is a substantially different project from “I have a research question and need the complete systematic review from protocol through reporting.”

07. Required Deliverables

The final deliverables affect project scope as well. These may include:

  • Statistical analysis datasets
  • Evidence tables
  • Risk-of-bias tables and figures
  • Forest plots
  • Funnel plots
  • PRISMA flow diagrams
  • PRISMA checklists
  • GRADE Summary of Findings tables
  • Statistical results tables
  • Publication-ready figures
  • Analysis code
  • Reproducibility files
  • Methods and results documentation

Example. A statistical analysis requiring a cleaned dataset and results tables has a different scope from one requiring a cleaned dataset, reproducible R code, publication-quality figures, formatted tables, and manuscript-ready statistical reporting.

08. Reporting & Publication Requirements

Your intended journal, institution, funder, or reporting framework can affect the level of documentation and analysis required. Requirements may include PRISMA 2020 reporting, PRISMA-S search documentation, GRADE certainty assessment, Summary of Findings tables, supplementary materials, reproducible analysis files, or journal-specific formatting.

We scope these requirements based on the actual target journal and study type, rather than assuming that journal prestige alone determines the workload.

Example. A systematic review intended for a journal requiring detailed PRISMA 2020 reporting, GRADE Summary of Findings tables, extensive supplementary materials, and reproducible statistical documentation requires a different reporting scope from a project with a simpler reporting specification.

09. Delivery Timeline

The methodology does not change simply because a project is urgent, but scheduling does. Rush projects require priority allocation of research and statistical capacity, while standard projects can follow the normal production schedule.

We therefore price accelerated delivery separately where it requires priority scheduling. We do not reduce methodological standards to meet a shorter deadline.

Example. A manuscript needed for a submission deadline in 10 days requires priority scheduling. A thesis analysis due in eight weeks can normally follow the standard production schedule.

10. Research Integrity & Contribution Disclosure

We provide methodological, analytical, and research-support services within appropriate academic and professional standards. Where our contribution meets the criteria for acknowledgement, contributorship, or other disclosure under the relevant journal, institutional, or professional requirements, we support accurate disclosure.

The appropriate form of attribution depends on what work was performed and the policies governing your project. We do not misrepresent authorship, contributions, or the origin of research work.

Example. A project involving statistical consultation may appropriately acknowledge the statistical contribution. A substantial methodological contribution to study design or analysis may require a different form of contributor recognition, depending on the applicable authorship and journal criteria.

A Simple, No-Pressure Quoting Process

No discovery call. No sales follow-ups. Just a clear, itemized quote you can review and consider at your own pace.

1

Tell Us About Your Project

Submit your details through our form, WhatsApp, or email. It takes about five minutes. Share your research question, target journal (if you have one), and approximate timeline.

2

We Review Your Requirements

We assess your project scope and brief a methodologist, usually within a few business hours. If anything needs clarification, we’ll send a few focused questions before preparing your quote.

3

Receive Your Itemized Quote

You’ll get a written breakdown of the project scope, deliverables, timeline, assigned project lead, pricing, and any exclusions. Review everything when it suits you—there’s no call or commitment required.

4

Approve the Quote & Make Payment

When you’re ready, approve the quote and pay securely through a card payment link. Any work outside the agreed scope will be discussed and quoted separately before proceeding.

5

Your Project Gets Underway

Once payment clears, work is scheduled to begin the next business day. You’ll receive progress updates at key milestones and have a dedicated project manager you can contact directly.

What's Included — and What Isn't

Our quotes are designed to be transparent from the beginning. You will know what is included, what is outside scope, and what would require an additional fee before work begins.

Always Included in Every Quote

Every project includes the core professional support and documentation required to complete the agreed scope.

  • PhD-level methodological oversight — A qualified methodologist is assigned as project lead for the full duration of the project.
  • Dedicated project manager — A direct point of contact available during business hours for project coordination, updates, and questions.
  • Unlimited revisions within the agreed scope — We refine the work as needed until it meets the requirements defined in your approved project scope.
  • Reproducible statistical analysis code — R or Stata code is provided for projects involving statistical analysis, where applicable.
  • PRISMA documentation — PRISMA 2020 flow diagram and complete search documentation for systematic reviews, with the appropriate reporting framework used for other review types.
  • Risk-of-bias assessment — Appropriate assessment using tools such as RoB 2, ROBINS-I, Newcastle-Ottawa Scale, QUADAS-2, or another design-appropriate instrument.
  • Publication-ready statistical outputs — Forest plots and other agreed statistical figures are prepared in publication-ready format where applicable.
  • Certainty-of-evidence assessment — GRADE assessment and Summary of Findings tables are included for systematic reviews and meta-analyses where GRADE is appropriate to the review question and evidence type.
  • Confidential handling of your materials — Your data, documents, results, and research materials are never shared or reused for another project without your written permission.
  • First-round response-to-reviewers support — If your manuscript is returned with reviewer comments, we provide support for the first round of methodological and statistical responses within the original project scope.
What This Means for You. No hidden methodological charges. No surprise analysis fees. No paying extra for the basic documentation required to deliver the work properly.

What Is Not Included

Some costs or requests fall outside the standard project scope. If they become relevant, we will identify them before the additional work is performed.

  • Journal submission fees and article processing charges (APCs) — Fees charged directly by journals, including open-access publication charges.
  • External language editing or translation — Professional language editing, translation, or substantial rewriting of source material may require a separate service.
  • Closed-access database or information-resource fees — Subscription or access charges for databases that are not available through your institution or existing access arrangements.
  • Additional analyses outside the approved scope — New research questions, outcomes, datasets, statistical models, subgroup analyses, or substantial methodological changes requested after scope approval are quoted separately.
  • Expedited work outside the agreed timeline — Rush revisions or additional work requiring priority scheduling may incur an expedited-service fee.
  • Premium statistical software or third-party licenses — Paid software, specialized databases, or other third-party tools required specifically for your project are not included unless explicitly stated in the quote.
  • Substantial scope changes following new evidence or data — Major changes arising from newly identified studies, additional datasets, revised eligibility criteria, or a materially changed research question may require re-scoping.
  • Services outside the agreed deliverables — Manuscript preparation, extensive journal formatting, additional figures, supplementary analyses, or other deliverables not specified in the approved scope are quoted separately.
Our No-Surprise Pricing Policy. If something falls outside your approved scope, you will receive a separate line-item quote before the work is done. You decide whether to add it. Nothing is billed after the fact.

Frequently Asked Questions

Can I get a fixed price?

Yes. Once we understand the scope, we can provide a fixed project quotation for most projects.

Can I request only part of a systematic review?

Yes. Clients can request individual components such as search strategy development, screening, data extraction, risk-of-bias assessment or statistical synthesis.

Do you work with existing datasets?

Yes.

Which statistical software do you use?

Excel, SPSS, R and Stata, depending on the analysis.

Can you work with RevMan?

Yes, where appropriate for systematic-review/meta-analysis workflows.

Can you create publication-quality figures?

Yes.

Can you work with qualitative data?

Yes. Depending on the project, this can include coding, thematic analysis, content analysis and qualitative evidence synthesis.

Can you handle urgent projects?

Priority/urgent projects may be available depending on current capacity and project complexity.

Do you provide revisions?

Yes, according to the agreed scope.

How do I get started?

Submit your project details through the quote form, and we'll review the requirements and provide an estimate.

Professional research support without one-size-fits-all pricing.

Tell us what you're trying to accomplish, and we'll recommend the appropriate service, scope and deliverables before you commit.