Academic · Secondary line
We work online with clinicians and academics across all specialties. Processes are carried out in compliance with PROSPERO, PRISMA 2020, RoB 2, GRADE, TRIPOD, and ICMJE Vancouver criteria. The 11 services below are grouped into four tiers.
Most requested
Publication-ready analysis with SPSS / R / Python, major revision defense, and 48-hour urgent delivery before the jury.
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End to end, from PROSPERO registration to the PRISMA 2020 flow, from R metafor / RevMan meta-analysis to GRADE.
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Tier 1
Thesis, revision, and manuscript work under deadline pressure
01
I take your thesis and manuscript statistics to a publication-ready output: analysis, interpretation, and tables with SPSS, R, and Python. A 48-hour rush delivery option is available before the defense.
Duration: 1-2 weeks · Contact for pricing
02
Methodological defense against reviewer objections from the journal, with reanalysis if needed. SPSS / R outputs plus technical text that can be integrated into the author response letter. Delivered on 2-week deadlines.
Duration: 2 weeks · Contact for pricing
03
Methodological assessment of the statistics section for manuscripts you are refereeing. Identification of gaps, alternative analysis suggestions, and compliance checks against RoB and reporting standards.
Duration: 3-5 days · Contact for pricing
Tier 2
PROSPERO-registered, PRISMA 2020-compliant, aimed at international peer-reviewed publication
04
PICO question, search strategy, eligibility criteria, RoB / NOS / QUADAS-2 plan, extraction form, and text ready for the PROSPERO form.
Duration: 2-3 weeks · Contact for pricing
05
End-to-end execution from protocol to publication: multi-database search, dual independent screening, RoB assessment, extraction, PRISMA flow diagram, narrative synthesis, and manuscript draft.
Duration: 4-6 months · Contact for pricing
06
Pooled effect size, heterogeneity analysis (I2, tau2), forest plot, funnel plot, subgroup and sensitivity analyses. In R metafor or RevMan, per your preference. GRADE assessment optional.
Duration: 1-2 months · Contact for pricing
Tier 3
Technical sections of TUBITAK, TEYDEB, and ethics committee applications
07
A 10-15 page technical section for 1001, 1002, and 3501 applications: data requirements, sampling, RoB measures, DMP, and risk-mitigation plan. Feasibility assessment included.
Duration: 3-4 weeks · Contact for pricing
08
R&D technical methodology, verification plan, validation strategy, and TRL assessment for industry and startup applications (1501, 1505, 1507, BiGG).
Duration: 3 weeks · Contact for pricing
09
The methodological section of ethics committee applications: study design, sample size, statistical plan, KVKK-compliant data management, participant safety, and consent protocol.
Duration: 2-3 weeks · Contact for pricing
Tier 4
The technical infrastructure of medical artificial intelligence studies
10
For clinicians and researchers conducting their first artificial intelligence study: study design, ground truth protocol, TRIPOD-compliant validation plan, and technical support for the ethics committee. It starts with the clinical question, not the model.
Duration: 3-4 weeks · Contact for pricing
11
Transformation of raw clinical data (HIS / PACS / Excel) into a research-ready format. KVKK-compliant dataset curation, missing-value handling, harmonization, and version control.
Duration: 4-6 weeks · Contact for pricing
Authorship Policy
In paid consulting projects, acknowledgment is the standard approach. A co-authorship offer is considered only if the four ICMJE Vancouver criteria are met (substantial conceptual/methodological contribution, drafting or critical revision, final approval, and accountability). Offers of authorship in exchange for a fee discount are declined.
For a detailed process description, see the Process page.
First Step
I listen to your situation, clarify the scope, and then send a written quote.
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