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Services / Capabilities

Built on expertise. Driven by results.

From real-world evidence to strategic insights, CliniWings delivers end-to-end solutions for research, publications, and healthcare decision-making.

The valueSupports regulatory submissions, post-marketing surveillance, real-world treatment effectiveness and optimized healthcare strategy.
Service 01 / 06

Real-World Evidence (RWE) Solutions

Turning complex healthcare data into strategic clarity. We harness claims, EHR, registries, and patient-reported outcomes to deliver evidence that moves decisions - from clinical practice to regulatory submissions.

What we deliver

  • Study design & methodology (retrospective, prospective, observational)
  • Protocol development & cohort definition
  • Data management & integration of real-world datasets
  • Advanced analytics & statistical modeling (regression, survival analysis, propensity score matching)
  • Safety & effectiveness evaluation
  • Health outcomes & utilization studies
Researcher reading a scientific paper for a systematic review
The valueDelivers high-quality evidence, a foundation for HEOR models, strategic decision support, and time and resource efficiency.
Service 02 / 06

Systematic Literature Review (SLR) & Evidence Synthesis

Comprehensive, reproducible, and PRISMA-compliant literature reviews - combining methodological rigor, advanced analytics, and scientific expertise to generate high-quality evidence for regulatory, clinical, and market access decisions.

What we deliver

  • Protocol development (PICO)
  • Comprehensive literature search (PubMed, Embase, Cochrane and specialized databases)
  • Screening & study selection
  • Data extraction & quality assessment
  • Meta-analysis and network meta-analysis (NMA)
  • PRISMA flow diagram & reporting

Review types we deliver

  • Systematic literature review
  • Targeted literature review
  • Rapid evidence review
  • Scoping review
  • Economic & outcomes review
  • Evidence gap assessment
  • SLR update

Review methods are selected for the question and intended use. A targeted or rapid review is described transparently and is not represented as a full systematic review.

Analysts reviewing health economic charts and data
The valueSupports market access and reimbursement, value-based healthcare insights, pricing and payer strategy, and healthcare policy.
Service 03 / 06

Health Economics & Outcomes Research (HEOR)

Demonstrating the true economic and clinical value of your interventions. We combine advanced modeling, health outcomes assessment, and cost analysis to support market access, reimbursement decisions, and value-based healthcare strategies.

What we deliver

  • Cost-effectiveness analysis (CEA)
  • Budget impact analysis (BIA)
  • Quality of life & utility assessments (QALYs)
  • Health economic modeling (Markov, decision tree and simulation models)
  • Scenario & sensitivity analysis
  • Comparative effectiveness research

Evidence we synthesize

  • Cost of illness & HRU
  • Direct & indirect costs
  • HRQoL & patient-reported outcomes
  • Health-state utilities
  • Published CEA, CUA & BIA
  • Economic model inputs
  • Epidemiology
  • Treatment patterns
  • Natural history
Medical writer preparing clinical documents
The valueAll documents follow ICH, GPP3 and other international guidelines, with rigorous review and timely delivery.
Service 04 / 06

Medical & Scientific Writing

Translating complex clinical evidence into compelling communication. Our experienced medical writers help you submit regulatory dossiers, publish research, and communicate value with precision and confidence.

What we deliver

  • Systematic review reports (PRISMA-compliant)
  • Clinical study protocols
  • Clinical study reports (CSR)
  • Value dossiers (AMCP and global value dossiers)
  • Manuscripts, abstracts & conference posters
  • Regulatory submissions support
The valueExperienced medical writers and publication strategists deliver accurate, publication-ready work within project deadlines.
Service 05 / 06

Publication & Research Support

Maximizing the visibility and impact of your scientific research. We support your publications from planning and drafting through to journal and congress submission.

What we deliver

  • Publication planning & strategy
  • Manuscript, abstract & poster development
  • Journal and congress selection
  • Formatting and submission to journal guidelines
  • Response to peer-reviewer comments
  • Quality, accuracy and GPP3-aligned processes

Deliverables can include

  • Technical reports
  • Evidence tables
  • Executive summaries
  • Manuscripts
  • Abstracts
  • Conference posters
  • Presentation content

Authorship, journal requirements, review rounds and submission responsibilities are agreed separately; publication acceptance is not guaranteed.

Pharmaceutical market analytics dashboard
The valueActionable, data-driven insights that help you identify unmet needs, anticipate market shifts and position your portfolio ahead of the competition.
Service 06 / 06

Competitive Intelligence & Landscape Analysis

Gain the strategic edge in a fast-moving healthcare market. We provide deep insights into therapeutic areas, competitor activity, and evolving market trends to help you optimize strategies and respond proactively.

What we deliver

  • Pipeline analysis
  • Competitor benchmarking
  • Clinical trial landscape analysis
  • Market & therapy area assessment
  • Emerging trends monitoring
  • Strategic reporting & visualization (dashboards, reports, presentations)

Evidence synthesis capabilities

From a complete review to a single task - built around your project

CliniWings supports pharmaceutical, biotechnology, medical technology, consultancy and research teams with structured literature reviews and evidence synthesis. Follow the three chapters below to see what we deliver and how you can work with us.

Chapter 01

Complete project capabilities

Commission a full review and we take it from research question to final report. Each offering is matched to a typical purpose and a defined set of deliverables.

01
The gold standard

Systematic literature review

Best forAnswer a defined clinical, economic or humanistic research question

7 main deliverables

  1. Protocol
  2. Reproducible searches
  3. Screening
  4. Extraction
  5. Appraisal
  6. Synthesis
  7. Report
02
Focused & efficient

Targeted literature review

Best forInform a focused decision using explicitly defined sources and limits

4 main deliverables

  1. Search approach
  2. Selected evidence
  3. Evidence tables
  4. Focused report
03
Time-sensitive

Rapid evidence review

Best forAnswer a time-sensitive question using agreed methodological adaptations

4 main deliverables

  1. Documented streamlined methods
  2. Evidence tables
  3. Findings
  4. Limitations
04
Map the landscape

Scoping review

Best forMap the range, characteristics and gaps in a body of literature

5 main deliverables

  1. Review framework
  2. Searches
  3. Selection
  4. Data charting
  5. Evidence map
05
Value evidence

Economic and outcomes review

Best forIdentify costs, HRU, HRQoL, utilities or economic evaluations

3 main deliverables

  1. Outcome-specific evidence tables
  2. Appraisal
  3. Synthesis
06
Find what is missing

Evidence gap assessment

Best forIdentify unanswered questions within a defined evidence landscape

3 main deliverables

  1. Evidence inventory
  2. Gap matrix
  3. Research implications
07
Keep it current

SLR update

Best forRefresh an existing systematic review

5 main deliverables

  1. Updated searches
  2. New studies
  3. Revised tables
  4. Flow diagram
  5. Synthesis
Refreshes review 01
Methods matched to purpose. Review methods are selected for the question and intended use. A targeted or rapid review is described transparently and is not represented as a full systematic review. Quantitative synthesis proceeds only when the evidence and assigned statistical expertise support it.

End-to-end delivery

The proposal defines responsibilities, review rounds, assumptions and acceptance criteria.

  1. Scope & feasibility
  2. Protocol
  3. Search
  4. Screening
  5. Extraction
  6. Appraisal
  7. Synthesis
  8. Reporting & handover
Chapter 02

Individual task capabilities

Engage us for one stage or a combination of tasks within your existing project. Every task has a clear scope and a defined deliverable that fits your protocol, templates and workflow.

Phase 1
Plan & search
4 tasks
TaskScopeDeliverable
Question and protocol
Research question, PICOS or other suitable framework, criteria and methods
Protocol or protocol amendment
Search development
Database-specific concepts, terms and limits; peer review where commissioned
Search strategies and rationale
Search execution
Agreed databases, trial registries and grey literature sources
Search logs and exported records
Reference preparation
Deduplication and preparation for screening
Clean library and reconciliation counts
Phase 2
Screen & retrieve
3 tasks
TaskScopeDeliverable
Title and abstract screening
Apply agreed eligibility criteria
Screening decisions and query log
Full text screening
Eligibility review and exclusion reasons
Included study list and exclusion log
Full text retrieval support
Locate articles through authorized routes
Retrieval tracker and unresolved requests
Phase 3
Extract & appraise
3 tasks
TaskScopeDeliverable
Data extraction
Design or use a piloted extraction template
Study and outcome evidence tables
Extraction verification
Check selected or all fields against source reports
Corrections and discrepancy log
Critical appraisal
Apply tools appropriate to design and review purpose
Risk of bias or appraisal tables
Phase 4
Synthesize, report & QC
4 tasks
TaskScopeDeliverable
Evidence synthesis
Summarize clinical, economic or humanistic findings
Narrative synthesis and comparison tables
Quantitative analysis
Feasibility and agreed statistical analysis
Analysis outputs, plots and interpretation
Reporting and figures
Methods, results, PRISMA flow and evidence summaries
Report sections and editable figures
Independent quality review
Review specified searches, decisions, data or outputs
QC findings and resolution tracker
How single tasks work. Single-task engagements require an approved protocol or written instructions. We agree how uncertainties are escalated, who resolves disagreements and how outputs are integrated into your project.
Chapter 03

Two ways to work with us

Commission a complete review, or engage us for a defined task within an existing project - and extend either into review updates or ongoing support.

Complete project

Way 1
What you commission

An agreed review from question development to final reporting

What you receive

Protocol, searches, screening decisions, evidence tables, appraisal, synthesis and report as scoped

Individual task

Way 2
What you commission

One stage or a combination of tasks within your project

What you receive

Defined outputs compatible with your protocol, templates and delivery workflow

Review update

Also available
What you commission

An update to an existing evidence base

What you receive

New searches, updated screening and extraction, and revised outputs

Ongoing support

Also available
What you commission

Scheduled literature updates or agreed research capacity

What you receive

Recurring deliverables and progress reporting under a defined statement of work

Quality built into every service

Deliverables aligned with recognised international standards, with reviewer roles, verification and senior scientific review agreed for every project.

  • PRISMA
  • ICH
  • GPP3
  • HTA

Ready to Elevate Your Evidence Strategy?

Partner with CliniWings for data-driven insights that support your most critical regulatory, clinical, and commercial decisions.

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