CliniWings Evidence Consultancy
Evidence that drives better patient outcomes
Specialists in Real-World Evidence, Systematic Literature Reviews, HEOR and Medical Writing
Providing RWE, SLR and HEOR solutions that drive innovation, value and better patient outcomes, from real-world evidence to strategic insights for research, publications and healthcare decision-making.
- PRISMA · ICH · GPP3 aligned
- Complete projects or single tasks
- Hyderabad, India
Evidence synthesis workflow
From research question to decision-ready evidence
Welcome to CliniWings
Reliable, data-driven insights for healthcare decisions
CliniWings Evidence Consultancy partners with pharmaceutical, biotechnology, and healthcare organizations to deliver reliable, data-driven insights. We specialize in Real-World Evidence (RWE), Systematic Literature Reviews (SLR), Health Economics & Outcomes Research (HEOR), and medical writing, supporting decisions across clinical development, regulatory processes, and market access.
We transform complex data into clear, actionable insights through a blend of scientific expertise and advanced analytics. From early research to post-marketing and publication support, we provide end-to-end evidence solutions with a strong focus on accuracy, compliance, and strategic value.
Our services
Built on Expertise. Driven by Results.
End-to-end solutions for research, publications, and healthcare decision-making.
Real-World Evidence (RWE)
Evidence from claims, EHRs, registries and patient-reported outcomes to show how therapies perform in real clinical settings.
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Systematic Literature Review (SLR)
Comprehensive, reproducible, PRISMA-compliant reviews and evidence synthesis for regulatory, clinical and market access decisions.
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Health Economics & Outcomes Research (HEOR)
Economic modelling, outcomes assessment and cost analysis to support market access and reimbursement.
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Medical & Scientific Writing
Clear, compliant regulatory documents, manuscripts and value dossiers that translate science into action.
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Publication & Research Support
End-to-end support to plan, prepare and publish your research for maximum visibility and impact.
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Competitive Intelligence & Landscape Analysis
Insights into therapeutic areas, competitor activity and market trends to keep you ahead.
Learn moreEvidence synthesis
Evidence to support your research decisions
We support pharmaceutical, biotechnology, medical technology, consultancy and research teams with structured literature reviews and evidence synthesis. We define the research question, build a reproducible evidence base and present findings in clear, usable deliverables.
Commission a complete review, or only the task you need
Two ways to work with us, from a full project to a defined stage within your existing workflow.
Complete project
An agreed review from question development to final reporting.
Individual task
One stage or a combination of tasks within your project.
Review update
An update to an existing evidence base.
Ongoing support
Scheduled literature updates or agreed research capacity.
Complete project capabilities
The right review for your question
Select a review type to see its typical purpose and main deliverables.
01
Systematic literature review
Answer a defined clinical, economic or humanistic research question.
Main deliverables
- Protocol
- Reproducible searches
- Screening
- Extraction
- Appraisal
- Synthesis
- Report
02
Targeted literature review
Inform a focused decision using explicitly defined sources and limits.
Main deliverables
- Search approach
- Selected evidence
- Evidence tables
- Focused report
03
Rapid evidence review
Answer a time-sensitive question using agreed methodological adaptations.
Main deliverables
- Documented streamlined methods
- Evidence tables
- Findings
- Limitations
04
Scoping review
Map the range, characteristics and gaps in a body of literature.
Main deliverables
- Review framework
- Searches
- Selection
- Data charting
- Evidence map
05
Economic and outcomes review
Identify costs, HRU, HRQoL, utilities or economic evaluations.
Main deliverables
- Outcome-specific evidence tables
- Appraisal
- Synthesis
06
Evidence gap assessment
Identify unanswered questions within a defined evidence landscape.
Main deliverables
- Evidence inventory
- Gap matrix
- Research implications
07
SLR update
Refresh an existing systematic review.
Main deliverables
- Updated searches
- New studies
- Revised tables
- Flow diagram
- Synthesis
End-to-end delivery
From scoping question to final handover
A clear, traceable path through every stage of your review. The proposal defines responsibilities, review rounds, assumptions and acceptance criteria.
- 01
Scope & feasibility
Question, intended use and feasibility
- 02
Protocol
PICOS framework, criteria and methods
- 03
Search
Databases, registries and grey literature
- 04
Screening
Title, abstract and full-text eligibility
- 05
Extraction
Piloted templates and evidence tables
- 06
Appraisal
Risk of bias and quality tools
- 07
Synthesis
Clinical, economic and humanistic findings
- 08
Reporting & handover
PRISMA flow, report and editable figures
Have a research question in mind? We assess scope, feasibility, resource needs and dependencies before work begins.
Plan & search
Frame the question and build a reproducible search.
Screen & retrieve
Apply eligibility criteria and secure full texts.
Extract & appraise
Capture the data and judge study quality.
Synthesize, report & QC
Turn evidence into findings, figures and checked outputs.
Why CliniWings?
A team that prioritizes quality, precision, and results
Scientific expertise, advanced analytics and a client-focused approach - delivering reliable evidence at every step.
Scientific Expertise
Deep knowledge in epidemiology, biostatistics, and health economics ensuring reliable, credible evidence at every step.
Integrated Service Model
Complete range from RWE and SLR to HEOR and medical writing - seamless end-to-end project execution.
Advanced Analytics & RWD
Work with diverse healthcare datasets - claims, EHRs, and registries - to generate meaningful, actionable insights.
Regulatory Compliance
Deliverables aligned with PRISMA, global regulatory standards, and HTA requirements.
Broad Therapeutic Coverage
Expertise spanning oncology, cardiovascular, neurology, infectious diseases, rare conditions, and beyond.
Client-Focused Approach
Every project tailored to specific client needs - ensuring timely delivery and consistently high-quality outcomes.
Deliverables aligned with global standards
- PRISMA
- ICH
- GPP3
- HTA
Therapeutic areas
Comprehensive Expertise Across Every Domain
Multidisciplinary expertise across a broad range of therapeutic areas, supporting informed clinical and commercial decisions globally.
View all therapeutic areasHEOR evidence & scientific outputs
Evidence across clinical, economic and humanistic outcomes
Our services help teams understand treatment outcomes, disease burden, healthcare resource use, quality of life and published economic evidence.
Clinical evidence
- Efficacy, effectiveness and safety outcomes across defined interventions and populations
- Subgroup and special-population evidence, where available
Economic and humanistic evidence
- Cost of illness, healthcare resource utilization and direct or indirect costs
- HRQoL, patient-reported outcomes and health-state utilities
- Published cost-effectiveness, cost-utility and budget impact evaluations
- Identification and appraisal of economic model inputs
Epidemiology
- Disease incidence and prevalence
- Disease burden and unmet needs reported in published studies
Treatment patterns
- Evidence on treatment patterns across defined populations and settings
Natural history
- Evidence on disease prognosis and progression
Reports and publication support
- Technical reports, evidence tables and executive summaries
- Manuscripts, abstracts, conference posters and presentation content
Authorship, journal requirements, review rounds and submission responsibilities are agreed separately; publication acceptance is not guaranteed.
Scientific leadership
Naresh Goli
Founder & DirectorScientific leadership is provided by Naresh Goli, with an M.S. in Pharmacology and Toxicology from NIPER and experience in evidence synthesis and HEOR. His previous professional experience includes BresMed/Lumanity and ICON plc.
- M.S. Pharmacology & Toxicology, NIPER
- Evidence synthesis
- HEOR
Who we support
Built for teams across the healthcare ecosystem
- HEOR and market access consultancies
- Pharmaceutical and biotechnology companies
- Medical technology companies
- Contract research organizations (CROs)
- Medical communications agencies
- Hospitals
- Academic and independent research teams
Client Testimonials
What Our Clients Say About Us
Feedback from pharmaceutical, biotech and research partners we have supported with evidence, analytics and writing.
CliniWings delivered a comprehensive RWE study that significantly strengthened our regulatory submission. Their analytical expertise is impressive.
Their systematic literature review was detailed, accurate, and perfectly aligned with PRISMA guidelines. Highly recommended.
The HEOR modeling provided by CliniWings played a key role in our successful market access strategy.
Professional medical writing services with excellent clarity and compliance. Our manuscript was accepted without major revisions.
Project controls
Quality, confidentiality and clear terms, agreed up front
Every engagement runs under a defined statement of work, so you know exactly who does what, how it is checked and what you receive.
An agreed quality approach
Reviewer roles, verification coverage, disagreement resolution, senior scientific review and deliverable acceptance are specified for each project. Dual independent screening or extraction is included when the agreed methodology requires it.
Confidentiality and access
Confidentiality terms, authorized access, permitted software, file exchange, retention and deletion requirements are agreed before work begins.
Pricing and timelines
Complete projects and defined tasks can be quoted at a fixed fee once scope is clear. Ongoing support can use an agreed capacity or retainer arrangement.
How an engagement starts
Five simple steps from first conversation to project kick-off.
- 01Share your question, intended use, population, interventions, outcomes and deadline.
- 02Provide any existing protocol, search, library, template or completed outputs.
- 03We assess scope, feasibility, resource needs and dependencies.
- 04Agree a proposal covering deliverables, milestones, fees, QC and review rounds.
- 05Begin work with scheduled updates, escalation routes and documented handover.
Ready to begin
Working on an evidence review, a model, or a publication?
Share your requirement and our team will get back to you with the right next steps.
Tell us about your projectWhat services does CliniWings provide?
CliniWings offers a wide range of services including Real-World Evidence (RWE), Systematic Literature Reviews (SLR), HEOR, medical writing, publication support, and competitive intelligence.
Who can benefit from your services?
Pharmaceutical and biotechnology companies, medical device manufacturers, healthcare and consulting organisations, and academic and research teams that need reliable, data-driven evidence.
Do you offer customized project solutions?
Yes. Every project is tailored to your objectives, therapeutic area, target markets and timelines.
Are your deliverables compliant with global standards?
Yes. Our work follows recognised standards such as PRISMA, ICH and GPP3 guidelines, and HTA requirements.
Can you support projects from start to finish?
Yes. We support projects end to end - from protocol and study design to analysis, reporting, publication and submission support.
Ready to Elevate Your Evidence Strategy?
Partner with CliniWings for data-driven insights that support your most critical regulatory, clinical, and commercial decisions.