Medical Research
Support Services
Supporting clinicians, institutions, and organizations across the entire medical research lifecycle — from study concept to publication.
Medforage provides end-to-end medical research support with a strong focus on scientific accuracy, ethical compliance, and publication-ready quality.
Our Medical Research Services
1. Research Concept & Study Design Support
- Research idea refinement and feasibility assessment
- Study design (observational, interventional, retrospective, prospective)
- Protocol framework development
- Endpoint and outcome measure selection
- Sample size rationale support (non-statistical)
2. Clinical Research Protocol Development
- Detailed clinical study protocol writing
- Study objectives, methodology, and timelines
- Inclusion & exclusion criteria drafting
- Data collection and visit schedule planning
3.Ethics Committee & Regulatory Documentatin
- IEC / IRB submission documentation support
- Informed consent form (ICF) drafting (patient-friendly language)
- Participant information sheets
- Regulatory checklists and submission assistance
- Response support for ethics committee queries
4.Medical Writing & Scientific Documentation
- Clinical study reports (CSR)
- Investigator brochures (IB)
- Case report narratives
- Scientific summaries and white papers
- Medical education content based on research outcomes
5.Manuscript Writing Journal
Publication Support
- Original article writing
- Review articles & systematic reviews
- Case reports & case series
- Journal selection and formatting
- Submission-ready manuscripts as per journal guidelines
6. Abstract, Poster & Oral Presentation Support
- Scientific abstract writing and editing
- Poster design and content structuring
- Oral presentation (PPT) development
- Conference submission compliance support
- Visual data storytelling for medical audiences
7.Data Review, Interpretation & Research Insights
- Data cleaning and consistency checks (non-statistical)
- Clinical interpretation of results
- Literature-based contextual analysis
- Outcome narrative development
- Scientific insight generation for presentations & publications
8. Systematic Reviews & Evidence Synthesis
- Systematic and narrative literature reviews
- PRISMA-aligned review structuring
- Evidence mapping and gap analysis
- Meta-analysis coordination support (with statisticians)
- Real-world evidence (RWE) summaries
9. Publication Ethics & Authorship Compliance
- ICMJE authorship guidance
- Plagiarism checks and originality review
- Conflict of interest documentation
- Transparency and disclosure compliance
- Ethical publication practices advisory
10. Pharma & Industry Research Support
- Investigator-initiated study (IIS) documentation
- Post-marketing study (PMS) support
- Real-world evidence (RWE) documentation
- Scientific communication for pharma-sponsored research
11. Academic & Institutional Research Support
- Thesis and dissertation writing assistance
- Faculty research documentation
- Medical college research support
- Academic journal submission assistance
- Research mentoring documentation
12.Conference & CME Research Support
- Scientific content for CMEs
- Research-based session planning
- Speaker notes and discussion guides
- Live case documentation and summaries
- Post-conference research publications
13.AI-Enabled & Technology-Assisted Research Support
- Literature screening acceleration
- Reference management and citation accuracy
- Research workflow optimization
- Data visualization and figure creation
- Secure document collaboration systems
14.End-to-End Research Project Management
- Research timelines and milestone tracking
- Multi-stakeholder coordination
- Version control and documentation governance
- Confidentiality and data security management
- Final submission and archive support
