Services | ResearchMedi
Our customized solutions adapt to your project’s needs; whether
you’re developing a new molecule, submitting to regulators, or
preparing for publication.
- Whether you’re a startup biotech or a multinational CRO, our flexible
and scalable services ensure you get the expertise you need. - From protocol design to regulatory submission, our cross-functional
team supports the entire research lifecycle.
Medical Writing Services
• Clinical Study Reports (CSR)
• Research proposals
• Investigator Brochures
• Patient case reports
• Manuscripts for peer-reviewed journals
• Regulatory and submission writing (IND, NDA, MAA)
• Conference abstracts and posters
• Scientific slide decks
• Medical education content
Biostatistics Services
• Statistical protocol development
• Trial design and sample size calculation
• SAS programming and reporting
• Data review and cleaning
• Interim analysis and final reporting
• Real-world evidence studies
• Advanced modeling and meta-analyses
• End-to-end statistical planning and analysis
• Data visualization and presentation
Consultation Services
• Pharma & Biotech
• Medical Device Manufacturers
• CROs
• Academic & Research Institutions
• Public Health Agencies
• Hospitals & Clinics
Onsite Services
Need hands-on expertise? Our specialists provide onsite or remote
support tailored to your trial timelines and operational needs.
"ResearchMedi’s expertise in medical writing and data analysis has been instrumental in the success of our clinical trials. Their team is professional and truly passionate about what they do."
"From protocol writing to stakeholder engagement, ResearchMedi has been a trusted partner in our journey to bring innovative treatments to market. Thanks for service and I highly recommend them f"
"ResearchMedi’s expertise in medical writing and data analysis has been instrumental in the success of our clinical trials. Their team is professional, reliable, and truly passionate about what they do."