Services
World-class Expertise in Vascular Innovation
Founded by true experts in the vascular and clinical research space, KANDO Research specializes in delivering comprehensive research services tailored specifically to the needs of vascular medical device companies worldwide.
We offer a complete portfolio of research services — from specialized, strategic advisory services to full service projects. Our world-class insights and tailored approach ensure every phase of your project is managed efficiently, delivering high-quality results on time and within budget.
Advisory Services
Expert advice
regarding vascular product development and technology optimization such as technical design features, intended use, clinical practice feedback, etc.
Strategic navigation
of clinical and regulatory pathways.
Clinical program and study protocol design
including regulatory and medical writing.
Market access
and commercialization considerations.
Full Service Projects
Comprehensive Clinical Operations
Comprehensive clinical operations with full project management across all trial phases, efficient study startup, regulatory submissions, end-to-end site management including site identification, qualification, selection, initiation, monitoring and close-out, as well as full trial documentation management (TMF).
Regulatory and Medical Writing
Regulatory and Medical Writing for all regulatory and clinical documentation such as Clinical Evaluation Plan and Report (CEP/CER), systematic literature review and state-of-the-art (SLR/SOTA), Clinical Development Plan (CDP), post-market clinical follow-up and post-market surveillance (PMCF/PMS) plan and reports, Clinical Study Reports, etc.
Data Management
Data Management, eCRF design, randomization (IXRS), Patient reported outcomes (ePRO), eDiary.
Safety
Safety including safety plan development, medical monitoring and event adjudication and coding, event case processing and regulatory reporting, Data and Safety Monitoring Board (DSMB) and Clinical Events Committee (CEC).
Biostatistics
Biostatistics including sample size calculations, statistical analysis plan (SAP), randomization plan, TLF programming, SDTL and ADaM datasets, TLFs and interim and final statistical analysis report.
Corelab Management
Corelab Management including image transfer tools, image compliance and analysis.
Clinical Field Support
On-Site Procedural Expertise
Our Clinical Field Specialists provide hands‑on support during procedures, ensuring correct device use, protocol adherence and consistent execution across all participating sites. Their presence reduces variability and strengthens data quality.
Device Training & Competence Building
We train investigators, nurses and site staff in device handling, troubleshooting and workflow integration. This ensures every site operates confidently and safely from first‑patient‑in through study close‑out.
Consistent Study Execution Accross Sites
By standardizing device use and supporting site teams directly, we reduce inter‑site variability and help Sponsors achieve reproducible, high‑quality clinical outcomes.
Enrollment Boost
Field Support can meaningfully boost enrollment in endovascular medical device studies by giving investigators direct, on-site access to technical and procedural expertise exactly when it matters most. By supporting physicians in real time with device handling, procedural workflow, and patient screening against inclusion/exclusion criteria, Field Support lowers the barrier to enrolling a patient, while accelerating site proficiency through hands-on training and proctoring so sites enroll patients sooner and with more confidence.
Field Insights for Continuous Improvement
CFS professionals capture real‑world feedback from clinicians and sites, providing Sponsors with actionable insights to refine device usability, study procedures and future iterations.
Flexible Deployment Models
Whether you need full‑time field coverage, ad‑hoc support or rapid deployment for high‑stakes procedures, our network of trained specialists adapts to your study’s operational needs.
Global coverage
We bring our expertise to clients worldwide, ensuring seamless support across borders and time zones. Our tailored approach means that, wherever your study takes place, you’ll receive the same dedicated guidance, regulatory insight, and operational excellence we’re known for. With resources spanning continents, we combine local knowledge with global standards, helping you advance your technology with confidence — no matter the location.
