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About Us

MedXCRO is a trusted partner in clinical research and CRO services, offering end-to-end solutions for pharmaceutical, biotech, and medical device companies

Contact Info

Learn How We Can Help

From study planning to regulatory compliance, MedXCRO delivers end-to-end solutions for successful clinical trials.

Your Trusted Partner in Clinical Research Excellence
Discover Our Expertise

Expert data management, biostatistics, and medical writing services ensuring accuracy and compliance.

Data-Driven Decisions for Better Outcomes
See Our Compliance Solutions

From IND/CTA submissions to GCP audits and IRB compliance, MedXCRO ensures your trials meet global standards.

Regulatory & Quality Assurance You Can Rely On
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What We Do

MedXCRO is the global development hub to support therapeutic innovators in the areas of neurovascular and peripheral products.

The MedXCRO team possesses a combined 35+ years of clinical, commercial, and regulatory experience in the development of these products. Their deep knowledge has put us at the forefront of new technologies as we work to aid patients by efficiently bringing leading-edge products to market.

Service Offering

Study Planning & Design
Protocol Development Feasibility Studies Statistical Consulting CMS Application
Regulatory Affairs
IND/CTA Submissions Ethics Committee Coordination Regulatory Strategy
Site Management
Site Selection & Initiation Site Monitoring
Site Closeout
Project Management
Study Startup Coordination Timeline & Budget Oversight
Risk Management
Clinical Operations
Investigator Meetings CRA Oversight
Patient Recruitment Strategies
Data Management
CRF Design
EDC Setup & Validation Data Cleaning & Query Management
Biostatistics
Statistical Analysis Plans (SAP)
Interim & Final Statistical Analysis
Medical Writing
Clinical Study Reports (CSR)
Investigator Brochures Informed Consent Forms
Scientific Journals Journal Submissions
Quality Assurance
GCP Audits
SOP Development Inspection Readiness
Training & Support
GCP Training
Protocol Training
Site Staff Support
E-Learning Modules
Creation of training modules
Social Media
Social Media Posting

Clinical Excellence in Medical Devices & IVDs

Evidence-Based Design & Validation

Clinical excellence begins with devices and diagnostics being developed and validated through rigorous clinical studies. This ensures accuracy, reliability, and real-world effectiveness across diverse patient populations.

Compliance with Global Regulatory Standards

Adhering to standards such as FDA (USA), CE (Europe), or CDSCO (India) ensures that devices and IVDs meet the highest safety and performance benchmarks, supporting better clinical outcomes.

Continuous Post-Market Surveillance & Innovation

High-performing companies prioritize continuous monitoring and feedback from healthcare professionals, enabling ongoing improvements, faster diagnostics, and more personalized patient care.

Key Therapeutic Areas

We have in-depth expertise in the challenges associated with medical devices and In Vitro Diagnostics, with a focus on cardiology, vascular, neurology, and orthopedics.

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MedxCRO

Your Trusted Clinical Research Partner

We’re here to support your clinical and regulatory needs with tailored solutions. Get in touch with MedXCRO to discuss how we can drive your research forward.

Service Recipient Says

Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious.

Kolis Muller NY Citizen

Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious.

Kolis Muller NY Citizen

Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious.

Kolis Muller NY Citizen

Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious.

Kolis Muller NY Citizen

News & Blog

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