Global CRO
Partner in Neuroscience

Driving innovation in neurovascular and peripheral therapies with specialized clinical expertise.

Discover Our Expertise

Specialized. Fast
Agile. Trusted.

100% neuroscience-focused with proven excellence in trial startup, regulatory expertise, and global operations.

Explore Our Services

Success Delivered
Globally

From the U.S. to Europe and beyond — MedXCRO powers some of the fastest-enrolling neurovascular trials worldwide.

See Our Impact

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+1(978)-MED-XCRO

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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.

We are a specialized Contract Research
Organization fully dedicated to
neuroscience, with deep expertise in
neurovascular clinical trials.

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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

Why MEDXCRO

100% Neuroscience focused

Specialized in neurovascular trials

Flexible & Tailored Execution

Quick & Lean Operations

OUR VALUE PROPOSITION

High-Quality – Fast – Agile - Cost-Effective

Strong data quality
Regulatory expertise
Rapid trial startup & enrollment
Medical writing
Statistical Support
Competitive pricing

Connect with

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.

WHO ARE WE?

Laila Ibrahim

Director of Clinical Affairs

Stacy Parlette

Clinical Study Specialist

Linkildn

Samantha Turinsky

Clinical Research Specialist

Alyssa Axe

Clinical Research Manager

How it works

Our All-in-One CRO solution delivers the full package of CRO services, site operations and technology necessary to operate a study, beginning with building your protocol through to delivering your data.

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End-to-End

Run your trial with one partner, instead of going through the pain of stitching together multiple solutions. From design and recruitment, to data collection and delivery, we’ll be by your side from start to finish.

An Expert Team

We provide a clinical operations team consistently ranked based in industry for responsiveness and quality of execution who are assigned to your team based on extensive experience relevant to your trial.

Tech-Enabled

And to make everything even smoother, our end-to-end technology platform covers all your clinical software and tool needs. Our technology supercharges studies to deliver faster study startups and recruitment timelines.

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Contact Us

+1(978)-MED-XCRO

MedXCRO is a trusted partner in clinical research and CRO services, offering end-to-end solutions for pharmaceutical, biotech, and medical device companies. From study planning and regulatory affairs to site management, clinical operations, data management, and biostatistics, we ensure seamless execution and compliance at every stage. Our expert team also supports medical writing, quality assurance, training, e-learning, social media management, and CORE lab oversight to help clients achieve accurate, timely, and high-quality results.