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GlobalReg Solutions

Orlando, United States (US) · Health and Medical

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Last verified

May 2026

GlobalReg Solutions is a leading regulatory consulting firm based in Orlando, Florida, specializing in quality and regulatory services for the medical device, pharmaceutical, and digital health industries.We support companies navigating the complex global regulatory landscape, assisting with FDA, EU MDR, Health Canada, and other international submissions.

Overview

GlobalReg Solutions is a leading regulatory consulting firm based in Orlando, Florida, specializing in quality and regulatory services for the medical device, pharmaceutical, and digital health industries.

We support companies navigating the complex global regulatory landscape, assisting with FDA, EU MDR, Health Canada, and other international submissions. Our team of experts guides clients through every stage, from initial strategy development to post-market compliance, ensuring efficient and compliant market access.

GlobalReg Solutions offers tailored solutions for startups and established companies, including regulatory pathway consulting, due diligence, QMS implementation, and risk management. We leverage our 25+ years of experience and 130+ successful global submissions to deliver confidence and accelerate your innovation. We are dedicated to helping you bring your medical devices and digital health solutions to patients worldwide.
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Contact Details

info@myglobalreg.com

Orlando, United States (US)

Founded

2022

Company Type

Sole Proprietorship

Employees

2-10

Categories

Medical Technology Solutions
Manufacturing
Medical Equipment and Services

Keywords

#samd validation

#supplier quality

#eo sterlization

#biocompatibility

#electrical safety test

#fda

#eumdr and international regulations

#medical device registration

#medical device classification

#regulatory strategy

#medical device quality management system

Awards

• 2026 OpenSee all

Services

Default Product Image
QMS Implementation Services
Medical Equipment and Services

We assist companies in implementing robust Quality Management Systems (QMS) aligned with ISO 13485, 21 CFR Part 820, and MDSAP standards, ensuring global market readiness and compliance.

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