Toolkit for Medical Device Registration by Startups
Here is a high level summary of how startups can plan their product development and commercialization for new medtech innovations/ideas.
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Navigate the MedTech Odyssey From Idea to Impact
Services
Post Marketing Surveillance
Market Access & Marketing
Product Development
Regulatory Affairs
Quality Management
Clinical Services
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Artixio helps Medical Devices & Diagnostics Companies deliver meaningful global impact through MedTech InnovateIO platform, right from the Product Development and Post Market Lifecycle.
Discover stories that inspire from the best in the industry - from established MedTech Leaders, new-age Individual Innovators to well-known
Academic and Research Organizations.
Our Pillars
Provide access to important learning programs specially designed for current and future MedTech professionals. Learn from industry experts and academic professionals everything from concept to commercialization.
Our Pillars
Identify and support upcoming MedTech Innovations, from the world of academia or solo entrepreneurs looking to make it big using our Innovation Grants and Mentorship.
Our Pillars
Become a long-term supportive partner with MedTech Innovators through Expert Consulting, Services and Solutions across the MedTech product lifecycle.
Our Pillars
We are proud members of
Your MedTech Partner, from Concept to Market
The journey from concept to market is not a short one. Our team of global experts work toward helping your MedTech idea achieve safe commercialization while ensuring reduced time to market.
100+
Products Registered
40+
Device Technology Categories
20+
Products Developed
15+
Years of Experience
At a glance
Our Services
Our suite of comprehensive solutions guides you at every stage of the MedTech journey. Whatever your involvement may be, our services are customized to your specific needs. To know more, check them out below.
Regulatory Affairs
Regulatory Intelligence & Strategy, Gap Analysis, Remediation and Submission
Quality Management
QMS Implementation
ISO 13845 Consulting, 21 CFR
820, SOP Development, Audits
Clinical Services
Clinical evaluation reports (MEDDEV 2.7.1)
Clinical investigation protocols and reports
Medical Writing & Medical Review
Post Marketing Surveillance
Customer Complaints collation
Medical Device Reporting
Unsolicited User Feedback
Maintenance / Service Reports
Device Misuse / Compatibility Issues PMS Plan
Vigilance & Post Market Safety Reports(PMSR)
Periodic Safety Update Report (PSUR)Services
MDR reporting- 3500A Form
Market Access
Market Size & Landscape Analysis
KOL Analysis
Price Sensitivity Analysis
Distributor Search and Licensing
Product Development
Medical Device Prototyping
Hybrid Application Development
Data Science & Analytics
Machine Learning
Internet of Things
200+ Experts Across
70+ Countries
From Registration and Holding Licenses to Import Assistance and Distribution Support, we help you achieve global commercialization with our worldwide presence.
Make your Mark in the MedTech Sector
Our annual grant for Early Stage MedTech Innovators fosters new innovations in an effort to extend our commitment to the MedTech community. Unlock a golden opportunity to take your MedTech idea global with us.
MedTech InnovateIO –
The Podcast
Get inspired by stories of MedTech Leaders and Innovators from around the world. Join our founders in hearing how they stumbled upon the idea, developed successful products, the grind, the glory - all of it and more.
Focused, In-depth Insights from Leading Industry Experts
Comprehensive MedTech Courses to Help You Stay Relevant
Irrespective of where you are in your MedTech journey, learn from our wide range of training modules built to suit your needs. Whether it be Innovators, Regulatory Professionals, Executive Management or Students, we have programs for everyone.
Building a Future in Health Technology
5 Days
Free
Empowering the future healthcare
5 Days
Free
Notified bodies
Risk management
Clinical Evaluation
Post-market surveillance
UDI
The Medical Device Regulation (MDR)
The In Vitro Diagnostic Medical Device Regulation (IVDR)
ISO 13485:2016
Explore Our Global
Technology Experience
With extensive product experience across various categories, we help you infuse the right technologies that bring your MedTech idea to life.
Active Implantable Medical Devices
Mobile devices
Diagnostics
Vascular
SaMD
Combination Device
Ophthalmology
Orthopedic
Others
“I do appreciate the
responsiveness, commitment and timely deliveries.”
Radhika Nathany
Founder, Skon Naturals
“I do appreciate the
responsiveness, commitment and timely deliveries.”
Radhika Nathany
Founder, Skon Naturals
“I do appreciate the
responsiveness, commitment and timely deliveries.”
Radhika Nathany
Founder, Skon Naturals
Testimonial
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