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About us

About Us

  • At Medfins International, we are dedicated to simplifying the complexities of medical device compliance so that healthcare innovators can focus on delivering better patient outcomes. As a leading regulatory consultancy, we provide end-to-end support for medical device manufacturers, importers, and distributors seeking to achieve national and international approvals — including CDSCO licenses, CE marking, ISO certifications, and other critical regulatory milestones.
  • Since our founding, Medfins has been committed to bridging the gap between innovation and compliance. We combine deep regulatory expertise with a client-first approach, ensuring every project is handled with precision, transparency, and a genuine commitment to success. From start-ups launching their first device to global companies expanding into new markets, Medfins is your trusted partner in navigating the regulatory landscape.

Welcome to Medfins

Your trusted partner for medical device regulatory solutions. Let’s work together to ensure compliance, safety, and success across global markets.

Our Mission

To empower medical device companies by providing reliable, efficient, and ethical regulatory solutions that accelerate time to market, ensure compliance, and uphold the highest standards of patient safety.

Our Vision

To become a globally recognized leader in medical device regulatory consulting, known for driving innovation, ensuring safety, and fostering lasting partnerships across the healthcare ecosystem.

Our Core value

Integrity

We operate with honesty, transparency, and accountability in every engagement.

Innovation

We continuously update our knowledge and processes to stay ahead in a dynamic regulatory environment.

Responsiveness

We act swiftly and effectively, ensuring timely solutions that keep your projects on track.

Excellence

We strive for precision and quality in all our services, no matter how complex the task.

Collaboration

We work closely with our clients, understanding their challenges and delivering tailored solutions.

Customer-Centricity

Your success is our success. We treat your goals as our own.

What We Do

Regulatory Consulting

CDSCO medical device and IVD approvals, Import and Manufacturing licenses (Form MD-14/15, MD-9/10), CE certification, EU MDR / IVDR compliance, US FDA support.

Quality Systems & Certifications

ISO 13485, ISO 9001, risk management, technical file / dossier preparation.

Post-Market Services

Clinical evaluation reports, post-market surveillance, vigilance reporting.

Training & Advisory

Workshops and customized training sessions on regulatory requirements and quality systems.

Why Choose Medfins?

  • Global Regulatory Expertise – We help you navigate CDSCO, CE, ISO, US FDA, and more.
  • End-to-End Solutions – From product classification to certification and post-market compliance.
  • Time-Efficient Processes, – Fast-track approvals without compromising quality.
  • Cost-Effective & Transparent – No hidden charges, no surprises.
  • Dedicated Team – Our experienced consultants act as an extension of your in-house team.

Get the care you deserve

With our expertise and commitment, you can expect exceptional support for all your regulatory compliance needs.
How this works?
  • Fill out the registration form
  • Schedule a consultation
  • Meet with our regulatory expert
  • Receive tailored guidance
  • Make payment online or via invoice
  • Your project will be initiated by our Executive team

Schedule a Consultation