India’s 1st eQMS designed for global Medtech Industry

Smart Quality Management System for Medical Device Companies

Switch to easyQ eQMS: a next-generation, cloud based quality management system Software designed specifically for the medical device industry.

A complete solution that helps you stay compliant, work faster, and grow your business with confidence.

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From startup to scale-up: Business
smart QMS software designed to scale faster

At easyQ Solutions, we understand the pressure Indian Medical Device companies face starting from tight deadlines to rigorous compliance and limited resources which is why we have built easyQ eQMS: a platform designed specifically to assist you in complying with CDSCO while aligning with ISO 13485, FDA, and EU MDR making compliance local and global, effortless and scalable.

100%

Audit Ready

  • It speeds up quality operations by automating everyday compliance tasks
  • It keeps you always audit-ready, with real-time traceability and version control
  • Reduces operational workload so that your team can focus on innovation

Our Product Capabilities

Scale Smarter, Faster and Fully Compliant
Everything You Need in One Powerful eQMS

At easyQ Solutions, we have built easyQ eQMS as a modern, cloud-based system tailored for fast growing Medical Device companies. From startups to global manufacturers, our eQMS simplifies compliance with ISO 13485, 21 CFR Parts 820 and Part 11, EU MDR/IVDR, CDSCO and more.
It is easy to implement and scale with in-built workflows aligned to global standards.

Our QMS software focuses on:

Scalability for every stage: From Startups to Enterprises

Whether you are entering your first medical device into the market or managing complex global operations, our eQMS adapts to your scale and speed.

Smart & Collaborative Control

From Document Management to Complain Management, our eQMS brings your entire team together in one platform. You can assign, track, review, and sign off with complete traceability.

Compliance with Ease

Our eQMS is built with a simple interface, intuitive workflows, and fast onboarding. It is a modern, cloud-based QMS that works from day one

Measurable Outcomes

Transform How Your Team Works, Tracks, and Delivers

Fast-growing Medical Device teams don’t have time to chase paperwork, fix audit gaps, or second-guess compliance steps.

easyQ eQMS helps you shift from reactive to proactive quality management enabling your team to be efficient, stay compliant, and focus on innovation.

Instead of spending weeks on chasing approvals, fixing document errors, or preparing for audits , your team can now work smarter, faster and efficiently

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100%

Audit Ready

60%

Operation Cost Reduction

50%

Time Reduction

60%

Setup Effort Reduction

Results:
  • Enhances operational
    efficiency     50% - Reduction in Operational Efforts
  • Ensures compliance with full traceability 100% - Audit Ready
  • Accelerates time to market for innovation 60% - Reduction in operational cost & time
  • Lowers compliance
    costs     60% - Reduction in setup and maintanence

our clients

Trusted by Medtech Leaders Globally

Compliance assured

Our QMS Software Empowers Clients to align with

Compliance assuredCompliance assured

our certifications

Our QMS Software Platform Empowers Clients to align with

Effortless Compliance in a Constantly Evolving MedTech Landscape

testimonials

Hear from our Global Leaders

Strong regulatory support from easyQ Solutions enabled key compliance wins across India and global markets.

DR
Dr Rebecca Funston

Senior Director, Fourth Frontier, India

Thank you for making our ISO 13485 certification and manufacturing license process seamless and successful.

MA
M.R. Abinaya

AVP of Learning & Development, FITTERFLY, India

Trusted advisors and true partners in managing Crely’s Quality Management and Regulatory Affairs.

AS
Arun Sethuraman

Founder & CEO,  Crely Healthcare, Singapore

Thank you for the expert guidance in FDA submissions and QMS

DS
Dr. Swati Shukla

COO, Serigen Mediproducts Pvt Ltd

Grateful  for assisting us in obtaining FDA approval.

RJ
Rasiah Jegathes

President,  EDONORSOFT LLC, USA

Has been an invaluable partner in  ISO 13485 and CE marking journey

SV
Suthirth Vaidya

CEO, Predible Health, India

Thank you for supporting us in our QMS journey. Highly recommended!

JE
Javier Echenique

CEO, GPX Global Systems Inc, USA

Thanks to easyQ Solutions, we achieved ISO 13485 compliance with clarity and precision.

NR
N Ravi

CEO, Biocliq, India

easyQ Solutions was key to building and implementing our QMS successfully.

LE
Laina Emmanuel

CEO, Brainsight, India

latest Articles

Stay Updated with Our Latest Articles

Keep up with the latest trends, tips, and insights in our industry by reading our newest blog posts. From expert advice to company updates, our posts are designed to inform, inspire.

Difference between DHF, DMR and DHR

Difference between DHF, DMR and DHR

Download Article
FDA’s QMSR

FDA’s QMSR

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When to submit 510(k) for a software change to an existing device

When to submit 510(k) for a software change to an existing device

Download Article

Frequently Asked Questions (FAQs)

Got Questions? We've got Answers!

Whether you're curious about features, pricing, or getting started, we've got you covered. If you don't find what you're looking for, our team is always ready to assist you.

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Yes, easyQ Solutions offers complete data security. Using state of the art framework to keep your data safe and secured. The solution is compliant to 21 CFR Part 11

easyQ Solutions eQMS is built specifically for the Medical Device, it is aligned to meet requirements of ISO 13485 and 21 CFR Part 820. The built in feature ensures you stay compliant throughout your journey.

Yes, without a doubt. Regardless of whether your current QMS is paper-based or another digital system, our experts at easyQ Solutions offers comprehensive support for a smooth transition. To guarantee a seamless transition without interfering with your business operations, we assist with data mapping, validation, and onboarding.

Of course! easyQ Solutions houses QMS and Regulatory experts who can hand hold you through your journey. Right from conducting Audits to DHF remediations we are your partner to get it done.

The onboarding process typically takes two week, depending on the primary use case and focus areas defined by each customer.

No, never! easyQ Solutions is a cloud-based platform built on a modern technology stack, we will frequently offer updates and new features that are specifically designed to meet the demands of medical device manufacturers. We will ensure you are always complaint. We offer validation reports that can be utilized by you.

Yes!

easyQ Solutions is designed to help medical device companies comply with global regulations. Our eQMS is designed to meet global market regulations, such as ISO 13485, 21 CFR Part 820, and other regional standards.

Our software guarantees smooth operations across markets and helps to streamline compliance, regardless of whether you are based abroad or intend to grow internationally.

The tool currently offers modules such as Document Management, Risk Management, CAPA, Training, Complaint Management, MRM and more. As new features and modules keep getting built and upgraded, the same shall be provided to all our customers.

Your Compliance Journey Begins in One Click

Book your demo today and experience smart eQMS designed around your MedTech business to be compliant

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