FAQ'S

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.