S-Cube Technologies

In a world where healthcare is evolving at an unprecedented pace, the design and development of medical devices demand meticulous attention to detail. The European Union’s Medical Device Regulation (EU MDR) 2017/745 has set new standards for the industry, requiring manufacturers to adhere to a systematic approach that ensures safety, efficacy, and compliance. In this guide, we’ll walk you through the steps of designing and developing a medical device under the EU MDR using the Waterfall process. We’ll also introduce you to SmartEye, an advanced eQMS software that can revolutionize your product lifecycle management.

Streamlining Medical Device Design and Development Under EU MDR 2017/745: A Comprehensive Guide - S-Cube Technologies In a world where healthcare is evolving at an unprecedented pace, the design and development of medical devices demand meticulous attention to detail. The European Union’s […]

Moving to an e-QMS (electronic QMS) solution shall help you with the documentation control, since many of the steps would be automatized and you would need to focus on what really matters rather than caring about versions, changes in the documents, reviews and updates. Your time spent on document control activities will decrease and therefore your document control will be efficient and successful.


https://scube-technologies.com/e-qms/documentation-control-in-iso-13485/

Documentation control in ISO 13485 - S-Cube Moving to an e-QMS (electronic QMS) solution shall help you with the

If you decide to purchase an on-line solution, ensure that is it a reliable company that will make your business not only to comply with the requirements of the standard but to grow and be more competitive in the market.


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https://scube-technologies.com/e-qms/advantages-and-disadvantages-of-e-qms-in-medical-device-companies/

Advantages and disadvantages of e-QMS in medical device companies - S-Cube The release of software tools, such as e-QMS (electronic Quality Management System), has undoubtedly marked a before and after in the implementation and maintaining of international standards, and especially in the part of document and record control.

We’re proud to announce you our new project eQMS SmartEye.

S-Cube SmartEye is ready for your next audit inspection, before you even know it’s happeningeQMS SmartEye.

S-Cube SmartEye is ready for your next audit inspection, before you even know it’s happening


Arrange your free tailored demo of S-Cube SmartEye today, and see for yourself how an enhanced 360 view could benefit your SaMD design and development.
www.scube-technologies.com

https://podcast.easymedicaldevice.com/182/?mc_cid=d667ca518a&mc_eid=d4147d6094

Let's introduce you to our eQMS SmartEye with Anindya Mookerjea Medical Device made Easy Podcast episode on eQMS SmartEye with Anindya Mookerjea CEO of S-Cube Technologies

It's now easier to contact S-Cube Technologies.