Medical device consulting services

Uncovering the Impact of Endocrine Disrupting Substances in Biological Evaluation of Medical Devices

Medical device, Medical Device Consultancy, Medtech Consulting, Medical Device Consultant,

In recent years, there has been growing concern about the presence of endocrine-disrupting substances (EDS) in various products, including medical […]

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REPROCESSING OF REUSABLE MEDICAL DEVICES: INTRODUCTION

Medical device, Medical devices, Medical Device Consultant, Medical Device Consultancy,

Hello readers! We are launching another blog series on reprocessing of reusable medical devices. The idea is to serve you

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ARE YOU READY TO MOVE TO ELECTRONIC IFUs?

IFUs, Medical Devices, Medical Device Consultancy, Medical device consulting services,

Are you one of those who thinks uploading instructions for use (IFU) on the website is enough to meet the

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REPROCESSING OF REUSABLE MEDICAL DEVICES: WORST-CASE SELECTION

Medical Device Consultants in India, Medical device consulting service, Medical Device Consultancy,

All right, we’re back with more content on reprocessing of reusable medical devices. We introduced this topic in our last

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Clinical-evaluation-of-medical-devices-III

Medical Devices, Medical device consulting, Medical Device Consultancy, Medical Device Consultant,

Hello and welcome to another brainstorming blog to discuss the clinical evaluation of medical devices! In our previous blog post,

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An introduction to the IEC 60601 standard.

IEC 60601, Medical Device Consultant, Medtech Consultant , Medical Device Consultants in India,

Medical devices powered by electricity offer life-saving capabilities, yet they also present risks, especially when invasive procedures bypass the body’s

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eSTAR Program: Revolutionizing FDA Regulatory Process

estar, fda, estar program, Regulatory Affairs Consultants, Medical Device Regulatory Consulting,

In the ever-changing landscape of medical device regulation, technology plays a vital role in improving efficiency and ensuring robust processes.

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Best Practices for Selecting a Predicate Device to Support a Premarket Notification [510(k)] Submission

510 k, Medical Devices, Medical Device Consultants in India, Medical Device Regulatory Consulting,

USFDA (United States Food and Drug Administration) regulates medical devices in the USA. According to USFDA, medical devices are classified

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Applying Usability Engineering to Medical Devices

Medical Devices, Regulatory Consultant, Medical Device Regulatory Consultants in India,

Usability engineering for medical devices, or human factors engineering, is a concept of understanding interactions between the user and the

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Make-in-India forMedical Devices:Is there a support?

Medical devices, Medical Device Manufacturing Consultant, Medical device consulting services,

The previous blog on Make-in-India set an understanding for our readers about how the Indian medical devices market is growing,

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Clinical evaluation of Medical Device-Part II

Medical Device, Clinical Evaluation, CE for Medical Device, Medical device consulting services,

Welcome back, everyone! We hope your medical devices are performing well and meeting the necessary approval standards. If you require

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