Medtech Consultant - Alceon Medtech Consulting

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 […]

REPROCESSING OF REUSABLE MEDICAL DEVICES: INTRODUCTION Read More »

UncategorizedMedical device, Medical Device Consultancy, Medical Device Consultant, Medical device consulting services, Medical Device Manufacturing Consultant, Medical Device Regulatory Consulting, medical devices, Medtech Consultant

ARE YOU READY TO MOVE TO ELECTRONIC IFUs?

Uncategorized / December 17, 2024 / atonu dutta / IFUs, Medical Device Consultancy, Medical device consulting in India, Medical device consulting services, Medical Device Manufacturing Consultant, Medical Device Regulatory Consulting, medical devices, Medtech Consultant

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

ARE YOU READY TO MOVE TO ELECTRONIC IFUs? Read More »

UncategorizedIFUs, Medical Device Consultancy, Medical device consulting in India, Medical device consulting services, Medical Device Manufacturing Consultant, Medical Device Regulatory Consulting, medical devices, Medtech Consultant

An introduction to the IEC 60601 standard.

Uncategorized / December 16, 2024 / atonu dutta / IEC 60601, Medical Device Consultant, Medical Device Consultants in India, Medical device consulting services, Medical Device Manufacturing Consultant, Medical Device Regulatory Consulting, Medtech Consultant

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

An introduction to the IEC 60601 standard. Read More »

UncategorizedIEC 60601, Medical Device Consultant, Medical Device Consultants in India, Medical device consulting services, Medical Device Manufacturing Consultant, Medical Device Regulatory Consulting, Medtech Consultant

How to write an intended use for a medical device?

Uncategorized / December 16, 2024 / sanikakulkarni / FDA guidelines for medical devices, FDA Regulatory Consulting Firms, Medical device, Medical Device Consultancy, Medical Device Consultant, Medical device consulting companies in India, Medical device intended use, Medical Device Regulatory Consultants in India, Medical Device Regulatory Consulting, Medtech Consultant

Medical Device, FDA Regulatory Consulting Firms, Medtech Consultants, Medical Device Consultants,

Hello readers, we’re back with another topic in the series of Usability Engineering for Medical Device. The last blog described

How to write an intended use for a medical device? Read More »

UncategorizedFDA guidelines for medical devices, FDA Regulatory Consulting Firms, Medical device, Medical Device Consultancy, Medical Device Consultant, Medical device consulting companies in India, Medical device intended use, Medical Device Regulatory Consultants in India, Medical Device Regulatory Consulting, Medtech Consultant

Medical Device Usability Engineering: Using Specifications

Uncategorized / December 16, 2024 / atonu dutta / Medical device, Medical Device Consultancy, Medical Device Consultants in India, Medical device consulting in India, Medical Device Regulatory Consulting, Medtech Consultant

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

Our last blog in the series of Usability Engineering for Medical Device highlighted mandatory steps of the usability process. It

Medical Device Usability Engineering: Using Specifications Read More »

UncategorizedMedical device, Medical Device Consultancy, Medical Device Consultants in India, Medical device consulting in India, Medical Device Regulatory Consulting, Medtech Consultant

Do we need PMCF every time for every device?

Uncategorized / December 9, 2024 / sanikakulkarni / Medical device, Medical Device Consultancy, Medical device consulting companies in India, Medical device consulting in India, Medical device consulting services, Medical Device Regulatory Consultants in India, Medtech Consultant, PMCF, post market clinical follow up

PMCF, Medical Device, Medical device consulting services, Post Market Clinical Follow up,

Cath Solutions Inc. recently got a CE mark and is keen to start selling. While trying to register with the

Do we need PMCF every time for every device? Read More »

UncategorizedMedical device, Medical Device Consultancy, Medical device consulting companies in India, Medical device consulting in India, Medical device consulting services, Medical Device Regulatory Consultants in India, Medtech Consultant, PMCF, post market clinical follow up