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Here's a Guide to FDA Registration

Davidwaya20 Apr, 2023Other

This guide will walk you through the process of FDA registration to sell your product in the U.S. EU Declaration of Conformity Template The process can be a little confusing, which is why we made this resource to help you get your product on shelves quickly!This guide will walk you through the process of FDA registration to sell your product in the U.S. EU Declaration of Conformity Template The process can be a little confusing, which is why we made this resource to help you get your product on shelves quickly!

Sampling Plan

Davidwaya13 Feb, 2021Business

Sampling plan is a union of sample size and acceptance quality limit associated with lot acceptability criteria. A sampling plan shall describe the sample selection from a lot or multiple lots, the sample size, and the material selection (eg. Final finished product or not).

Medical Device Usability

Davidwaya07 Jan, 2021Business

I3CGLOBAL provides a Medical device usability service. It is characteristics of the User Interface that facilitate Use, to make it easier for Users to perceive information and medical devices or user interface can lead to errors. Get more information here Our expert consultants can give you further guidance. Visit now for more related information!

What Should You Know About The Medical Devices?

Davidwaya02 Dec, 2020Business

Every month, there are a lot of new medical devices which are submitted for the marketing approval from the FDA. One of them is theÂ Medical Device CE MarkingÂ which shows out the one device which will show the audience that it is purely legal and it is authorized for being a medical device.

Medical device usability

Davidwaya01 Aug, 2020Business

I3CGLOBAL provide a Medical device usability service.It is a characteristics of the User Interface that facilitate Use, to make it easier for the Users to perceive information and a medical devices or user interface can lead to errors.Get more information regarding the same to visit our website.Know more!

Medical Device Classification

Davidwaya21 Jun, 2020Business

Find out more information about Determination of the medical device classification and the corresponding classification rule is the first step in the EU CE marking process at an I3CGLOBAL. For more related information visit a website.

Class 1 medical device

Davidwaya08 Jun, 2020Business

I3CGLOBAL provide a Class I Medical Device can be self-declared for CE compliance as per the MDR. Self-declaration means neither the Notified Body certification is required nor any other.For more related information visit a website.

Biocompatibility testing

Davidwaya23 May, 2020Business

Looking for more information about Biocompatibility testing?I3CGLOBAL provide a Biocompatibility Testing Services for Medical Device is used to measure the compatibility of a product with a biological system to ensure that it is not toxic.Visit Now for more!

CE Marking for Medical Devices

Davidwaya10 May, 2020Business

I3CGLOBAL provide a Medical Device CE Marking service covering reusable medical devices, equipment, disposables, implants, drug-device combination, and home healthcare devices and more.visit a website and know more.