Sara Williams

4 yrs - Translate

Medical Device Labelling Requirements
#medicaldevice #iso15223 #fda

Medical device Labelling Requirements - ISO 15223-1:2016

www.reghelps.com

Medical device Labelling Requirements - ISO 15223-1:2016

Medical device labelling is known in the context of the Food Drug and Cosmetic Act (FDCA) and goes beyond the printed label that is placed on the device. It’ll include all accompanying brochure documents, manuals, marketing material, and websites.

Like

Comment

Share

4 yrs - Translate

Best Medical Device Registration Services in the Europe
#fda #fdaregistration #medicaldevice

Medical Device Registration & Device Listing - Best FDA Specialist

www.reghelps.com

Medical Device Registration & Device Listing - Best FDA Specialist

Get FDA Medical device registration & device listing services at lowest fee, and will be completed in just 2-3 days. Contact us for hassle free services.

Like

Comment

Share

4 yrs - Translate

FDA 21 CFR 820 IMPLEMENTATION
#fda #fdaconsultation #fdainspection

21 CFR Part 820 Implementation – Top FDA Consultation

www.reghelps.com

21 CFR Part 820 Implementation – Top FDA Consultation

FDA inspects (QSIT)) medical device producers registered facilities on a regular basis to ensure that internal quality procedures and systems are in compliance with or in violation of 21 CFR part 820 standards.

Like

Comment

Share

4 yrs - Translate

FDA Medical Device Classification
#medicaldeviceclassification #fda #usfda

FDA Medical Device Classification & Regulatory Controls

www.reghelps.com

FDA Medical Device Classification & Regulatory Controls

The FDA classifies medical devices depending on the risk they pose to the user. The FDA divides devices into three classes: Class I (low risk), Class II (moderate risk), and Class III (high risk) (high risk).

Like

Comment

Share

4 yrs - Translate

FDA 510(k) Premarket Notification
#510k #fda #medicaldevice #usfda

Medical Device FDA 510k Premarket Notification - Know Everything

www.reghelps.com

Medical Device FDA 510k Premarket Notification - Know Everything

A 510k notification is a premarket submission made to FDA that demonstrates the device to be sold is as safe and effective, that is, substantially equivalent, to a legally marketed device.

Like

Comment

Share

Load more posts

Info

13 posts
https://www.reghelps.com/
Female
11/30/-1
Working at Reghelps
Living in Germany
Social Links

About

One of the best Regulatory Consultant in Europe.

Albums

0

Friends

1

Danny Huff

Likes

0

Groups

0