MEDICAL DEVICES

Who must register and submit medical device list to FDA?

TELUGU GMP October 17, 2022

USFDA

What are the different styles of hearing aids?

TELUGU GMP August 17, 2022

USFDA

What are hearing aids and how do they work?

TELUGU GMP August 17, 2022

MEDICAL DEVICES

How are artificial intelligence and machine learning changing medical devices?

TELUGU GMP August 10, 2022

USFDA

Why does the FDA inspect and what does an FDA inspector do?

TELUGU GMP July 22, 2022

MEDICAL DEVICES

FDA 21 CFR Subchapter-H Medical Devices Regulations

TELUGU GMP December 27, 2021

MEDICAL DEVICES

FDA 21 CFR Part 800 Medical Device: General

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 801 Medical Device Labeling

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 803 Medical Device Reporting

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 806 Medical Devices: Reports Of Corrections and Removals

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 807 Establishment Registration and Device Listing

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 808 Exemptions From Federal Preemption

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 809 In Vitro Diagnostic Products For Human Use

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 810 Medical Device Recall Authority

TELUGU GMP November 26, 2021

MEDICAL DEVICES

FDA 21 CFR Part 812 Investigational Device Exemptions

TELUGU GMP November 26, 2021