Report your adverse events: Devices

preview_player
Показать описание
Part of the report your adverse events campaign, in this video we focus on encouraging consumers to report problems with medical devices. Reporting adverse events and problems with medical devices helps us better understand and improve the safety of health products in Australia.
  1. TGA Australia
  2. Therapeutic Goods Administration
  3. TGA
  4. Adverse events
  5. problems with medical devices
  6. medical devices
Рекомендации по теме
Report your adverse 0:00:16

Report your adverse events: Devices

Report your Adverse 0:00:16

Report your Adverse events: Medicines

Live Demo of 0:43:22

Live Demo of the FDA Adverse Events Reporting System (14/14) REdI 2017

Serious Adverse Event 0:04:10

Serious Adverse Event Reporting for Investigators

Reporting of Adverse 0:00:40

Reporting of Adverse Events due to medical devices - Materiovigilance Program of India

Reporting Device Adverse 0:04:42

Reporting Device Adverse Events Challenge

Electronic Submission of 0:59:21

Electronic Submission of Adverse Event Reports to FAERS using ICH E2B(R3) Standards - Oct. 11, 2019

A Bulletproof Clinical 0:58:12

A Bulletproof Clinical Evaluation Report: Making them stand up to regulatory scrutiny

Use AI to 0:00:31

Use AI to Find Use Errors in Medical Device Adverse Events and Recall Reports

ICSR Data Quality 0:34:57

ICSR Data Quality of Coding: Products, Adverse Events and Medication Errors - Pharmacovigilance 2020

How to Monitor 0:00:35

How to Monitor and Report Medical Device or IVD Adverse Events in China - China Med Device Webinar

Medical Device Adverse 0:22:05

Medical Device Adverse Events - You Don't Know What You Don't Know

Essure's Adverse Events 0:01:25

Essure's Adverse Events | Madris Tomes, CEO of Device Events

Investigator Responsibilities - 0:21:20

Investigator Responsibilities - Safety Reporting for Investigational Drugs and Devices

Safety Reporting for 0:03:47

Safety Reporting for Medical Device Studies - Responsibilities of the Investigators and Sponsor

Medical Devices: Summary 0:18:46

Medical Devices: Summary of Safety and Clinical Performance

Why electronic reporting 0:04:07

Why electronic reporting of Safety data?

Basics - Part 0:05:59

Basics - Part 10 - Adverse Event

Your Report Matters! 0:05:12

Your Report Matters! How to Report Side Effects or Product Problems with Drugs Used in Animals

How to Encourage 0:02:53

How to Encourage Adverse Event Reporting

Medical Device Adverse 0:00:45

Medical Device Adverse Event Reporting and Monitoring Regulations

US Postmarket Surveillance 0:57:13

US Postmarket Surveillance Requirements for Medical Devices

2022 NHSN Training 0:33:21

2022 NHSN Training - Device-associated SIR Analysis

Webinar Preview - 0:06:01

Webinar Preview - Monitor and Report Medical Device and IVD Adverse Events in China