+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

Results for tag: "Adverse Event Reporting"

EClinical Solutions Market Report 2025 - Product Thumbnail Image

EClinical Solutions Market Report 2025

  • Report
  • January 2025
  • 200 Pages
  • Global
From
Clinical Trial Investigative Site Network Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, 2020-2030F - Product Thumbnail Image

Clinical Trial Investigative Site Network Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, 2020-2030F

  • Report
  • February 2025
  • 185 Pages
  • Global
From
Clinical Trial Regulatory Requirements Training Course (September 15-16, 2025) - Product Thumbnail Image

Clinical Trial Regulatory Requirements Training Course (September 15-16, 2025)

  • Training
  • September 2025
  • 2 Days
  • Global
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course (September 15-16, 2025) - Product Thumbnail Image

Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course (September 15-16, 2025)

  • Training
  • September 2025
  • 2 Days
  • Global
EU (European Union) Clinical Trial Regulation 536/2014: Overview and Implementation Experience Training Course (October 13-14, 2025) - Product Thumbnail Image

EU (European Union) Clinical Trial Regulation 536/2014: Overview and Implementation Experience Training Course (October 13-14, 2025)

  • Training
  • October 2025
  • 2 Days
  • Europe
Japan Clinical Trials Support Service Market, By Region, Competition, Forecast & Opportunities, 2020-2030F - Product Thumbnail Image

Japan Clinical Trials Support Service Market, By Region, Competition, Forecast & Opportunities, 2020-2030F

  • Report
  • August 2024
  • 82 Pages
  • Japan
From
Biosimilar Suffixes Appear Superfluous In Adverse Event Reporting - Product Thumbnail Image

Biosimilar Suffixes Appear Superfluous In Adverse Event Reporting

  • Newsletter
  • August 2025
  • 4 Pages
  • Global
From
Best Practices of Drug Development & Safety, Clinical Trials & Clinical Research - Training for Quality Assurance - Product Thumbnail Image

Best Practices of Drug Development & Safety, Clinical Trials & Clinical Research - Training for Quality Assurance

  • Training
  • 13 Hours
  • Global
Clinical Trials Process: Study Sponsor's and Investigator's Responsibilities - Product Thumbnail Image

Clinical Trials Process: Study Sponsor's and Investigator's Responsibilities

  • Training
  • 60 Minutes
  • Global
U.S. Adverse Event Reporting Regulations for Drugs, Dietary Supplements and Cosmetics - Product Thumbnail Image

U.S. Adverse Event Reporting Regulations for Drugs, Dietary Supplements and Cosmetics

  • Training
  • 60 Minutes
  • United States
Practical tips to comply and implement the Adverse Event Reporting requirement of the new Dietary Supplement and Nonprescription Drug Consumer Protection Act - Product Thumbnail Image

Practical tips to comply and implement the Adverse Event Reporting requirement of the new Dietary Supplement and Nonprescription Drug Consumer Protection Act

  • Training
  • 60 Minutes
  • Global
3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada - Product Thumbnail Image

3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada

  • Training
  • 3 Hours
  • Canada, United States, ... Canada, United States, Europe
Major Changes to Clinical Trials in Europe - The New EU Clinical Trials Regulation - What Can We Expect for Compliance? - Product Thumbnail Image

Major Changes to Clinical Trials in Europe - The New EU Clinical Trials Regulation - What Can We Expect for Compliance?

  • Training
  • 60 Minutes
  • Europe
Adverse Event Reporting Requirements for Dietary Supplements and OTC Drugs - Product Thumbnail Image

Adverse Event Reporting Requirements for Dietary Supplements and OTC Drugs

  • Training
  • 90 Minutes
  • Global
Major Changes to the EU Clinical Trials Regulation: What is Required for Compliance - Product Thumbnail Image

Major Changes to the EU Clinical Trials Regulation: What is Required for Compliance

  • Training
  • 60 Minutes
  • Europe
Dietary Supplement Adverse Event Reporting and Recordkeeping Requirements under the Dietary Supplement and Nonprescription Drug Consumer Protection Act - Product Thumbnail Image

Dietary Supplement Adverse Event Reporting and Recordkeeping Requirements under the Dietary Supplement and Nonprescription Drug Consumer Protection Act

  • Training
  • 60 Minutes
  • Global
Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process Activities - Product Thumbnail Image

Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process Activities

  • Training
  • 90 Minutes
  • Global
Clinical Trials Handbook. Edition No. 1. Pharmaceutical Development Series - Product Thumbnail Image

Clinical Trials Handbook. Edition No. 1. Pharmaceutical Development Series

  • Book
  • July 2009
  • 1248 Pages
Clinical Trials Handbook. Design and Conduct. Edition No. 1 - Product Thumbnail Image

Clinical Trials Handbook. Design and Conduct. Edition No. 1

  • Book
  • December 2012
  • 600 Pages
Design, Execution, and Management of Medical Device Clinical Trials. Edition No. 1 - Product Thumbnail Image

Design, Execution, and Management of Medical Device Clinical Trials. Edition No. 1

  • Book
  • September 2009
  • 296 Pages
Loading Indicator

The Adverse Event Reporting (AER) market is a subset of the clinical trial industry, focused on the collection and analysis of data related to adverse events. AER is a critical component of clinical trials, as it helps to identify potential safety issues and ensure the safety of trial participants. AER systems are used to collect, store, and analyze data related to adverse events, and to report this data to regulatory authorities. AER systems are also used to monitor the safety of drugs and medical devices throughout the clinical trial process. AER systems are typically provided by specialized vendors, who offer a range of services, including software, data management, and consulting. These vendors typically provide a suite of products and services, including software, data management, and consulting. Some companies in the AER market include Oracle, Medidata Solutions, eClinical Solutions, and Parexel. Show Less Read more