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Results for tag: "Pharmacovigilance"

Pharmacovigilance aspects of licensing agreements - Product Thumbnail Image

Pharmacovigilance aspects of licensing agreements

  • Training
  • 60 Minutes
  • Global
Improving the Quality of Pharmaceutical Product Safety Reporting through the use of Metrics - Product Thumbnail Image

Improving the Quality of Pharmaceutical Product Safety Reporting through the use of Metrics

  • Training
  • 60 Minutes
  • Global
Introduction of Post-Marketing Drug Safety Surveillance: Pharmacovigilance in FDA / CDER - Product Thumbnail Image

Introduction of Post-Marketing Drug Safety Surveillance: Pharmacovigilance in FDA / CDER

  • Training
  • 90 Minutes
  • Global
Brazilian Regulatory System for FDA Regulated Industry: Pack of 10 Training Courses - Product Thumbnail Image

Brazilian Regulatory System for FDA Regulated Industry: Pack of 10 Training Courses

  • Training
  • 16 Hours
  • Brazil
Introduction to European Good Pharmacovigilance Practices: 4-hr Virtual Seminar - Product Thumbnail Image

Introduction to European Good Pharmacovigilance Practices: 4-hr Virtual Seminar

  • Training
  • 4 Hours
  • Europe
Scheduling and Conduct of Good Pharmacovigilance Practice Audits - Product Thumbnail Image

Scheduling and Conduct of Good Pharmacovigilance Practice Audits

  • Training
  • 90 Minutes
  • Global
How to Transition from Paper to Electronic Records in a Regulatory Environment - Product Thumbnail Image

How to Transition from Paper to Electronic Records in a Regulatory Environment

  • Training
  • 75 Minutes
  • Global
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements - Product Thumbnail Image

Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements

  • Training
  • 75 Minutes
  • Global
Clinical Trial auditing - Identifying risks and building a more compliant and successful trial - Product Thumbnail Image

Clinical Trial auditing - Identifying risks and building a more compliant and successful trial

  • Training
  • 90 Minutes
  • Global
Test Article Management and Characterization for Drugs and Devices - Product Thumbnail Image

Test Article Management and Characterization for Drugs and Devices

  • Training
  • 90 Minutes
  • Global
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial - Product Thumbnail Image

Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial

  • Training
  • 90 Minutes
  • Global
REMS Update: Risk Evaluation and Mitigation Strategies - what do you need to do now? - Product Thumbnail Image

REMS Update: Risk Evaluation and Mitigation Strategies - what do you need to do now?

  • Training
  • 60 Minutes
  • Global
The Brazilian Pharmacovigilance System - Product Thumbnail Image

The Brazilian Pharmacovigilance System

  • Training
  • 90 Minutes
  • Brazil
The New EU Clinical Trial Regulation - Product Thumbnail Image

The New EU Clinical Trial Regulation

  • Training
  • 90 Minutes
  • Europe
GAMP Data Integrity 21 CFR Part 11 Training Course - Product Thumbnail Image

GAMP Data Integrity 21 CFR Part 11 Training Course

  • Training
  • 90 Minutes
  • Global
FDA vs. EU Inspections - Getting Prepared and What are Differences - Product Thumbnail Image

FDA vs. EU Inspections - Getting Prepared and What are Differences

  • Training
  • 75 Minutes
  • 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
How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA) - Product Thumbnail Image

How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA)

  • Training
  • 60 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
Changes to Good Pharmacovigilance Practices in the EU - Product Thumbnail Image

Changes to Good Pharmacovigilance Practices in the EU

  • Training
  • 90 Minutes
  • Europe
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The Pharmacovigilance market is a subset of the Healthcare Services industry, focusing on the monitoring and assessment of the safety of pharmaceutical products. It involves the collection, analysis, and reporting of adverse events related to the use of drugs, as well as the identification of potential risks associated with their use. Pharmacovigilance activities are conducted by pharmaceutical companies, regulatory authorities, and healthcare professionals. Pharmacovigilance activities are essential for the safe and effective use of drugs, as they help to identify potential risks and ensure that the benefits of the drug outweigh the risks. Pharmacovigilance also helps to ensure that the drug is used appropriately and that any adverse events are reported and addressed. Some companies in the Pharmacovigilance market include Parexel, Quintiles, Covance, PRA Health Sciences, and ICON. Show Less Read more