top of page

Links to Free/Paid Certification Courses in Pharmacovigilance

Other Learning Resources:

MedDRA MSSO Trainings

2020 05 14 Data Analysis and Query Building with MedDRA

2020 05 14 Data Analysis and Query Building with MedDRA

2020 03 17 MedDRA Overview

2020 03 17 MedDRA Overview

Date: March 17, 2020

2020 04 17 MedDRA Version 23.0 COVID-19 Update

01:01:24

2020 04 17 MedDRA Version 23.0 COVID-19 Update

Date: April 17, 2020

2020 04 28 Standardised MedDRA Queries SMQs

2020 04 28 Standardised MedDRA Queries SMQs

2020 05 06 MedDRA Coding Basics

2020 05 06 MedDRA Coding Basics

2020 05 19 Advanced MedDRA Coding

2020 05 19 Advanced MedDRA Coding

Training Resources from the European Medicines Agency (EMA)

MLM:

1. Legal background and expected benefits

1. Legal background and expected benefits

Speaker: Sabine Brosch, EMA Monitoring of medical literature and the entry of relevant information into the EudraVigilance database by the European Medicines Agency April 2015

2. Detailed guide (scope and key business processes)

2. Detailed guide (scope and key business processes)

Speaker: Sabine Brosch, EMA Monitoring of medical literature and the entry of relevant information into the EudraVigilance database by the European Medicines Agency May 2015

3. How to prepare: An outline of the necessary preparatory steps

3. How to prepare: An outline of the necessary preparatory steps

Speaker: Sabine Brosch, EMA Monitoring of medical literature and the entry of relevant information into the EudraVigilance database by the European Medicines Agency May 2015

4. New functionalities

4. New functionalities

Speaker: Thomas Paternoster-Howe, EMA Monitoring of medical literature and the entry of relevant information into the EudraVigilance database by the European Medicines Agency May 2015

Others

Module 09 - Good practice and inspections

01:18:57

Module 09 - Good practice and inspections

Moderator: Anabela Marçal, EMA - GMP supervision of manufacturers and inspections and dealing with quality defects - GCP, GLP and GVP supervision and inspections

Module 10 - Patient safety and pharmacovigilance

01:15:23

Module 10 - Patient safety and pharmacovigilance

Moderator: Peter Arlett, EMA - Overview of the EU pharmacovigilance systems - Risk management plans - Eudravigilance and signal detection - Periodic safety update reports

EV-M3a EV Reporting process for users: EV Gateway, WEB-Trader, EV-Post functions

12:05

EV-M3a EV Reporting process for users: EV Gateway, WEB-Trader, EV-Post functions

Feedback survey: https://ec.europa.eu/eusurvey/runner/EVtrainingsurvey Training Module EV-M3a EV Reporting process for users: EV Gateway, WEB-Trader, EV-Post functions Nick Halsey, Data Standardisation and Analytics, Information Management Division, EMA

Module 7: Good Practice and Inspections

01:19:40

Module 7: Good Practice and Inspections

Moderator: Anabela Marcal

bottom of page