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Links to Free/Paid Certification Courses in Pharmacovigilance

Other Learning Resources:

MedDRA MSSO Trainings

MedDRA MSSO Trainings

2020 05 14 Data Analysis and Query Building with MedDRA

01:35:52

2020 05 14 Data Analysis and Query Building with MedDRA

Data Analysis and Query Building Language: English

2020 03 17 MedDRA Overview

01:07:47

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)

01:57:00

2020 04 28 Standardised MedDRA Queries (SMQs)

Standardised MedDRA Queries Language: English

2020 05 06 MedDRA Coding Basics

01:39:44

2020 05 06 MedDRA Coding Basics

2020 05 19 Advanced MedDRA Coding

01:45:17

2020 05 19 Advanced MedDRA Coding

Advanced MedDRA Coding Language: English

Training Resources from the European Medicines Agency (EMA)

MLM:

EMA Training Resources

1. Legal background and expected benefits

07:26

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)

42:04

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

06:51

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

18:21

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

EMA 2

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