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What is the European Medicines Agency (EMA)?
The European Medicines Agency (EMA) is an agency of the European Union (EU) that is responsible for the scientific evaluation of medicines. The EMA's mission is to ensure the safe and effective use of medicines in the EU.
What do they do?
The EMA's responsibilities include:
Headquarters address
The EMA's headquarters are located in Amsterdam, Netherlands.
Date of foundation
The EMA was established on 1 January 1995 by the European Commission. It was originally called the European Agency for the Evaluation of Medicinal Products (EMEA). The EMA's name was changed to the European Medicines Agency in 2004.
Who is leading the organization?
The EMA is currently led by Executive Director Emer Cooke. She was appointed Executive Director in 2019. The Executive Director is responsible for the overall management of the EMA.
Number of employees
The EMA has around 900 employees. These employees work in a variety of roles, including:
What type of data they provide as open data?
The EMA provides a variety of data as open data, including:
Write all the details about the data sets they provide as open data
The data sets that the EMA provides as open data are available on the EMA's open data portal. These data sets include information on:
What is their goal regarding open data?
The EMA's goal regarding open data is to make data on medicines more accessible and reusable for citizens, businesses, and researchers. By making data more accessible, the EMA hopes to promote transparency and accountability in the EU's medicines regulatory system.
In what formats do they provide open data?
The EMA provides open data in a variety of formats, including:
Conclusion
The European Medicines Agency (EMA) is an agency of the European Union (EU) that is responsible for the scientific evaluation of medicines. The EMA's mission is to ensure the safe and effective use of medicines in the EU. The EMA provides a variety of data as open data, including policy documents, statistics, and data on medicines. Its goal is to make data on medicines more accessible and reusable for citizens, businesses, and researchers.
Name
European Medicines Agency (EMA)
Established
1 January 1995
Headquarters
Amsterdam, Netherlands
Executive Director
Emer Cooke
Number of employees
900
Open data
Yes
Data types
Policy documents, statistics, data on medicines
Data sets
Over 100 data sets
Goal
To ensure the safe and effective use of medicines in the European Union
Formats
CSV, JSON, XML
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COVID-19 medicine shortages - list of national registers for medicine shortages Open Data
Supply disruptions or medicine shortages can occur as a result of a temporary lockdown of...
Issued on
EMA Medicine evaluation figures (human medicines) Open Data
The European Medicines Agency (EMA) publishes information on the volume and outcome of marketing...
Issued on 2016-11-09
Medicine data: European public assessment reports (EPAR) for human medicines Open Data
The EMA publishes an EPAR for every medicine granted a central marketing authorisation by the...
Issued on 2015-12-15
ESVAC European Surveillance of Veterinary Antimicrobial Consumption database Open Data
The European database of sales of veterinary antimicrobial agents provides public access to the data...
Issued on 2016-02-29
EU Veterinary Medicinal Product Database Open Data
The EU Veterinary Medicinal Product Database is intended to be a source of information on all...
Issued on 2016-11-21
EudraGMDP database Open Data
EudraGMDP is the name for the Union database referred to in article 111(6) of Directive 2001/83/EC...
Issued on 2016-11-16
European Medicines Agency's list of European experts Open Data
The European Medicines Agency (EMA) maintains a public list containing details on all European...
Issued on 2016-11-09
European Union Clinical Trials Register Open Data
The EU Clinical Trials Register contains information on interventional clinical trials on medicines...
Issued on 2016-11-16
Medicine data: herbal medicines Open Data
This search allows you to find herbal substances that are designated for assessment by the European...
Issued on 2015-12-15
Medicine data: paediatric investigation plans (PIP) Open Data
Information on opinions and decisions adopted by the European Medicines Agency's (EMA) Paediatric...
Issued on 2016-02-29
European Medicines Agency - documents open for public consultations Open Data
Access to EMA documents that are currently open for public consultation.
Issued on 2016-11-09
Substance, product, organisation and referential (SPOR) master data Open Data
The service provides access to a list of multilingual master data (terminologies, classification...
Issued on 2018-12-14T12:59:40.925959Z
European database of suspected adverse drug reaction reports (EudraVigilance) Open Data
The dataset provides data on suspected side-effects also known as suspected adverse drug reactions...
Issued on 2015-07-27
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