European Medicines Agency Open data in a single API request

European Medicines Agency datasets available on official portal for European data

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Basic information

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:

  • Evaluating the safety and efficacy of medicines before they are authorized for use in the EU
  • Monitoring the safety of medicines after they have been authorized
  • Providing scientific advice to the European Commission on medicines policy
  • Cooperating with national medicines authorities in the EU
  • Promoting the development of new medicines

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:

  • Scientific evaluation
  • Risk management
  • Market authorization
  • Pharmacovigilance
  • International cooperation

What type of data they provide as open data?

The EMA provides a variety of data as open data, including:

  • Policy documents
  • Statistics
  • Data on medicines

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:

  • EU legislation on medicines
  • EMA evaluations of medicines
  • Market authorizations for medicines
  • Pharmacovigilance data
  • International cooperation activities

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:

  • CSV
  • JSON
  • XML

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.

Detailed information

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

Available datasets

Open data Portal European Medicines Agency Open Data API in development

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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

COVID-19 medicine shortages - list of national registers for medicine shortages details >

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

EMA Medicine evaluation figures (human medicines) details >

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

Medicine data: European public assessment reports (EPAR) for human medicines details >

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

ESVAC European Surveillance of Veterinary Antimicrobial Consumption database details >

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

EU Veterinary Medicinal Product Database details >

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

EudraGMDP database details >

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 Medicines Agency's list of European experts details >

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

European Union Clinical Trials Register details >

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: herbal medicines details >

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

Medicine data: paediatric investigation plans (PIP) details >

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

European Medicines Agency - documents open for public consultations details >

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

Substance, product, organisation and referential (SPOR) master data details >

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

European database of suspected adverse drug reaction reports (EudraVigilance) details >
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