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

With List of APIs we currently working on to bridge to life.
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Clinical trials for COVID-19 vaccination Open Data

Information on clinical trials for COVID-19 vaccines is available in the [EU Clinical Trials Registe

Issued on

Clinical trials for COVID-19 vaccination details >

COVID-19 clinical trials in the European Economic Area (EEA) Open Data

Information on ongoing COVID-19 clinical trials in the European Economic Area (EEA) is available in

Issued on

COVID-19 clinical trials in the European Economic Area (EEA) details >

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 manufactur

Issued on

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

COVID-19-related ongoing observational studies in the EU Open Data

Information on ongoing COVID-19-related observational studies in the EU is available in the European

Issued on

COVID-19-related ongoing observational studies in the EU details >

Data from the Article 57 database on all authorised medicines Open Data

The European Medicines Agency (EMA) publishes data from the Article 57 database on all medicines aut

Issued on 2018-12-13T14:22:12.416701Z

Data from the Article 57 database on all authorised medicines details >

European Medicines Agency's document library Open Data

This search allows the user to find documents published on the European Medicines Agency's website b

Issued on 2016-11-15

European Medicines Agency's document library details >

EMA Medicine evaluation figures (human medicines) Open Data

The European Medicines Agency (EMA) publishes information on the volume and outcome of marketing aut

Issued on 2016-11-09

EMA Medicine evaluation figures (human medicines) details >

EMA Medicine evaluation figures (veterinary medicines) Open Data

The European Medicines Agency (EMA) publishes information on the volume and outcome of marketing aut

Issued on 2019-01-09

EMA Medicine evaluation figures (veterinary medicines) details >

EnprEMA Network Database (EnprEMA) Open Data

This database includes research networks and centres with recognised expertise in performing clinica

Issued on 2016-11-21

EnprEMA Network Database (EnprEMA) 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 Europe

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 medici

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 a

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 exper

Issued on 2016-11-09

European Medicines Agency's list of European experts details >

European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP) Open Data

The European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP®) is a networ

Issued on 2016-11-15T10:47:38.393781Z

European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP) 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 >

European Union Clinical Trials Register - including Article 45 Paediatric Database Open Data

Database containing data on all paediatric studies completed by 26 Jan 2007 that the marketing autho

Issued on 2016-11-24

European Union Clinical Trials Register - including Article 45 Paediatric Database details >

European Medicines Agency's event and meeting calendar Open Data

Search for all EMA events, including workshops, symposia, and Committee and Management Board meeting

Issued on 2016-11-15

European Medicines Agency's event and meeting calendar 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 >

Maximum residue limit assessment reports (Veterinary medicines) Open Data

This database allows the user to access the public maximum residue limit assessment reports for acti

Issued on 2016-11-07T11:06:24.781357Z

Maximum residue limit assessment reports (Veterinary medicines) details >

Medicines for use outside the EU Open Data

This page lists the opinions given by the European Medicines Agency's Committee for Medicinal Produc

Issued on 2016-06-22T07:03:51.117177Z

Medicines for use outside the EU details >

Medicines under evaluation (Human) Open Data

This search lists information on applications for centralised marketing authorisations for human med

Issued on 2016-06-22

Medicines under evaluation (Human) details >

European Medicines Agency's news and press release archive Open Data

Search for news and press releases published on the European Medicines Agency's website by title, co

Issued on 2016-11-15

European Medicines Agency's news and press release archive details >

All European Medicines Agency (EMA) COVID-19-related web content Open Data

The European Medicines Agency (EMA) is contributing to global efforts to save lives during the COVID

Issued on

All European Medicines Agency (EMA) COVID-19-related web content details >

Medicine data: paediatric investigation plans (PIP) Open Data

Information on opinions and decisions adopted by the European Medicines Agency's (EMA) Paediatric Co

Issued on 2016-02-29

Medicine data: paediatric investigation plans (PIP) details >

Parallel Distribution (PD) register Open Data

The Parallel Distribution (PD) register provides up-to-date information on parallel distribution not

Issued on 2016-11-16

Parallel Distribution (PD) register details >

Medicine data: periodic safety update report (PSUR) single assessments Open Data

List of major changes made to the authorisation of medicines, which have been recommended by the Eur

Issued on 2016-02-29

Medicine data: periodic safety update report (PSUR) single assessments details >

Medicine data: pending EC decisions (Human medicines) Open Data

In this dataset you can find medicines that have been evaluated by the European Medicines Agency's (

Issued on 2016-02-29

Medicine data: pending EC decisions (Human medicines) details >

Pending EC decisions on maximum residue limits (Veterinary medicines) Open Data

This search allows the user to access summaries of opinion on maximum residue limits for active subs

Issued on 2016-11-07T11:11:07.559733Z

Pending EC decisions on maximum residue limits (Veterinary medicines) details >

Medicine data: pending EC decisions (Veterinary medicines) Open Data

This dataset provides a list of medicines that have been evaluated by the European Medicines Agency'

Issued on 2016-03-14

Medicine data: pending EC decisions (Veterinary medicines) details >

PROTECT project - The Pharmacoepidemiological Research on Outcomes of Therapeutics by a European... Open Data

The Pharmacoepidemiological Research on Outcomes of Therapeutics by a European Consortium is a colla

Issued on 2016-11-21

PROTECT project - The Pharmacoepidemiological Research on Outcomes of Therapeutics by a European... 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 >

European Medicines Agency's publications Open Data

Access to lists of publications (scientific articles, etc) authored by staff and experts of the Euro

Issued on 2016-11-15T09:50:32.974498Z

European Medicines Agency's publications details >

Medicine data: rare disease (orphan) designations Open Data

Information on rare disease (orphan) designations based on applications that have been assessed by t

Issued on 2016-02-29

Medicine data: rare disease (orphan) designations details >

Recommendations on medication errors Open Data

In order to promote the safe use of medicines, EMA systematically communicates on any additional mea

Issued on 2016-06-28T06:10:37.009132Z

Recommendations on medication errors details >

Medicine data: referrals for human medicines Open Data

This search allows the user to find information on referrals for human medicines assessed by the Eur

Issued on 2016-06-22

Medicine data: referrals for human medicines details >

Medicine data: referrals for veterinary medicines Open Data

The database allows the user to find information on referrals for veterinary medicines assessed by t

Issued on 2016-11-07

Medicine data: referrals for veterinary medicines details >

Medicine data: shortages Open Data

EMA assesses medicine shortages that affect or are likely to affect more than one EU Member State. F

Issued on 2016-06-28

Medicine data: shortages details >

European Medicines Agency's SME Register Open Data

Public register of Small and Medium Enterprise Companies established in the European Economic Area t

Issued on 2016-11-21T09:02:20.211746Z

European Medicines Agency's SME Register details >

Substance, product, organisation and referential (SPOR) master data Open Data

The service provides access to a list of multilingual master data (terminologies, classification sys

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 f

Issued on 2015-07-27

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

The European Union Telematics Controlled Terms (EUTCT) System Open Data

EUTCT is a repository and provider of controlled terms in multiple languages for the ongoing exchang

Issued on 2016-11-16

The European Union Telematics Controlled Terms (EUTCT) System details >

Treatments and vaccines for COVID-19: authorised medicines Open Data

Information on the medicines authorised in the European Union (EU) to treat or prevent COVID-19, fol

Issued on 2021-01-21

Treatments and vaccines for COVID-19: authorised medicines details >

Medicine data: European public assessment reports (EPAR) for veterinary medicines Open Data

The EMA publishes an EPAR for every medicine granted a central marketing authorisation by the Europe

Issued on 2015-12-15

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

Medicine data: withdrawn applications (Human medicines) Open Data

This dataset contains information on the decision by a pharmaceutical company to withdraw an applica

Issued on 2016-02-29

Medicine data: withdrawn applications (Human medicines) details >

Medicine data: withdrawn applications (Veterinary medicines) Open Data

This dataset contains information on the decision by a pharmaceutical company to withdraw an applica

Issued on 2016-03-14

Medicine data: withdrawn applications (Veterinary medicines) details >
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