The European Medicines Agency (EMA) produces leaflets providing information on a wide range of its activities.
Human medicines highlights 2021
English (EN) (1.16 MB - PDF)
Veterinary medicines highlights 2021
English (EN) (690.79 KB - PDF)
Human medicines highlights 2020
English (EN) (3.23 MB - PDF)
Veterinary medicines highlights 2020
English (EN) (1.37 MB - PDF)
Veterinary medicines highlights 2019
English (EN) (1.2 MB - PDF)
Human medicines highlights 2019
English (EN) (2.1 MB - PDF)
Info-card for patients: Reporting suspected side effects of medicines in patients with COVID-19
English (EN) (657.43 KB - PDF)
български (BG) (182.77 KB - PDF)
español (ES) (202.17 KB - PDF)
čeština (CS) (181.94 KB - PDF)
dansk (DA) (176.31 KB - PDF)
Deutsch (DE) (187.61 KB - PDF)
eesti keel (ET) (157.17 KB - PDF)
ελληνικά (EL) (173.67 KB - PDF)
français (FR) (177.59 KB - PDF)
hrvatski (HR) (182.21 KB - PDF)
Gaeilge (GA) (195.38 KB - PDF)
italiano (IT) (187.52 KB - PDF)
latviešu valoda (LV) (192.57 KB - PDF)
lietuvių kalba (LT) (207.92 KB - PDF)
magyar (HU) (198.48 KB - PDF)
Malti (MT) (201.97 KB - PDF)
Nederlands (NL) (166.22 KB - PDF)
polski (PL) (195.83 KB - PDF)
português (PT) (199.87 KB - PDF)
română (RO) (194.67 KB - PDF)
slovenčina (SK) (200.18 KB - PDF)
slovenščina (SL) (186.35 KB - PDF)
Suomi (FI) (162.26 KB - PDF)
svenska (SV) (198.54 KB - PDF)
Info-card for healthcare professional: Reporting suspected side effects of medicines in patients with COVID-19
English (EN) (1003.93 KB - PDF)
български (BG) (208.89 KB - PDF)
español (ES) (194.14 KB - PDF)
čeština (CS) (199.15 KB - PDF)
dansk (DA) (194.04 KB - PDF)
Deutsch (DE) (211.23 KB - PDF)
eesti keel (ET) (195.05 KB - PDF)
ελληνικά (EL) (197.19 KB - PDF)
français (FR) (209.8 KB - PDF)
hrvatski (HR) (220.62 KB - PDF)
Gaeilge (GA) (186.21 KB - PDF)
italiano (IT) (209.38 KB - PDF)
latviešu valoda (LV) (203.06 KB - PDF)
lietuvių kalba (LT) (206.79 KB - PDF)
magyar (HU) (216.54 KB - PDF)
Malti (MT) (199.95 KB - PDF)
Nederlands (NL) (212.65 KB - PDF)
polski (PL) (211.01 KB - PDF)
português (PT) (211.72 KB - PDF)
română (RO) (210.36 KB - PDF)
slovenčina (SK) (192.22 KB - PDF)
slovenščina (SL) (184.54 KB - PDF)
Suomi (FI) (197.49 KB - PDF)
svenska (SV) (195.41 KB - PDF)
World AIDS Day – Communities make the difference
English (EN) (1.06 MB - PDF)
EMA Regulatory Science to 2025 - Four goals for veterinary medicines regulation
English (EN) (1.7 MB - PDF)
Ebola vaccine development 2014-2019
English (EN) (1.06 MB - PDF)
EMA Regulatory Science to 2025 - Five goals
English (EN) (2.28 MB - PDF)
Antimicrobial resistance - Infocards
English (EN) (6.46 MB - PDF)
Responsible use of antibiotics protects animals and people - 2011-2021 Sales of antibiotics for veterinary use are down - Infographic
English (EN) (12.52 MB - PDF)
Veterinary medicines highlights 2018
English (EN) (1.4 MB - PDF)
Human medicines highlights 2018
English (EN) (1.81 MB - PDF)
Supporting medicines for children in the European Union
English (EN) (1.54 MB - PDF)
The European innovation offices network - innovators meet regulators
English (EN) (374.27 KB - PDF)
Human medicines highlights 2017
English (EN) (3.77 MB - PDF)
Veterinary medicines highlights 2017
English (EN) (2.64 MB - PDF)
1 year anniversary of clinical data publication
English (EN) (910.86 KB - PDF)
Healthy animals, healthy people - leaflet
English (EN) (161.56 KB - PDF)
Enabling science that works for patients – leaflet
English (EN) (953.22 KB - PDF)
Patients, consumers, healthcare professionals key figures - 2017
English (EN) (922.32 KB - PDF)
PRIME - The first 12 months
English (EN) (993.8 KB - PDF)
Biosimilars in the EU - Information guide for healthcare professionals
English (EN) (1.96 MB - PDF)
български (BG) (1.9 MB - PDF)
español (ES) (1.94 MB - PDF)
čeština (CS) (1.89 MB - PDF)
dansk (DA) (1.87 MB - PDF)
Deutsch (DE) (1.9 MB - PDF)
eesti keel (ET) (755.5 KB - PDF)
ελληνικά (EL) (1.94 MB - PDF)
français (FR) (1.89 MB - PDF)
hrvatski (HR) (1.95 MB - PDF)
italiano (IT) (1.95 MB - PDF)
latviešu valoda (LV) (1.9 MB - PDF)
lietuvių kalba (LT) (1.94 MB - PDF)
magyar (HU) (1.96 MB - PDF)
Malti (MT) (825.65 KB - PDF)
Nederlands (NL) (1.97 MB - PDF)
polski (PL) (2 MB - PDF)
português (PT) (1.95 MB - PDF)
română (RO) (1.96 MB - PDF)
slovenčina (SK) (1.96 MB - PDF)
slovenščina (SL) (1.96 MB - PDF)
Suomi (FI) (1.79 MB - PDF)
svenska (SV) (1.93 MB - PDF)
Veterinary medicines highlights 2016
English (EN) (383.75 KB - PDF)
Human medicines highlights 2016
English (EN) (1.42 MB - PDF)
Conditional Marketing Authorisation - How early access to medicines has helped patients from 2006 to 2016
English (EN) (1.76 MB - PDF)
The work of the European Medicines Agency - Vital for EU public and animal health and the pharmaceutical industry
English (EN) (302.34 KB - PDF)
The EU clinical trial portal and database
English (EN) (230.34 KB - PDF)
Early access to medicines - Development support and regulatory tools
English (EN) (300.45 KB - PDF)
PRIME – Paving the way for promising medicines for patients - Factsheet
English (EN) (773.58 KB - PDF)
Veterinary medicines highlights 2015
English (EN) (642.85 KB - PDF)
Human medicines highlights 2015
English (EN) (807.54 KB - PDF)
European Medicines Agency 1995-2015 - Working together for safe and effective medicines
English (EN) (195.56 KB - PDF)
Supporting regulatory science outside the EU - The Article 58 procedure
English (EN) (418.09 KB - PDF)
International Cooperation - European Medicines Agency
English (EN) (227.79 KB - PDF)
Did you know? You can report side effects yourself
As a patient, you have the right to report unwanted side effects of medicines directly to the authorities. You can also report a side effect on behalf of someone in your care, such as a child or relative.
English (EN) (181.61 KB - PDF)
български (BG) (186.38 KB - PDF)
español (ES) (188.92 KB - PDF)
čeština (CS) (247.51 KB - PDF)
dansk (DA) (178.63 KB - PDF)
Deutsch (DE) (188.93 KB - PDF)
eesti keel (ET) (175.83 KB - PDF)
ελληνικά (EL) (190.34 KB - PDF)
français (FR) (187.09 KB - PDF)
hrvatski (HR) (200.71 KB - PDF)
íslenska (IS) (191.56 KB - PDF)
italiano (IT) (184.26 KB - PDF)
latviešu valoda (LV) (192.56 KB - PDF)
lietuvių kalba (LT) (194.42 KB - PDF)
magyar (HU) (194.66 KB - PDF)
Malti (MT) (196.75 KB - PDF)
Nederlands (NL) (187.7 KB - PDF)
norsk (NO) (177.88 KB - PDF)
polski (PL) (199.44 KB - PDF)
português (PT) (184.25 KB - PDF)
română (RO) (187.82 KB - PDF)
slovenčina (SK) (184.89 KB - PDF)
slovenščina (SL) (187.7 KB - PDF)
Suomi (FI) (179.82 KB - PDF)
svenska (SV) (188.68 KB - PDF)
The European regulatory system for medicines
English (EN) (1.37 MB - PDF)
български (BG) (1.17 MB - PDF)
español (ES) (1.12 MB - PDF)
čeština (CS) (1.16 MB - PDF)
dansk (DA) (1.12 MB - PDF)
Deutsch (DE) (1.12 MB - PDF)
eesti keel (ET) (1.08 MB - PDF)
ελληνικά (EL) (1.15 MB - PDF)
français (FR) (1.11 MB - PDF)
hrvatski (HR) (1.14 MB - PDF)
íslenska (IS) (1.13 MB - PDF)
Gaeilge (GA) (1.12 MB - PDF)
italiano (IT) (1.14 MB - PDF)
latviešu valoda (LV) (1.15 MB - PDF)
lietuvių kalba (LT) (1.16 MB - PDF)
magyar (HU) (1.15 MB - PDF)
Malti (MT) (1.19 MB - PDF)
Nederlands (NL) (1.13 MB - PDF)
norsk (NO) (1.11 MB - PDF)
polski (PL) (1.17 MB - PDF)
português (PT) (1.13 MB - PDF)
română (RO) (1.16 MB - PDF)
slovenčina (SK) (1.17 MB - PDF)
slovenščina (SL) (1.17 MB - PDF)
Suomi (FI) (1.09 MB - PDF)
svenska (SV) (1.11 MB - PDF)
Overview of the European Medicines Agency’s role, activities and priorities for 2015
English (EN) (305.41 KB - PDF)
Applying for European Union marketing authorisation for medicinal products for human use
English (EN) (289.34 KB - PDF)
Applying for EU marketing authorisation for medicinal products for veterinary use
English (EN) (353.61 KB - PDF)
Advanced-therapy medicinal products and the CAT
English (EN) (521.04 KB - PDF)
Biological medicinal products
English (EN) (569.11 KB - PDF)
Biosimilar medicinal products
English (EN) (286.09 KB - PDF)
Business pipeline
English (EN) (351.78 KB - PDF)
EU Clinical Trials Register
English (EN) (446.7 KB - PDF)
The European Network of Centres for Pharmacoepidemiology and Pharmacovigilance
English (EN) (1006.09 KB - PDF)
Enpr-EMA European Network of Paediatric Research at the European Medicines Agency
The European Network of Paediatric
Research at the European Medicines
Agency (Enpr-EMA) is a network of
research networks, investigators and
centres with recognised expertise in
performing clinical trials in the
paediatric
population.
English (EN) (318.58 KB - PDF)
Environmental risk-assessment of medicines
English (EN) (426.45 KB - PDF)
European Union enlargement programme
English (EN) (259.08 KB - PDF)
Orphan-medicinal-product designation
English (EN) (293.06 KB - PDF)
Pharmacovigilance
English (EN) (298.08 KB - PDF)
Pharmacovigilance: Information systems and services
English (EN) (301.53 KB - PDF)
Better vigilance for health protection and innovation
English (EN) (310.45 KB - PDF)
Scientific advice and protocol assistance
English (EN) (691.67 KB - PDF)
Better medicines for children
English (EN) (247.68 KB - PDF)
Improving medicines for older people
English (EN) (253.7 KB - PDF)
Career opportunities at the European Medicines Agency
English (EN) (196.92 KB - PDF)
Trainee programme at the European Medicines Agency
English (EN) (185.04 KB - PDF)