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Text · Opinion parliamentary committee draft

On discharge in respect of the implementation of the general budget of the European Medicines Agency for the financial year 2022

Document ENVI-PA-754678 · 2023/2156(DEC)

Kind
Opinion parliamentary committee draft ENVI-PA-754678
Date
7 November 2023
Committee
Committee on the Environment, Public Health and Food Safety
Rapporteur
Pascal Canfin
Dossier
2023-2156
More facts (3)
Subject matter
BUDG
Reference
2023/2156(DEC)
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In short

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AI: In short Written by AI from the official text — check the source · deepseek-flash · 25 Sept 2026

This is a draft opinion by Parliament's Committee on the Environment, Public Health and Food Safety on granting discharge to the European Medicines Agency for its 2022 budget. It recommends discharge and sets out findings on the agency's budget, revenue, staffing, medicines authorisations, cybersecurity, animal testing and veterinary rules.

Position. The committee recommends, based on the facts available, that discharge be granted to the Executive Director of the European Medicines Agency for the implementation of its 2022 budget, and asks the Committee on Budgets to include its suggestions in the discharge resolution.

Key points

  1. The committee calls on the Committee on Budgets to include its suggestions in the discharge resolution.
  2. It restates the European Medicines Agency's role in protecting human and animal public health by assessing and supervising medicines.
  3. It notes the agency's total final appropriations for 2022 of EUR 421 815 000, an 11,22% increase on 2021.
  4. It recalls that the agency is fee-funded: 88,27% of 2022 revenue came from pharmaceutical industry fees, 11,70% from the Union budget and 0,02% from other sources.
  5. It notes that 658 of 662 authorised posts were occupied on 31 December 2022, against 644 of 657 in 2021.
  6. It acknowledges that 2022 still involved significant COVID-19 related activities, shifting from pre- and initial marketing authorisation to post-authorisation activities.
  7. It notes that the agency recommended marketing authorisation in 2022 for 89 new human medicines, including 41 new active substances, and 10 new veterinary medicines, including 3 new active substances and 2 vaccines.
  8. It welcomes measures taken after the December 2020 cyberattack, including the 2021-2022 Information Security Management Steering Committee overseeing the agency's information security strategy.
  9. It stresses that replacing animal testing should be a priority under the 3Rs principles, and notes the November 2022 launch of a joint 3Rs working party of the human and veterinary medicines committees.
  10. It welcomes the agency's implementation of Regulation 2019/6 on veterinary medicinal products and Regulation 536/2014 on clinical trials.
  11. It recommends that discharge be granted to the agency's Executive Director for the implementation of the 2022 budget.

Who is affected

  • The European Medicines Agency: the opinion recommends granting discharge for its 2022 budget and reviews its finances and activities.
  • The pharmaceutical industry: it pays fees that made up 88,27% of the agency's 2022 revenue.
  • The Committee on Budgets: it is asked to incorporate the suggestions into its discharge resolution.

Figures and deadlines

  • EUR 421 815 000 — the agency's total final appropriations for 2022.
  • 11,22% — the increase in the 2022 budget compared to 2021.
  • 88,27% — share of 2022 revenue from pharmaceutical industry fees.
  • 11,70% — share of 2022 revenue from the Union budget.
  • 0,02% — share of 2022 revenue from various other sources.
  • 658 of 662 — authorised posts occupied on 31 December 2022.
  • 644 posts out of 657 — occupied in 2021.
  • 89 new human medicines, including 41 new active substances, and 10 new veterinary medicines, including 3 new active substances and 2 vaccines — recommended for marketing authorisation in 2022.

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Suggestions

The Committee on the Environment, Public Health and Food Safety calls on the Committee on Budgets, as the committee responsible, to incorporate the following suggestions into its motion for a resolution:

1. Reiterates the key role of the European Medicines Agency ('the EMA') in protecting and promoting human and animal public health by assessing and supervising medicines for human or veterinary use;

2. Notes that the EMA's total final appropriations for 2022 amounted to EUR 421 815 000, representing a 11,22% increase compared to the 2021 budget,

3. Recalls that the EMA is a fee-funded agency, with 88,27 % of its 2022 revenue stemming from fees paid by the pharmaceutical industry for services provided, 11,70 % stemming from the Union budget and 0,02 % from various other sources;

4. Notes that 658 of the 662 authorised posts were occupied on 31 December 2022, compared to the 644 posts out of 657 in 2021;

5. Acknowledges that 2022 was still characterised by a significant level of COVID-19 related activities, with a shift from pre and initial marketing authorisation activities to post-authorisation activities

6 Notes that EMA recommended in 2022 marketing authorisation for 89 new human medicines, including 41 new active substances, and 10 new veterinary medicines, including 3 new active substances and 2 vaccines.

7 Welcomes the fact that, following the cyberattack in December 2020, EMA has taken various measures to further enhance its cybersecurity capabilities, including the establishment in 2021-2022 of the Information Security Management Steering Committee, a senior-level governance board with the primary responsibility to oversee the implementation of the Agency’s Information Security Strategy;

8 Stresses that the replacement of animal testing shall be a priority in medicine development during the application of the 3Rs - replace, reduce and refine animal use for the development, manufacturing and testing of medicines– principles; notes that in November 2022, EMA activated a new Joint 3Rs Working Party of the Committee for Medicinal Products for Human Use (CHMP) and the Committee for Veterinary Medicinal Products (CVMP).

9 Welcomes EMA’s implementation of the EU Regulation 2019/6 on Veterinary Medicinal Products Regulation, aiming to boost innovation and increase availability of safe and high-quality veterinary medicines for treating and preventing animal diseases, as well as the implementation of the EU Regulation 536/2014 on Clinical Trials.

10. Recommends, based on the facts available, that discharge be granted to the Executive Director of the European Medicines Agency in respect of the implementation of the EMA's budget for the financial year 2022.

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Sources & citation

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Data source
Licensed CC BY 4.0.
Retrieved
25 September 2026

Cite as

European Parliament (2023). “DRAFT OPINION on discharge in respect of the implementation of the general budget of the European Medicines Agency for the financial year 2022”. Text, 7 November 2023. docId ENVI-PA-754678. EU Parl Watch Research. https://news.eu-parl.st-solutions.dev/texts/ENVI-PA-754678 (retrieved 25 September 2026). Data: EP Open Data API: document record, https://data.europarl.europa.eu/api/v2/documents/ENVI-PA-754678 (CC BY 4.0).
BibTeX
@misc{epw-text-envi-pa-754678,
  author = {{European Parliament}},
  title = {{DRAFT OPINION on discharge in respect of the implementation of the general budget of the European Medicines Agency for the financial year 2022}},
  year = {2023},
  date = {2023-11-07},
  howpublished = {\url{https://news.eu-parl.st-solutions.dev/texts/ENVI-PA-754678}},
  url = {https://news.eu-parl.st-solutions.dev/texts/ENVI-PA-754678},
  urldate = {2026-09-25},
  publisher = {EU Parl Watch Research},
  note = {Text. docId ENVI-PA-754678. Data: EP Open Data API: document record (CC BY 4.0)}
}