Progress: Procedure completed
Role | Committee | Rapporteur | Shadows |
---|---|---|---|
Lead | CONT | CZARNECKI Ryszard ( ECR) | NOVAKOV Andrey ( EPP), WOLTERS Lara ( S&D), CSEH Katalin ( Renew), EICKHOUT Bas ( Verts/ALE), KUHS Joachim ( ID), OMARJEE Younous ( GUE/NGL) |
Committee Opinion | ENVI | CANFIN Pascal ( Renew) | Stanislav POLČÁK ( PPE) |
Lead committee dossier:
Subjects
Events
The European Parliament decided to grant discharge to the Executive Director of the European Food Safety Authority (EFSA) for the financial year 2018 and to approve the closure of the accounts for the financial year in question.
Noting that the Court of Auditors has stated that it has obtained reasonable assurances that the Authority’s annual accounts for the financial year 2018 are reliable and that the underlying transactions are legal and regular, Parliament adopted by 604 votes to 53 with 36 abstentions, a resolution containing a series of recommendations, which form an integral part of the decision on discharge and which add to the general recommendations set out in the resolution on performance, financial management and control of EU agencies:
Authority’s financial statements
The final budget of the European Food Safety Authority for the financial year 2018 was EUR 79 183 814.25, representing a slight decrease of 0.47 % compared to 2017.
Budget and financial management
The budget monitoring efforts during the financial year 2018 resulted in a budget implementation rate of 100 %, representing a slight increase of 0.02 % compared to 2017. The payment appropriations execution rate was at 91.31 %, representing a decrease of 1 % compared to 2017.
Other observations
Members also made a series of observations regarding performance, staff policy, procurement and internal controls.
In particular, they noted that:
- 2018 was the second year of the comprehensive performance-based management approach, of the measurement of the Authority’s performance based on new key performance indicators and of the implementation of the Authority’s Strategy 2020 plan;
- the Authority finalised 788 questions through scientific opinions, technical reports and supporting publications;
- on 31 December 2018, the establishment plan was 97.49 % executed, with 5 officials and 306 temporary agents appointed out of 319 posts authorised under the Union budget;
- the Authority was hit by conflicts of interest problems and a fitness-check was carried out with the aim of assessing how to revise the Authority’s Anti-Fraud Strategy in 2019;
- the Authority shall make efforts in providing Union risk managers with comprehensive, independent and up-to-date scientific advice on questions linked to the food chain, communicating clearly to the public on its outputs and the information on which they are based, and cooperating with interested parties and institutional partners to promote coherence and trust in the Union food safety system.
Documents
- Results of vote in Parliament: Results of vote in Parliament
- Decision by Parliament: T9-0113/2020
- Committee report tabled for plenary, single reading: A9-0068/2020
- Committee report tabled for plenary: A9-0068/2020
- Supplementary non-legislative basic document: 05761/2020
- Amendments tabled in committee: PE646.781
- Committee opinion: PE641.158
- Committee draft report: PE639.854
- Non-legislative basic document: COM(2019)0316
- Non-legislative basic document: EUR-Lex
- Non-legislative basic document published: COM(2019)0316
- Non-legislative basic document published: EUR-Lex
- Non-legislative basic document: COM(2019)0316 EUR-Lex
- Committee draft report: PE639.854
- Committee opinion: PE641.158
- Amendments tabled in committee: PE646.781
- Supplementary non-legislative basic document: 05761/2020
- Committee report tabled for plenary, single reading: A9-0068/2020
Votes
A9-0068/2020 - Ryszard Czarnecki - Décision #
A9-0068/2020 - Ryszard Czarnecki - Résolution #
Amendments | Dossier |
11 |
2019/2078(DEC)
2019/12/11
ENVI
11 amendments...
Amendment 1 #
Draft opinion Paragraph 4 a (new) 4 a. Notes with concern that the Authority, as one of the Union regulatory agencies responsible for risk assessment of regulated products, does not receive sufficient resources to carry out effectively its responsibilities; insists that the Authority is granted sufficient resources to carry out its tasks;
Amendment 10 #
Draft opinion Paragraph 8 8. Notes that following the results of the third external evaluation of the Authority, the Management Board adopted a series of recommendations, focusing on enhancing the Authority’s capacity for fit- for-purpose scientific advice, bolstering communication activities to strengthen the Authority’s reputation and securing the long-term efficiency and sustainability of the Authority’s operations; stresses the need to ensure the Authority's independence, given that some of its officials have been accused of having conflicts of interest and connections with the companies whose products it was supposed to be monitoring, and, in some cases, passing on arguments from their internal scientific reports;
Amendment 11 #
Draft opinion Paragraph 9 9. Notes with satisfaction that the Authority cooperates with other agencies working on complementary tasks, i.e. the European Centre for Disease Prevention and Control (ECDC), the European Chemicals Agency and the European Medicines Agency, e.g. in the areas of data collection and analysis and databases (e.g. zoonoses, antimicrobial resistance, molecular typing), in scientific assessments (e.g. rapid outbreak assessments with the ECDC), or risk assessment; stresses the importance of cooperation at EU and international level, including with Member States, EU bodies and institutions, scientific organisations, international organisations, and third countries;
Amendment 2 #
Draft opinion Paragraph 6 6. Believes that the Authority should continue paying special attention to public opinion, and commit itself to openness and transparency;
Amendment 3 #
Draft opinion Paragraph 6 6. Believes that the Authority should continue paying special attention to public opinion, and commit itself to increased openness and increased transparency;
Amendment 4 #
Draft opinion Paragraph 6 6. Believes that the Authority should continue paying special attention to public
Amendment 5 #
Draft opinion Paragraph 7 7. Welcomes that, following adoption of its new policy on independence in 2017,
Amendment 6 #
Draft opinion Paragraph 7 a (new) 7 a. Regrets that, in relation to the two- year cooling-off period, the 2017 independence policy includes the obligation to screen experts' interests only in relation to the mandate of the scientific group to which the expert is applying; calls for the policy to be updated without delay in order to ensure that experts' interests are viewed within the context of the overall remit of the Authority, as repeatedly called for by Parliament;
Amendment 7 #
Draft opinion Paragraph 7 b (new) 7 b. Regrets that the research funding from companies in the Authority's remit is not considered relevant to the cooling-off period as long as amounts at stake do not rise above 25 % of the total research budget managed by the expert and/or their research team, and that the threshold is applied to individual sources as opposed to all private sources combined; calls for the funding threshold to be removed from the Authority's independence policy, in line with Parliament's repeated requests on the matter;
Amendment 8 #
Draft opinion Paragraph 7 c (new) 7 c. Recalls that the Authority already has the possibility to organise expert hearings to which they can invite any expert, regardless of any conflict of interest, to answer questions posed by a scientific panel without the expert having the right to participate in the panel's deliberations and drafting of the opinion;
Amendment 9 #
Draft opinion Paragraph 7 d (new) 7 d. Recalls that the revised Regulation (EC) No 178/20021a will require the Authority to pro-actively make regulatory data, that has been submitted by applicants, available to be downloaded, printed and searched through in an electronic format; whereas this will allow the Authority to benefit from extended peer review of the scientific community; recalls that this transparency requirement is indispensable for industry-sponsored research but it cannot be used as an argument to refuse academic data using data kept confidential for legitimate reasons, such as patients' personal medical records; _________________ 1aRegulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (OJ L 031 1.2.2002, p. 1).
source: 641.159
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