Progress: Procedure completed
Role | Committee | Rapporteur | Shadows |
---|---|---|---|
Lead | CONT | VAUGHAN Derek ( S&D) | DEUTSCH Tamás ( PPE), VISTISEN Anders ( ECR), ALI Nedzhmi ( ALDE), JÁVOR Benedek ( Verts/ALE), VALLI Marco ( EFDD), KAPPEL Barbara ( ENF) |
Committee Opinion | ENVI | LA VIA Giovanni ( PPE) | Julie GIRLING ( ECR), Benedek JÁVOR ( Verts/ALE), Karin KADENBACH ( S&D), Jasenko SELIMOVIC ( ALDE) |
Lead committee dossier:
Subjects
Events
PURPOSE: to grant discharge to the European Medicines Agency (EMA) for the financial year 2014.
NON-LEGISLATIVE ACT: Decision (EU) 2016/1534 of the European Parliament on discharge in respect of the implementation of the budget of the European Medicines Agency for the financial year 2014.
CONTENT: with this Decision, the European Parliament gives discharge to the Executive Director of the European Medicines Agency for the implementation of the Agency’s budget for 2014.
The Decision is consistent with the European Parliament’s resolution adopted on 28 April 2016 and includes a series of observations that form an integral part of the discharge decision (refer to the summary of the opinion of 28 April 2016).
Amongst Parliament’s main observations in the resolution accompanying the discharge decision, it broached the difficulties on the legality and regularity of transactions . It noted that the Agency’s Fee Regulation provides due dates for the collection of fees from applicants and the Agency’s related payments to national competent authorities. These due dates were not respected for most of the transactions audited by the Court. It called on the Agency to take all measures necessary to remedy this issue.
The European Parliament decided to grant discharge to the Executive Director of the European Medicines Agency (EMA) in respect of the implementation of its budget for the financial year 2014. The vote on the decision on discharge covers the closure of the accounts (in accordance with Annex V, Article 5 (1)(a) to Parliament’s Rules of Procedure.
Noting that the Court of Auditors has stated that it has obtained reasonable assurances that the Agency’s annual accounts for the financial year 2014 are reliable and that the underlying transactions are legal and regular, Parliament adopted by 516 votes to 113 with 10 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:
Agency’s financial statements : Parliament noted the final budget of the European Medicines Agency for the financial year 2014 was EUR 282 474 000, representing an increase of 12.29 % compared to 2013. 12.53 % of the Agency's budget derives from the Union budget. Legality and regularity of transactions : Parliament noted that the Agency’s Fee Regulation provides due dates for the collection of fees from applicants and the Agency’s related payments to national competent authorities. It noted that these due dates were not respected for most of the transactions audited by the Court. It called on the Agency to report to the discharge authority on measures implemented to remedy this issue. Parliament also made a series of observations regarding commitments and carryovers, procedures for contract awards, recruitment, internal control and audit. Conflicts of interest : Parliament acknowledged that the Agency has defined what are direct and indirect interests and ordered all experts to declare all direct and indirect interests in their annual declaration of interests. Moreover, it noted that restrictions are applied to experts declaring direct or indirect interests which depend on the activity in which they are involved, maintaining the policy distinction between those interests in line with the relevant legislation.
Lastly, Parliament recalled that the Pharmacovigilance Fee Regulation was published in the Official Journal of the European Union on 27 June 2014 and has applied to procedures starting from 26 August 2014, although annual fees to support information technology systems and literature monitoring activities will not be levied until 2015. It stressed that that Regulation now allows the Agency to collect fees from marketing authorisation holders to finance these pharmacovigilance activities conducted at Union level in respect of medicinal products for human use. It pointed out that the income is used to remunerate national competent authorities for the scientific assessment carried out by the rapporteurs of the Agency’s Pharmacovigilance Risk Assessment Committee and contributes to the pharmacovigilance costs of the Agency.
The Committee on Budgetary Control adopted the report by Derek VAUGHAN (S&D, UK) on discharge in respect of the implementation of the budget of the European Medicines Agency for the financial year 2014.
The parliamentary committee calls on the European Parliament to grant the Executive Director of the Agency discharge in respect of the implementation of the agency’s budget for the financial year 2014.
Noting that the Court of Auditors issued a statement of assurance as to the reliability of the accounts and the legality and regularity of the underlying transactions for the financial year 2014, Members call on Parliament to approve the closure of the Agency’s accounts. They made, however, a number of recommendations that needed to be taken into account when the discharge is granted, in addition to the general recommendations that appear in the draft resolution on performance, financial management and control of EU agencies :
· Agency’s financial statements: Members note the final budget of the European Medicines Agency for the financial year 2014 was EUR 282 474 000, representing an increase of 12.29 % compared to 2013. 12.53 % of the Agency's budget derives from the Union budget.
· Legality and regularity of transactions: Members note that the Agency’s Fee Regulation provides due dates for the collection of fees from applicants and the Agency’s related payments to national competent authorities. They note that these due dates were not respected for most of the transactions audited by the Court. They call on the Agency to report to the discharge authority on measures implemented to remedy this issue
Members also made a series of observations regarding commitments and carryovers, procedures for contract awards, recruitment, internal control and audit.
Members note the Agency revised its policy on handling of declarations of interests of scientific committee members and experts. It defined what are direct and indirect interests and ordered all experts to declare all direct and indirect interests in their annual declaration of interests. They note, moreover, that restrictions are applied to experts declaring direct or indirect interests which depend on the activity in which they are involved , maintaining the policy distinction between those interests in line with the relevant legislation.
Lastly, Members recall that the Pharmacovigilance Fee Regulation was published in the Official Journal of the European Union on 27 June 2014 and has applied to procedures starting from 26 August 2014, although annual fees to support information technology systems and literature monitoring activities will not be levied until 2015. They stress that that Regulation now allows the Agency to collect fees from marketing authorisation holders to finance these pharmacovigilance activities conducted at Union level in respect of medicinal products for human use. They point out that the income is used to remunerate national competent authorities for the scientific assessment carried out by the rapporteurs of the Agency’s Pharmacovigilance Risk Assessment Committee and contributes to the pharmacovigilance costs of the Agency.
Having examined the revenue and expenditure accounts for the financial year 2014 and the balance sheet as at 31 December 2014 of the European Medicines Agency (EMA), as well as the Court of Auditors' report on the annual accounts of the Agency for the financial year 2014, accompanied by the Agency's replies to the Court's observations, the Council recommended the European Parliament to give a discharge to the Executive Director of the Agency in respect of the implementation of the budget for the financial year 2014.
The Council welcomed the Court's opinion that, in all material respects, the Agency's annual accounts present fairly its financial position as at 31 December 2014 and the results of its operations and its cash flows for the year then ended, in accordance with the provisions of the Agency's Financial Regulation, and that the underlying transactions for 2014 are legal and regular in all material respects.
Nevertheless, the Council has made some observations which may be summarised as follows:
fees : the Council noted the Court's observation that the Agency did not ensure that the due dates for the collection of fees and the related payments to the National Competent Authorities were respected. It encouraged the Agency to pursue its efforts to comply with the Agency's own fee regulation; management control : the Council welcomed the Agency's corrective measures, but regretted the deficiencies found by the Court in the Agency's management control. It urged the Agency to thoroughly evaluate the effectiveness of the measures taken; procurement procedures : lastly, the Council encouraged the Agency to further improve its procurement procedures in order to ensure their effectiveness.
PURPOSE: presentation of the EU Court of Auditors’ report on the annual accounts of the European Medicines Agency for the financial year 2014, together with the Agency’s reply.
CONTENT: in accordance with the tasks conferred on the Court of Auditors by the Treaty on the Functioning of the European Union, the Court presents to the European Parliament and to the Council, in the context of the discharge procedure, a Statement of Assurance as to the reliability of the annual accounts of each institution, body or agency of the EU, and the legality and regularity of the transactions underlying them, on the basis of an independent external audit.
This audit concerned, amongst others, the annual accounts of the European Medicines Agency (EMA).
Statement of assurance : pursuant to the provisions of Article 287 of the Treaty on the Functioning of the European Union (TFEU), the Court has audited:
the annual accounts of the Agency, which comprise the financial statements and the reports on the implementation of the budget for the financial year ended 31 December 2014, and the legality and regularity of the transactions underlying those accounts.
Opinion on the reliability of the accounts : in the Court’s opinion, the Agency’s annual accounts present fairly, in all material respects, its financial position as at 31 December 2014 and the results of its operations and its cash flows for the year then ended, in accordance with the provisions of its Financial Regulation and the accounting rules adopted by the Commission’s accounting officer.
Opinion on the legality and regularity of the transactions underlying the accounts : in the Court’s opinion, the transactions underlying the annual accounts for the year ended 31 December 2014 are legal and regular in all material respects.
The report also makes a series of observations on the budgetary and financial management of the Agency, accompanied by the latter’s response. The main observations may be summarised as follows:
The Court’s observations :
legality and regularity of transactions : the Court noted that due dates for the collections fees from applicants and the Agency’s related payments to National Competent Authorities were not respected; public procurement : the Court noted that in 2014, the Agency concluded a EUR 15 million framework contract (covering the years 2014 to 2017) for high-level management consultancy services. The objectives and activities to be carried out were not sufficiently specific to justify the procurement decision or the volume of the contract.
The Agency’s response :
legality and regularity of transactions : the Agency stated that during 2013-14, the Agency has redesigned and streamlined its main operational processes including financial authorisations and fee collections. The further planned automation of the latter was delayed because of the Agency’s reorganisation in 2014. To ensure compliance with the Agency’s fee regulation concerning due dates, this automation is now planned to be implemented by the end of 2015; public procurement : the Agency rejected the Court’s position and stated that it had clearly assessed the needs to justify a call for tender.
Lastly, the Court of Auditors’ report contains a summary of the Agency’s activities in 2014 . This is focused on the following:
Budget : EUR 282.47 of which the Union contribution amounts to 8.2 %.
Activities :
applications for marketing authorisations for 100 medicines for human use; applications for marketing authorisations for 12 medicinal products for veterinary use; 506 inspections; herbal medicinal product studies; 329 applications for orphan medicinal products; requests for SME status: 499 requests and 333 applications for fee reduction or deferrals.
PURPOSE: presentation by the Commission of the consolidated annual accounts of the European Union for the financial year 2014, as part of the 2014 discharge procedure.
Analysis of the accounts of the European Medicines Agency (EMEA) .
CONTENT: this Commission document sets out the consolidated annual accounts of the European Union for the financial year 2014 as prepared on the basis of the information presented by the institutions, organisations and bodies of the EU, in accordance with Article 148 (2) of the Financial Regulation applicable to the EU's General Budget, including the European Medicines Agency (EMEA).
The document contains the figures on which the discharge procedure is based.
On this basis, the Financial Controller of the European Commission ensures the certification of the consolidated accounts as declared by the institutions, agencies and bodies of the European Union.
Discharge procedure of the EU agencies : the EU Budget finances a wide range of policies and programmes throughout the EU. In accordance with the priorities set by the European Parliament and the Council in the multi-annual financial framework (MFF), the European Commission carries out specific programmes, activities and projects in the field with the technical support of some specialised agencies.
The consolidated annual accounts of the EU provide information on the activities of the institutions, agencies and other bodies of the EU from a budgetary and accrual accounting perspective.
The consolidated reports on the implementation of the general budget of the EU include the budget implementation of all Institutions. Agencies do not have a separate budget inside the EU budget ; and they are partially financed by a Commission budget subsidy.
This document sets out how the Agencies spent and implemented their budget in 2014. Each agency is subject to its own discharge procedure.
EMEA : in 2014, the tasks and budget of this agency were as follows:
description of the Agency's tasks : the European Medicines Agency, which is located in London (UK), was created by Council Regulation (EEC) No 2309/93 , which was replaced by Regulation (EC) No 726/2004 of the European Parliament and of the Council and its role is the coordination of the scientific resources made available by the national authorities in order to ensure the evaluation and supervision of medicinal products for human or veterinary use on the basis of a centralised procedure; the Agency's budget for the 2014 financial year : the Agency’s budget for 2014, as presented in the Commission document on the consolidated annual accounts of the European Union, gives the following figures:
Commitment appropriations :
- committed : EUR 282 million;
- paid : EUR 266 million;
- carried over : 0.
Payment appropriations :
- committed : EUR 316 million;
- paid : EUR 251 million;
- carried over : EUR 47 million.
See also the final accounts of the EMA.
PURPOSE: presentation by the Commission of the consolidated annual accounts of the European Union for the financial year 2014, as part of the 2014 discharge procedure.
Analysis of the accounts of the European Medicines Agency (EMEA) .
CONTENT: this Commission document sets out the consolidated annual accounts of the European Union for the financial year 2014 as prepared on the basis of the information presented by the institutions, organisations and bodies of the EU, in accordance with Article 148 (2) of the Financial Regulation applicable to the EU's General Budget, including the European Medicines Agency (EMEA).
The document contains the figures on which the discharge procedure is based.
On this basis, the Financial Controller of the European Commission ensures the certification of the consolidated accounts as declared by the institutions, agencies and bodies of the European Union.
Discharge procedure of the EU agencies : the EU Budget finances a wide range of policies and programmes throughout the EU. In accordance with the priorities set by the European Parliament and the Council in the multi-annual financial framework (MFF), the European Commission carries out specific programmes, activities and projects in the field with the technical support of some specialised agencies.
The consolidated annual accounts of the EU provide information on the activities of the institutions, agencies and other bodies of the EU from a budgetary and accrual accounting perspective.
The consolidated reports on the implementation of the general budget of the EU include the budget implementation of all Institutions. Agencies do not have a separate budget inside the EU budget ; and they are partially financed by a Commission budget subsidy.
This document sets out how the Agencies spent and implemented their budget in 2014. Each agency is subject to its own discharge procedure.
EMEA : in 2014, the tasks and budget of this agency were as follows:
description of the Agency's tasks : the European Medicines Agency, which is located in London (UK), was created by Council Regulation (EEC) No 2309/93 , which was replaced by Regulation (EC) No 726/2004 of the European Parliament and of the Council and its role is the coordination of the scientific resources made available by the national authorities in order to ensure the evaluation and supervision of medicinal products for human or veterinary use on the basis of a centralised procedure; the Agency's budget for the 2014 financial year : the Agency’s budget for 2014, as presented in the Commission document on the consolidated annual accounts of the European Union, gives the following figures:
Commitment appropriations :
- committed : EUR 282 million;
- paid : EUR 266 million;
- carried over : 0.
Payment appropriations :
- committed : EUR 316 million;
- paid : EUR 251 million;
- carried over : EUR 47 million.
See also the final accounts of the EMA.
Documents
- Results of vote in Parliament: Results of vote in Parliament
- Decision by Parliament: T8-0176/2016
- Debate in Parliament: Debate in Parliament
- Committee report tabled for plenary: A8-0114/2016
- Amendments tabled in committee: PE576.947
- Supplementary non-legislative basic document: 05584/2016
- Committee draft report: PE569.754
- Committee opinion: PE571.772
- Court of Auditors: opinion, report: OJ C 409 09.12.2015, p. 0197
- Court of Auditors: opinion, report: N8-0137/2015
- Non-legislative basic document: COM(2015)0377
- Non-legislative basic document: EUR-Lex
- Non-legislative basic document published: COM(2015)0377
- Non-legislative basic document published: EUR-Lex
- Non-legislative basic document: COM(2015)0377 EUR-Lex
- Court of Auditors: opinion, report: OJ C 409 09.12.2015, p. 0197 N8-0137/2015
- Committee opinion: PE571.772
- Committee draft report: PE569.754
- Supplementary non-legislative basic document: 05584/2016
- Amendments tabled in committee: PE576.947
Activities
- Marina ALBIOL GUZMÁN
Plenary Speeches (1)
- Jean ARTHUIS
Plenary Speeches (1)
- Marie-Christine ARNAUTU
Plenary Speeches (1)
- Jonathan ARNOTT
Plenary Speeches (1)
- Zoltán BALCZÓ
Plenary Speeches (1)
- Zigmantas BALČYTIS
Plenary Speeches (1)
- Hugues BAYET
Plenary Speeches (1)
- Xabier BENITO ZILUAGA
Plenary Speeches (1)
- José BLANCO LÓPEZ
Plenary Speeches (1)
- Renata BRIANO
Plenary Speeches (1)
- Steeve BRIOIS
Plenary Speeches (1)
- Gianluca BUONANNO
Plenary Speeches (1)
- James CARVER
Plenary Speeches (1)
- Nicola CAPUTO
Plenary Speeches (1)
- Alberto CIRIO
Plenary Speeches (1)
- Therese COMODINI CACHIA
Plenary Speeches (1)
- Andi CRISTEA
Plenary Speeches (1)
- Daniel DALTON
Plenary Speeches (1)
- Michel DANTIN
Plenary Speeches (1)
- William (The Earl of) DARTMOUTH
Plenary Speeches (1)
- Mireille D'ORNANO
Plenary Speeches (1)
- Norbert ERDŐS
Plenary Speeches (1)
- Edouard FERRAND
Plenary Speeches (1)
- Doru-Claudian FRUNZULICĂ
Plenary Speeches (1)
- Ildikó GÁLL-PELCZ
Plenary Speeches (1)
- Arne GERICKE
Plenary Speeches (1)
- Sylvie GODDYN
Plenary Speeches (1)
- Tania GONZÁLEZ PEÑAS
Plenary Speeches (1)
- Takis HADJIGEORGIOU
Plenary Speeches (1)
- Brian HAYES
Plenary Speeches (1)
- Marian HARKIN
Plenary Speeches (1)
- Cătălin Sorin IVAN
Plenary Speeches (1)
- Diane JAMES
Plenary Speeches (1)
- Ivan JAKOVČIĆ
Plenary Speeches (1)
- Philippe JUVIN
Plenary Speeches (1)
- Barbara KAPPEL
Plenary Speeches (1)
- Afzal KHAN
Plenary Speeches (1)
- Bernd KÖLMEL
Plenary Speeches (1)
- Giovanni LA VIA
Plenary Speeches (1)
- Marine LE PEN
Plenary Speeches (1)
- Bernd LUCKE
Plenary Speeches (1)
- Ivana MALETIĆ
Plenary Speeches (1)
- Andrejs MAMIKINS
Plenary Speeches (1)
- Dominique MARTIN
Plenary Speeches (1)
- Notis MARIAS
Plenary Speeches (1)
- Jean-Luc MÉLENCHON
Plenary Speeches (1)
- Marlene MIZZI
Plenary Speeches (1)
- Sophie MONTEL
Plenary Speeches (1)
- Renaud MUSELIER
Plenary Speeches (1)
- Liadh NÍ RIADA
Plenary Speeches (1)
- Florian PHILIPPOT
Plenary Speeches (1)
- Marijana PETIR
Plenary Speeches (1)
- Franck PROUST
Plenary Speeches (1)
- Julia REID
Plenary Speeches (1)
- Claude ROLIN
Plenary Speeches (1)
- Lola SÁNCHEZ CALDENTEY
Plenary Speeches (1)
- Maria Lidia SENRA RODRÍGUEZ
Plenary Speeches (1)
- Siôn SIMON
Plenary Speeches (1)
- Monika SMOLKOVÁ
Plenary Speeches (1)
- Davor ŠKRLEC
Plenary Speeches (1)
- Igor ŠOLTES
Plenary Speeches (1)
- Joachim STARBATTY
Plenary Speeches (1)
- Beatrix von STORCH
Plenary Speeches (1)
- Patricija ŠULIN
Plenary Speeches (1)
- Tibor SZANYI
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- Dubravka ŠUICA
Plenary Speeches (1)
- Pavel TELIČKA
Plenary Speeches (1)
- Miguel VIEGAS
Plenary Speeches (1)
Votes
A8-0114/2016 - Derek Vaughan - Résolution #
Amendments | Dossier |
21 |
2015/2171(DEC)
2015/12/22
ENVI
5 amendments...
Amendment 1 #
Draft opinion Paragraph 3 a (new) 3a. Welcomes that a new procedure entered into force in 2014 which corrected the former irregular practice, whereby the Agency paid education contributions directly to schools for staff, in contravention of the Staff Regulations;
Amendment 2 #
Draft opinion Paragraph 8 8. Reiterates the important role of the Agency in protecting and promoting
Amendment 3 #
Draft opinion Paragraph 8 8. Reiterates the important role of the Agency in protecting and promoting public and animal health by assessing and supervising medicines for human or veterinary use; notes the publication, in November 2014, of the Agency's revised policy on the handling of declarations of interests by scientific committee members and experts, and welcomes that the revisions reflect a more balanced approach to handling declarations of interests, and aim to effectively restrict the involvement of experts with possible conflicts of interests in the Agency’s work, while maintaining the Agency's ability to access the best available expertise; stresses that the Agency should ensure maximum transparency in providing access to clinical reports, and welcomes the Agency's decision proactively to publish data on clinical trials; considers that businesses should not be allowed to evade the obligation to communicate such data on the basis of potential risk to commercial interests;
Amendment 4 #
Draft opinion Paragraph 9 9. Notes with concern that, despite the Agency’s fee regulation2 providing due
Amendment 5 #
Draft opinion Paragraph 9 a (new) 9a. Is therefore extremely concerned that despite the identified weakness in the functioning of pharmacovigilance, the Agency launched in March 2014 a pilot project on adaptive licencing - endorsed neither by the Parliament nor by the Council, as implementing adaptive pathways would shift the burden of evidence from pre-marketing to post- marketing, leading to a situation where premature marketing authorisations could become the rule, therefore putting Union citizens' health unnecessarily at risk;
source: 573.130
2016/03/04
CONT
16 amendments...
Amendment 1 #
Proposal for a decision 1 Paragraph 1 1.
Amendment 10 #
Motion for a resolution Paragraph 8 a (new) 8a. Encourages the EU institutions and agencies to better raise awareness of the conflict-of-interest policy among their officials, alongside ongoing awareness- raising activities and the inclusion of integrity and transparency as an obligatory item to be discussed during recruitment procedures and performance reviews; considers that a distinction should be made between elected representatives and public officials in the legislation on conflicts of interest; believes that there should also be such regulations in the Member States for public officials and civil servants involved in the administration and monitoring of EU subsidies; calls on the Commission to submit a draft legal basis on this matter;
Amendment 11 #
Motion for a resolution Paragraph 11 a (new) 11a. Calls for an overall improvement in the prevention of, and the fight against, corruption in the public sector, and especially within the EU institutions and agencies, through a holistic approach, commencing with better public access to documents and more stringent rules on conflicts of interest, the introduction or strengthening of transparency registers and the provision of sufficient resources for law enforcement measures, and also through improved cooperation among Member States and with relevant third countries;
Amendment 12 #
Motion for a resolution Paragraph 11 b (new) 11b. Calls on all the EU institutions and agencies to enhance their procedures and practices aimed at safeguarding the financial interests of the Union and to actively contribute to a results-oriented discharge process;
Amendment 13 #
Motion for a resolution Paragraph 12 a (new) 12a. Is extremely concerned that despite the identified weakness in the functioning of pharmacovigilance, the Agency launched in March 2014 a pilot project on adaptive licencing - endorsed neither by the Parliament nor by the Council, as implementing adaptive pathways would shift the burden of evidence from pre- marketing to post-marketing, leading to a situation where premature marketing authorisations could become the rule;
Amendment 14 #
Motion for a resolution Paragraph 12 a (new) 12a. Demands that all those EU institutions and agencies that have not yet done so urgently adopt internal rules on whistleblowing and take a common approach to their obligations, focusing on the protection of whistleblowers; requests special attention for the protection of whistleblowers in the context of the Directive on the Protection of Trade Secrets; calls on the Commission to promote legislation on a minimum level of protection for whistleblowers in the EU; calls on the institutions and agencies to amend the Staff Regulations to ensure that they not only formally oblige officials to report irregularities of all kinds but also lay down adequate protection for whistleblowers; calls on the institutions and agencies to implement Article 22(c) of the Staff Regulations without delay;
Amendment 15 #
Motion for a resolution Paragraph 13 13. Takes note that in 2014, the Agency carried out an administrative procedure
Amendment 16 #
Motion for a resolution Paragraph 13 13. Takes note that in 2014, the Agency carried out an administrative procedure
Amendment 2 #
Proposal for a decision 1 Paragraph 1 1.
Amendment 3 #
Proposal for a decision 2 Paragraph 2 2.
Amendment 4 #
Proposal for a decision 2 Paragraph 2 2.
Amendment 5 #
Motion for a resolution Paragraph 2 2. Notes from the Court’s report that the Agency’s Fee Regulation13 provides due dates for the collection of fees from applicants and the Agency’s related payments to national competent authorities; notes that these due dates were not respected for most of the transactions audited by the Court; ascertains from the Agency that it has redesigned and streamlined its main operational processes including financial authorisations and fee collections; takes note that the further automation of these processes was planned to be implemented by the Agency by the end of 2015; calls on the Agency to take all further steps needed in order to ensure that its pharmacovigilance responsibilities are fully met and to effectively report to the discharge authority on measures implemented to remedy this issue;
Amendment 6 #
Motion for a resolution Paragraph 3 3. Notes that budget monitoring efforts during the financial year 2014 resulted in a budget implementation rate of 94,32 %
Amendment 7 #
Motion for a resolution Paragraph 5 a (new) 5a. Calls on the Agency as far as possible to reduce the level of committed appropriations carried over in the future in order to strengthen transparency and accountability;
Amendment 8 #
Motion for a resolution Paragraph 7 7. Takes note from the Agency that, in order to increase the level of human resources allocated to operational tasks, it is further improving its recruitment and resource planning procedures; ascertains from the Court's Report that in 2014 the Agency concluded an EUR 15 000 000 framework contract for high-level management consultancy services covering the 2014-2017 period; notes that the objectives and activities to be carried out were not sufficiently specific to justify the procurement decision or the volume of the contract; calls on the Agency therefore, in the interests of transparency and accountability, to ensure that the objectives and activities to be carried out are in fact specified; notes furthermore that the Court found no evidence that the Agency’s Management Board had been consulted on the procurement decision; acknowledges from the Agency that consulting its Management Board in this case was not required by the financial rules;
Amendment 9 #
Motion for a resolution Paragraph 7 a (new) 7a. Asks the EU institutions and bodies to apply strictly the measures pertaining to discretion and exclusion in respect of public procurement, with proper background checks being carried out in every instance, and to apply the exclusion criteria in order to debar companies in the event of any conflict of interest, this being essential to protect the EU's financial interests;
source: 576.947
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