Standard operating procedure Title: Requesting exceptions and recording of non-compliance events Status: PUBLIC Document no.: SOP/EMA/0044 Lead author Approver Effective date: 28-JUL-2014 Name: Mario Benetti Name: Guido Rasi Review date: 28-JUL-2017 Signature: On file Signature: On file Supersedes: SOP/EMA/0044 (19-MAY-11) TW3280 Date: 25-JUL-2014 Date: 25-JUL-2014 TrackWise record no.: 4037 1. Purpose The procedure describes the approval, registration and follow up of exceptions and/or non-compliance events as in accordance with the standard for internal control on recording exceptions (standard No. 8), the Agency shall ‘[….] track and give prior approval to control overrides or deviations from policies and procedures. The aim of reporting exception and/or non-compliance is to ensure that any deviation from established policies or procedures is documented, justified and approved at an appropriate level before decision/action is taken. 2. Scope The procedure is applicable to all Agency staff through the hierarchy. This procedure is without prejudice to the one described in the charter of tasks and responsibilities of the verifying officer and verifying assistant(s) in paragraph 6.7 to 6.9 (doc. no.: EMEA/11970/59). The present procedure does not cover irregular activities which are described in a separate procedure dealing with reporting suspected improprieties (EMEA/11591/2006/2320). 3. Responsibilities It is the responsibility of the Executive Director, Heads of Division and Department, Authorising Officers by delegation/sub-delegation to ensure that staff is aware of and complies with this procedure. Specific responsibilities are outlined in section 9. 30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 Send a question via our website www.ema.europa.eu/contact An agency of the European Union © European Medicines Agency, 2015. Reproduction is authorised provided the source is acknowledged. 4. Changes since last revision Update of SOP title to include “non-compliance” Updated reference to the Charter of responsibilities of the verifying officer and verifying assistant(s) Rename of managerial titles following the reorganisation/restructuring Review the steps and description of the procedure Update the request for an exception form (Annex I) 5. Documents needed for this SOP Register of exceptions (Cabinets/06. Corporate governance/06.2 Integrated Management System/6. Internal controls/Exceptions) Template for requesting an exception (Word-File-New-Templates-Agency-More-request for exception) 6. Related documents Standards for internal control (EMA/MB/555181/2010) 7. Definitions ED: Executive Director AO: Authorising officer by delegation/ sub-delegation HDiv: Head(s) of Division HDep: Head(s) of Department ED-CG: Corporate Governance Department ED-CG-QRM: Quality assurance, Risk Management and ex-post control coordination function A-FI-VFO: Verification Office RAP: Rules of application Exception: 1. It constitutes a deviation from established processes and procedures (action of replacing one or more steps in established process/procedures with another action or no action) or, an overriding of controls (action which goes against the results of previous controls) but does not constitute a breach of regulatory and/or contractual provisions and, 2. It is not foreseen in already existing processes/procedures and, 3. It is approved by the responsible person before action is taken (ex ante) Non-compliance: 1. It constitutes a deviation from established processes and procedures or an overriding of controls or a gap in existing controls and, 2. It might entail a breach of existing regulatory and/or contractual provisions, and Standard operating procedure - PUBLIC SOP/EMA/0044, 28-JUL-2014 Page 2/9 3. It is detected after action was taken (ex post). Regulatory provisions (e.g. regulation, directive, Financial Regulation, Implementing Rules, Rules of application, Staff Regulations, data protection regulation, access to documents) Contractual provisions (e.g. contracts with entities outside of the European Medicines Agency) Procedures (e.g. internal implementing rules, manuals, guidelines, SOPs, WINs…) Standard operating procedure - PUBLIC SOP/EMA/0044, 28-JUL-2014 Page 3/9 8. Process map(s)/ flow chart(s) Start 1. Complete template and forward it to Head of Division 2. Head of Division or delegated Authorising Officer validates/rejects the request after consultation with A-FIVFO and ED-CG-QRM Rejected validated 4. Head of Division or delegated Authorising Office forward the validated request to ED-CG 3. Notify originator of rejection and advise on alternative course of action 5. ED-CG obtain decision of Executive Director 6. Notify Head of Division or delegated Authorising Officer to proceed in accordance with decision taken by ED 7. Register the exception/ non-compliance together with the decisions taken End Standard operating procedure - PUBLIC SOP/EMA/0044, 28-JUL-2014 Page 4/9 9. Procedure Step Action Responsibility 1. Request an exception or report a non-compliance event by Staff member completing a request form (Annex I) and forward it to Head of initiating the Division for validation. The request should: request Indicate which regulatory and/or contractual provisions, policy/procedure/regulation/process is not respected. Describe the type of transaction/event and amount concerned. Explain the exceptional circumstances that justify an exception request or that caused a non-compliance. Describe the risk (e.g. reputational, financial or legal). Indicate the actions taken to mitigate the resulting risk and/or measures proposed to avoid repetition of the situation. 2 Validate/reject the request after consulting with the Verification Head of Division / office (A-FI-VFO) and the Quality assurance and risk management Authorising Officer function (ED-CG-QRM) (by delegation / sub- If the request is rejected go to step 3. delegation) If the request is validated go to step 4. 3 Inform staff member of decision and advise on alternative course Head of Division / of action Authorising Officer (by delegation / subdelegation) 4 Head of Division or delegated Authorising Officer forward the Head of Division / validated request to ED-CG. Authorising Officer (by delegation / subdelegation) 5 Obtain decision from the Executive Director ED-CG-QRM 6 Notify Head of Division or delegated Authorising Officer to proceed ED-CG-QRM in accordance with decision taken by ED 7 Register the decision taken and file original request. Standard operating procedure - PUBLIC SOP/EMA/0044, 28-JUL-2014 ED-CG-QRM Page 5/9 10. Records Electronic files: The register of exceptions/non-compliances, including the completed forms and the supportive documentation, are kept in the appropriately labelled folder in the electronic document management system: Cabinets/06. Corporate governance/06.2 Integrated Management System/6. Internal controls/Exceptions Document security setting: For non-confidential documents the ACL EMA_default_staffonly should be used. For confidential issues an ACL with an appropriate access level should be chosen. Signed originals: Originals of signed forms are kept by the Corporate Governance Office Department (ED-CG) Standard operating procedure - PUBLIC SOP/EMA/0044, 28-JUL-2014 Page 6/9 ANNEX 1 Request for an exception / reporting of non-compliance event CONFIDENTIAL (To be delivered by hand) URGENT Please call requester and inform of decision by (DD/MM/YYYY) (For non-urgent requests, information will be processed within 24 hours after decision) Exception Division: Non-compliance event Name: Office: Tel: Policy or procedure this request for exception/report of non-compliance refers to / is in conflict with (enclose reference)1: Financial Regulations /Staff Regulation/Implementing Rules/Legal base Contract / Grant Agreement Call for tenders / call for proposals Other (please specify) Type of transaction/event and amount concerned2 Exceptional circumstances that require an exception request / caused a non-compliance event Resulting risk of the exception / non-compliance (consequences of the event) Measures to be taken to mitigate the resulting risks and ensure that such a situation does not reoccur: Validation Opinion of the verification office (A-FI-VFO): Opinion of the quality assurance and risk management function (ED-CG-QRM): Head of Division or delegated Authorising Officer validates the application: Yes Date: .......................................................... No Signature: ................................................................ 1 To attach the relevant documents In case the amount cannot be determined or if the impact is not financial please indicate the significance e.g. important / immaterial 2 Request for an exception / reporting of non-compliance event - PUBLIC SOP/EMA/0044, 28-JUL-2014 Page 7/9 Decision Opinion of the Executive Director: Granted Date: .......................................................... Refused Signature: ................................................................ Justification if refusing request or if granting exception to regulatory or contractual obligations: Registration - For exception and non-compliance Reference Number: Date of registration in exceptions register by Internal Control Coordinator (ED-CG-QRM): Date: .......................................................... Signature: ................................................................ Request for an exception / reporting of non-compliance event - PUBLIC SOP/EMA/0044, 28-JUL-2014 Page 8/9 ANNEX 2 DELIVER BY HAND Transmission slip Request for exceptions and recording of non-compliance URGENT Please call requester and inform of decision by (DD/MM/YYYY) (For non-urgent requests, information will be processed within 24 hours after decision) Exception Non-compliance event Title/ brief description Transmission Name Signature Date Office / Tel. No. Initiator Head of Division A-FI-VFO ED-CG-QRM Head of Division / / / / / After consultation with A-FI-VFO and ED-CG-QRM the Head of Division validates the request and send it to the Executive Director for decision. ED-CG-QRM Executive Director ED-CG-QRM / / / Return to Initiator Initiator / Comments The transmission is effective on 15-JUL-2014. Please refer to SOP/EMA/0044 for details of the procedure. DELIVER BY HAND - PUBLIC SOP/EMA/0044, 28-JUL-2014 Page 9/9