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Best practice guide on measures improving predictability of submissions/ responses and adherence to communicated submission/ responses deadlines Presentation of Revised BPG after Consultation with Industry to Committees and CMDs June 2017 An


  1. Best practice guide on measures improving predictability of submissions/ responses and adherence to communicated submission/ responses deadlines Presentation of Revised BPG after Consultation with Industry to Committees and CMDs June 2017 An agency of the European Union

  2. Aim of this presentation Present the Best Practice Guide as developed by the HMA TaskForce Inform about the outcome of the public consultation Inform about the next steps Final Best practice guide presentation to Committees / CMDs 1

  3. Background Task Force started in 2013 Why ? • Limited resources in evaluation units • Important to allocate staff according to timelines set • Changing timelines is challenging • Especially around big bank holidays and the summer break • All procedures need the same resources Final Best practice guide presentation to Committees / CMDs 2

  4. Aim of the Best Practice Guide (BPG) Common issues  The BPG covers CP/ DCP/ MRP/ national procedures, Human and Vet For I nitial MAAs The aim is to agree with Industry on principles that will ensure Predictability Good communication This is a start, a lot of issues remain to be solved… … .. Final Best practice guide presentation to Committees / CMDs 3

  5. Steps in development of the Best Practice Guide Workshop with Industry in April 2016 Consultation with Industry associations in February 2017 Comments received by March 2017 Final Best practice guide presentation to Committees / CMDs 4

  6. Main recommendations of the BPG Pre-subm ission phase- Em phasis on Com m unication Maintained • Submission dates to be re-confirmed 2-3 months prior to the intended submission • Engagement in early dialogue with the EMA/ NCAs is encouraged • Emphasize the importance of mature dossiers If an intended submission date is not met  discussion with EMA/ NCAs to assure the • availability of assessment teams and adjustment of the submission date, if needed. • Early appointment of contact points and Rapporteurs • Transparent procedures for booking slots • Final Best practice guide presentation to Committees / CMDs 5

  7. Main recommendations of the BPG Responses to LoQ/ LoOI - I ndustry Maintained Responses submission date  Upon receipt of the preliminary ARs and confirmed • within 2 weeks after receipt of the final LoQ/ LoOI. If submission date is not met  discussion with EMA/ NCAs to assure the availability • of assessment teams and adjustment of the procedural TT • Extension of the clock-stop to be discussed as soon as possible • Clarification meetings to focus on clarification of questions / discussion on the applicant’s approach to respond NOT pre-assessment . 6 Final Best practice guide presentation to Committees / CMDs

  8. Main recommendations of the BPG Responses to LoQ/ LoOI - Regulators Very Important • Timely circulation of (preliminary/ draft ) ARs and Comments for Industry • Questions in the ARs are clear and unambiguous • Late questions/ SmPC changes after adoption of LoQs/ LoOIs to be avoided • Clarifications to questions to be provided timely Final Best practice guide presentation to Committees / CMDs 7

  9. Next steps Presentation to Committees ( CHMP/ CVMP) and CMDs in June 2017 Revised BPG and responses to comments to be shared with Industry in July 2017 Adoption at HMA September meeting Publication of the BPG on HMA and HMA websites Final Best practice guide presentation to Committees / CMDs 8

  10. Thank you for your attention

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