EU28: Science, Medicines, Health A regulatory system fit ...€¦ · EU28: Science, Medicines,...
Transcript of EU28: Science, Medicines, Health A regulatory system fit ...€¦ · EU28: Science, Medicines,...
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EU28: Science, Medicines, Health A regulatory system fit for the future Session: Going Digital Presentation: Current Initiatives Presented by: Andrea Johnson (MHRA), Olivier Simoen (EMA) Version 01.01
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Current initiatives
Objective of the presentation:
Provide an overview of the current initiatives in digital provision of electronic information within the EU Medicines Regulatory Network
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Contents
• General principles
• Short term initiatives
• Medium term initiatives
• Long term initiatives
• MHRA-specific initiatives
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Sharing and
easier access
General Principles (1/5):
Provide data once
More structured data
Increased turn-around time
One single entry point
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Collaboration
Process
Standardisation
Data V
ision
Four driving forces:
Increase the sharing of
data across the network
Simplify provision of
data
Increase (even more)
the collaboration across the network
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General Principles (2/5): Challenges for integration and collaboration in Europe:
Processes vary
Industry NCAs National
Industry
EMA
NCAs
Centralised
Industry
NCAs
De-Centralised
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General Principles (3/5):
Size is strength… …the chain is only as good as the weakest link
…but…
The EU regulatory environment
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How do we effectively share?
General Principles (4/5):
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Options • Collaborate across EU • Tactical collaborations
• Go Commercial…
What do each of these look like and when are
they planned for?
General Principles (5/5):
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Short term (next few months) (1/7):
• Next version of MAA H eAF implementing AF V10: June 13
• Pilot electronic submission of CT results (Pilot 2): June 13
• Pilot esignatures of EMA forms: Q3 13
• Initially in the area of orphan drugs, paediatrics and scientific advise
• Set of forms to be extended next
• Electronic submission of GMDP (V 5) information: May 13
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Short term (next few months) (2/7): • Implementation of the new EU Telematics governance
structure: Q2 13
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Coo
rdin
atio
n
EMA MB incl. EC HMA
EU Telematics Management Board
IT Directors meeting
IT Directors Executive Group for Telematics
Telematics EA Board
Support
Projects and maintenance
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Short term (next few months) (3/7):
• CESP – A portal for Europe
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Short term (next few months) (4/7): • CESP -Overview of Activities:
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Short term (next few months) (5/7):
Registration Server
Agency C File Transfer Server
Industry User
User logs on to registration server and
creates delivery file
User downloads delivery
file to local PC
User uploads submission and
delivery file to FTP server
Files are moved to agency servers
Agency A
Agency B
• CESP - Current operation:
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Short term (next few months) (6/7): • CESP - general statistics: November 2012 to March 2013:
• Number of weeks in operation : 21
• Number of registered companies : 420
• Total number of submissions delivered : 9259
• Largest submission to date : 8Gb to 18 agencies
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Short term (next few months) (7/7):
• Falsified Medicines Directive (FMD)
• Initiative to look at Broker Registrations across Europe
• Spanish and UK are leading on this initiative working with other interested MS
• Concept: • XML forms
• Central data repository for MS interrogation
• Possible EMA involvement
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Medium term (one year from here) (1/2): • Introduction of esignatures of more EMA forms
• EU Medicines web portal
• Electronic submission of updates of product information according to art 57 (of Reg 2012/1235)
• Common Repository: Access for NCAs to CAP MAA info
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Medium term (one year from here) (2/2): • International standards:
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ICSR
IDMP
CTR&R
eCTD 4
ePSUR &
eRMP
…
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Long term (1/3):
Submissions can be loaded directly into CESP, all
responses and requests come back via CESP
International and EU vocabularies and dictionaries
An option for industry to build eCTDs directly in
CESP
Agency can download
submissions, upload tracking information and
RFI Data
European systems can provide and receive
information
• CESP medium-to-long term initial vision:
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Long term (next few years) (2/3): • Common Repository should contain also PSURs, RMPs and
MRP/DCP submissions
• Integration CESP and EMA eSub GW
• EU Medicines Submission Portal should:
• Combine CESP and eSubmission Website
• Be published by EMA and HMA
• Allow Submission of National Procedure, MRP/DCP, Centralised Procedure Applications
• Contain information on all subjects: Submission, eAF, eCTD Standards, etc.
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Long term (next few years) (3/3): • Use of RPS (eCTD 4) for esubmission of MAA information
• Completion of EMA Online strategy: New B2B portal; EU Medicines Web portal; New extranet for extended collaboration with NCAs
• Implementation of EMA Data Architecture roadmap (tier 1)
• eSubmission vision
• One submission mechanism, entry point, process, output
• “The ultimate aim of eSubmission is full dematerialisation of the exchange of regulatory information between applicants and the Network and between regulatory authorities within the Network, enabling electronic collaborative processes and transparency throughout the medicinal product life-cycle. “
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Options for effectively sharing • Collaborate across EU
• TACTICAL COLLABORATIONS • Go Commercial…
MHRA-Specific Initiatives (1/5):
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MHRA Medicines IT strategy developed in 2002 and implemented 2003-6 as the system
Key principles • transparency of data
across business processes
• Electronic information is the master
MHRA-Specific Initiatives (2/5):
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MHRA-Specific Initiatives (3/5):
RedAnt
Danish E-Forms
MHRA Yellowcard
RedAnt
Windows
Sharing Short-long term
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Options for effectively sharing • Collaborate across EU
• Tactical collaborations
• Go Commercial…
MHRA-Specific Initiatives (4/5):
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Medium to Long term – Risk Based Inspections MHRA-Specific Initiatives (5/5):
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Thank you
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