BROMI Variations Training Meeting 8 May 2008 BROMI Variations – Training Presentation BROMI Variations Training Meeting, 8 th May 2008, The Cumberland.

Slides:



Advertisements
Similar presentations
1 Future strategy for e-submission as seen by industry Dr Michael Colmorgen, IFAH-Europe 2nd Veterinary Workshop on E-submission 4 Dec 2009, EMEA, London.
Advertisements

1 Harmonisation of requirements: where we are Erik Waterdrinker, IFAH-Europe 2nd Veterinary Workshop on E-submission 4 Dec 2009, EMEA, London.
European Union Cohesion Policy
Ethics – where to start! October 2013 Lois Neal FMS Research & Innovation Office.
Making Grants.gov Work for You: U.S. Department of Education Jacob K. Javits Gifted and Talented Students Education Program CFDA #84.206A Find. Apply.
Regulators’ Code July Regulators’ Code A statutory Code Came into effect in April 2014, replacing the Regulators’ Compliance Code All local authorities.
Safeguarding public health © Crown copyright 2008 BROMI eSubmissions Case study using the MHRA Portal : Tesfa Rodway – Information Systems Training Officer.
Key Action 1 for Schools Application advice - What the Assessor is looking for.
© Safeguarding public health BROMI Variations ·Launch Meeting The Cumberland Hotel, London Anne Ambrose 8 th May 2008.
BROMI Variations – An Industry Perspective
BROMI Variations Training Meeting 8th May 2008 Case Study Session BROMI VARIATIONS.
Water Ski Scoring Publishing Live Results Calculator Overview Publishing Live Results Calculator Overview.
New York State’s Teacher and Principal Evaluation System VOLUME I: NYSED APPR PLAN SUBMISSION “TIPS”
CareCentrix Direct Training.
The New TNI Laboratory Accreditation Standards Requirements for an Accreditation Body.
Mobile Marketing in Practice
1 Certification Chapter 14, Storey. 2 Topics  What is certification?  Various forms of certification  The process of system certification (the planning.
ISO 9001 Interpretation : Exclusions
EXCiPACT TM Certification 3rd Party Certification for Pharmaceutical Excipient Suppliers EFCG Update at CPhI, 9 th October 2012 Frithjof Holtz, Merck KGaA.
Access is Via Staffnet. Access You log onto the staff portal to access the program.
Responding to Inspection Findings
The Project AH Computing. Functional Requirements  What the product must do!  Examples attractive welcome screen all options available as clickable.
FDA Recalls Risk Communication Advisory Committee David K. Elder Director, Office of Enforcement.
Effectively applying ISO9001:2000 clauses 5 and 8
London Grid for Learning schools conference 30th april 2012.
CONTRACTUAL FLOW DOWN OF DPAS PRIORITY RATINGS
IB Internal Assessment Design. Designing an Experiment Formulate a research question. Read the background theory. Decide on the equipment you will need.
FPDS- NG Reports Overview December 16, Today’s Goals Provide an overview of the FPDS-NG reporting capability Demonstrate each of the reporting tools.
Electronic Banking Risk Assessment - Product Training
Welcome to BLT Online NQT Induction. Points We Will Cover: What is BLT Online NQT Service? What are the advantages of using it? User roles on the site.
CO2403 and CO3808 – Quality Management Systems Quality process definition, administration and accreditation.
Implementation of the Essential Standards The Australian Quality Framework (AQTF) is the national set of standards which assures nationally consistent,
CONFIDENTIAL ©2014 PAREXEL INTERNATIONAL CORP. ALL RIGHTS RESERVED. THE PRACTICE OF REGULATORY INTELLIGENCE: CASE STUDIES OMICS 5 th International Pharmaceutical.
Exam Taking Kinds of Tests and Test Taking Strategies.
Access to HE internal moderation and standardisation planning Workshop Session.
Important informations
Ivowen Ltd1 Ivowen Limited Preparation and Submission of a Traditional Herbal Medicinal Product Application.
New Regulation on Plant Reproductive Material: main elements of the upcoming Commission proposal Yannis Karamitsios European Commission, DG SANCO.
LECTURE 18 16/11/15. MAKING THE INTERFACE CONSISTENT Consistency is one way to develop and reinforce the users conceptual model of applications and give.
0 Electronic Subcontracting Reporting System (eSRS) Department of Defense Government Training Submitting a SSR – Commercial Plan.
MJAC Founded 1928 Contaminated Land Update 27 th March 2015 Worcester T
SAM-101 Standards and Evaluation. SAM-102 On security evaluations Users of secure systems need assurance that products they use are secure Users can:
FDA job description  Regulates about 25% of all consumer purchases  Mission summary: protect and advance public health  Products: food, cosmetics, drugs,
EN EUROPEAN COMMISSION Budgetary Control Committee of European Parliament Budgetary Control Committee of European Parliament Brian Gray DG BUDGET Workshop.
Accurate  Consistent  Compliant Contact: i4i the structured content company the structured content company.
A2 Agreement Trial ICT November AGENDA  New Specification Principal Moderator’s Report Exemplar Materials  Lunch  1.00 Exemplar Materials.
What is ISO Certification? Information is a valuable asset that can make or break your business. When properly managed it allows you to operate.
Variations regulation – an Industry experience
POST APPROVAL CHANGE MANAGEMENT PROTOCOLS IN THE EUROPEAN UNION
Understanding Standards: Nominee Training Event
Dr Pascale POUKENS-RENWART Scientific Officer
Information on Medicinal Products
EIA approval process, Management plan and Monitoring
Release Management Release Management.
Compliance Matters May 2013 Webinar – Bon Avis.
GMP Inspection Process
eSubmission Web Client XML delivery file – new functionality
Maintaining joint packaging and labelling into the future
Kasee Hildenbrand and Darcy Miller
CREATING A JOB REQUISITION
Professional support guides
Linda M. Chatwin, Esq. RAC Business Manager, UL LLC
Generic licensing guidelines
MAINTAINING THE INVESTIGATOR’S STUDY FILE
This presentation document has been prepared by Vault Intelligence Limited (“Vault") and is intended for off line demonstration, presentation and educational.
Recommendations to facilitate assessment of new application procedures
Variations and Mock-ups
Credit Accumulation Route
Getting Ready for IPMA Level D® Certification in the USA
This presentation document has been prepared by Vault Intelligence Limited (“Vault") and is intended for off line demonstration, presentation and educational.
Presentation transcript:

BROMI Variations Training Meeting 8 May 2008 BROMI Variations – Training Presentation BROMI Variations Training Meeting, 8 th May 2008, The Cumberland Hotel, London

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – What is it all about? Working within EU framework Expedited processing of certain categories Self-certification of certain Type IA changes Initiative available for portal submissions only Bulk applications can be made however only allowed for the same change over licences with the same marketing authorisation holder

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Key Benefits Freeing up assessors’ and industry’s time Responsibility of MAHs – risk based approach. Quicker and more predictable approval times for industry –Implementation requirements are the same as normal variation activities

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Available guidance MHRA guidance available ( –Based on EU guidance on dossier requirements for Type IA and Type IB Notifications –Colour coded to distinguish from EU guideline to help applicants identify if change they are applying for fits into scheme –Additional criteria for applications that are not assessed or validated company certifying acceptability of change

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Available guidance

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Hints & Tips Strategy –Changes should only relate to national marketing authorisations (No MRP, DCP or Centralised) –Know what change is required before you start; use the BROMI flow chart –Use flow charts decision making and deciding what category a particular change fits into. Also, use the variations guideline to help categorise the change –Think carefully about the categorisation/classification of simultaneous changes –Follow the BROMI variations checklist. If a condition / document is not applicable to the change being applied then it is not a BROMI. Don’t try to make it a BROMI when it isn’t!

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Hints & Tips

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Hints & Tips Document requirements –Define the changes clearly, and remain consistent throughout the documentation –Send the complete documentation package required by the guideline including the checklist but do not send anything unnecessary –Ensure any relevant additional documents (packaging components / label text / SmPC / dossier pages) are included with the application. Remember: If other additional component are impacted by the change but not explicitly referenced in the documentation requirements in the BROMI checklist, include them –Be clear & concise in your application - don’t presume the agency know what you mean, put yourself in their shoes!

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Hints & Tips Portal submission –The BROMI variations process uses portal applications only. –Add a sufficient description of the change in the scope box on the application form. –Choose the correct option on the application form including BROMI fees category –Use the comments section to add a description of the change, if the category doesn’t fit into the portal form.

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Hints & Tips Internal Company Processes –Create/develop your own internal procedures for submission AND FOLLOW THEM. BROMI puts the onus on the Company to get it right Example process guidance is in delegate packs –If there is time and resources available, have a brief internal quality check before submission.

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Pitfalls Pitfalls identified via pilot/audit activities Audit activity will still continue however there are consequences of not complying with the BROMI variation requirements. –Approval of application withdrawn –Enforcement action.

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Pitfalls Common reasons for invalid applications –Application not suitable for BROMI scheme –Wrong category chosen –Omission of key documents –Suitability of documentation and/or declarations –Omission of SPC, labels and leaflets –Multiple changes in one application

BROMI Variations Training Meeting 8 May 2008 BROMI Variations Launch – Pitfalls Pitfalls are easily avoided Seek advice if unsure MHRA contact details: or Regulatory Information Service Desk: