Data

5 - 6 October 2020

Location

Milan

Lingua

English

European Epidemiological Forum

Iscriviti
European Epidemiological Forum

The value of Real-World Evidence in Drug Life Cycle: promises, barriers and pathways to success


Regulators, health technology assessment (HTA) bodies, academics, bio-pharmaceuticals companies, payers, and patients are presently rethinking the healthcare ecosystem and facing diverse and increasing challenges at different levels. In this conceptual modelling of the healthcare ecosystem, the potential value of Real-World Data (RWD) for decision making has never been more relevant.
Real-World studies seek to provide complementary evidence to that provided by randomized controlled trials. While the latter provide evidence of efficacy, Real-World Data provide information on therapeutic effectiveness in a real-world practice setting.

Pharmaceutical companies need to focus on innovative and targeted therapies both due to the increased competition in the sector, and of the number of better structured and demanding patients’ groups or associations. Pharmaceutical companies are presently discussing on:

  • How does RWD contribute to translational research?
  • Whether there are any companies optimally leveraging RWD and how its application to biobanks can better advance innovation and discovery of targeted therapies?
  • What are the structural and logistical needs for this to be effective?
  • What have we already learned about the process?

Regulatory bodies face the challenge of ensuring that only safe and effective medicines reach patients; a decision which so far has only been substantiated upon data from RCTs. They actually need to know:

  • Whether other stakeholders can help them in the process and how?
  • Where and how do we using RWD in the drug development and approval process?
  • What has already been achieved in the field and what the success factors are? 


Payers, and HTA bodies want to make sure that the most innovative and novel medicines reach patients who need them most as quickly as possible; and that these medicines provide value for money to all parties: patients and health care systems. They may ask themselves:

  • How can sponsors better demonstrate the value of their innovative medicines using RWD?
    How can they work with decision-makers to establish agreed upon standards for RWE research?
    How do recent frameworks (FDA, NICE, etc) help advance RWE research?   


What brings all stakeholders at the same level is the need for new paradigms for a more performing healthcare ecosystem that reduce the gap between its representation and its implementation. Emerging e-health models and applications can greatly contribute to it, particularly, if hand-in-hand with Real-World Data Studies.

The European Epidemiological Forum will review the progress and perspectives on the value of RWD in the drug life cycle, will discuss what RWD promises, what the barriers may be and what a successful story may look like. 


Scientific Board:

Christian Agboton - Sr Global Brand Medical Director at Takeda
Maurille Feudjo Tepie - Observational Research Director at Amgen
Michele Intorcia - Health Economics Outcomes Research CoE Head at Vifor Pharma


Who should attend?

The conference is addressed to professionals with a deep interest in drug development, healthcare decision making, academia and healthcare research, belonging to department such as: Medical Affairs, R&D, HTA/Market access, Medical Informatics, Clinical Operations, Regulatory Affairs, Pharmacovigilance, Biostatistics and Data Management from Pharmaceutical, Biotechnology and Medical Device companies, CROs, Universities/Hospitals, Academic Research, Patient Associations and Healthcare Organizations.


For sponsorship opportunities, please contact events@lsacademy.com

Attestato di partecipazione

Certificate of attendance

5 October 2020 | PRE-CONFERENCE WORKSHOP

Half-Day Workshop 13:00 - 17:45


Design and Implementation of Real-World Evidence Methods to Deliver Value to Physicians and Payers

A workshop to learn and understand what RWE could bring that no other method can 


Introduction

You may have heard that Real-World Data (RWD) is the next big thing, but where do we start if we want to ride the wave of RWD driven change?
In order to be able to design and actually implement the specific tools and methodologies to collect Real-World Evidence (RWE), we first need to understand the benefits and limitations of these data. Knowing how both, clinicians and payers, make use of RWE helps us in defining appropriate scenarios and avoiding common pitfalls. Learn how to assess your success, change and implement a strategic plan!

Who should attend?

This workshop is aimed at people working in the pharmaceutical industry or in the related fields with an interest on practical aspects of real-world data collection and analysis. 


Programme

  • Introduction to RWE and objectives of the workshop
  • Designing a successful strategy both for Clinicians and Payers:  Preparing participants to use the toolbox
  • First group: Prepare your tactics to fill the gap for clinicians, and present them to the others
  • Second group: Prepare your tactics to convince payers, and present them to the others
  • Feedback from the trainers: what could be improved?
  • First group: Fine tune second group’s project. Second group: fine tune first group’s project
  • Lessons learned and conclusion

Language: The workshop will be in English


Agenda

13:00 - 13:30         Participants registration
13:30                      Course commences
15:15 - 15:30         Coffee break
17:30 - 17:45         Q&A and Conclusion

Teaching methods

The workshop is designed with a very pragmatic approach to implement real-world evidence strategies. This is an interactive training based on different scenarios. Participants will have to design and build an approach to collect and analyse Real-World Data under the supervision of the trainers.
Participants are kindly asked to bring their own computer/tablet.

Lecturers

Christian Agboton - Sr Global Brand Medical Director at Takeda
Christian J. Agboton currently serves as Senior Global Brand Medical Director at Takeda based in Zurich, Switzerland. He previously served as Medical Director of Biosimilars Immunology / inflammation at Sandoz and Hospira/Pfizer. Christian also worked at GSK vaccines, Merck Serono and UCB Pharma in Clinical and Medical Affairs roles. Channeling innovation to deliver evidence while keeping quality and timelines has always been at the heart of his approach to data generation. Christian is Fellow of the Royal Faculty of Pharmaceutical Medicine (FFPM).

Maurille Feudjo Tepie - Observational Research Director at Amgen
Dr. Maurille Feudjo Tepie is an Observational Research Director at Amgen and leads the Amgen European Team of the Centre for Observational Research. Prior to joining Amgen in 2009, he spent six years in the Worldwide Epidemiology Department at GSK. Maurille obtained his PhD in Medical Statistics from the London School of Hygiene and Tropical Medicine and then completed a one year post-doctoral fellowship working on a collaborative methodological project between the Worldwide Epidemiology Department of GSK and the London School of Hygiene and Tropical Medicine, under the supervision of Profs Stuart Pocock and Steven Evans. He has considerable experience designing and executing appropriate observational research strategies to inform drug development and drug commercialisation and; is a keen contributor to scientific discussions pertaining to the challenges and/or opportunities offered to regulators, payers, academics, prescribers and to the bio-pharmaceutical industry by advances in computing science and the increased availability of real world data. He has been active in European-wide initiatives aimed at improving biomedical research (IMI PROTECT and EMIF) and is also the chair of the PSI Epidemiology Special Interest Group.


At the end of the workshop, you will be able to: 

  • Design and use the tools specific to Real-World Evidence
  • Understand the benefits and limitations to Real-World Data
  • Use 2 different approaches (for physicians, and payers) gathering elements important to deliver your pre-established strategy
  • Avoid pitfalls by consulting experts and assessing you chances of success 

Maggiori informazioni disponibili a breve

Coordinatori Scientifici

Christian Agboton
Christian Agboton Sr Global Brand Medical Director at Takeda
Maurille  Feudjo Tepie
Maurille Feudjo Tepie Observational Research Director at Amgen
Michele Intorcia
Michele Intorcia Health Economics Outcomes Research (HEOR) CoE Head at Vifor Pharma

Maggiori informazioni disponibili a breve

Coordinatori Scientifici

Christian Agboton
Christian Agboton Sr Global Brand Medical Director at Takeda
Maurille  Feudjo Tepie
Maurille Feudjo Tepie Observational Research Director at Amgen
Michele Intorcia
Michele Intorcia Health Economics Outcomes Research (HEOR) CoE Head at Vifor Pharma

Sede della Conferenza

Novotel Milano Nord Ca Granda
Viale Suzzani 13, 20162 – Milano

Situated centrally, just a few minutes' walk from Ca Granda metro station, the modern 4-star Novotel Milano Nord Ca Granda hotel is in an ideal location for business trips and conferences, but also as a base for sightseeing in the center of Milan. 
The lilac metro line connects the 4-star Novotel Milano Nord Ca' Granda hotel to the Milano Porta Garibaldi train station, the San Siro stadium and the Porta Nuova and Isola districts (with their impressive buildings such as the Bosco Verticale towers).


  2 minutes walking from the metro station Lotto (M1 red line or M5 violet line).

  Milan Linate airport, 12 km from Novotel, is the most closest airport to the city and can be easily reached by car, bus or train.

  Central Station 3 km, Garibaldi Station 4 km.

  On-site parking with a fee

Informazioni utili

Upon Arrival
At your arrival you will find our Staff at the Welcome Desk to greet and make you feel welcome and as comfortable as possible, providing direction and all information about the meeting, seating, refreshments.

Refreshments
Coffee breaks and networking lunch will provide a pleasant moment of refreshment and an opportunity for you to network with your industry peers. Special care about the food quality, in particular to your dietary needs or preferences, from menus of local products and flavors to vegetarian dishes.



Conference Room
All our conference facilities are safe, healthy, comfortable, aesthetically-pleasing, and accessible. They are able to accommodate the specific space and equipment needs of the conference. Equipped for audio/visual, Free Wi-Fi to allow everyone to connect with just one click.



Informative literature
All the necessary information for the Conference is provided. The environment is important to us and that's why we try to make this meeting an experience of environmental sustainability.

Fee includes
Seat at the conference, copy of presentations of Speakers who allow the distribution, informative literature for the day, networking lunch, coffee break, organisational office assistance, certificate of attendance. 

Numeri utili

Ilaria Butta
Ilaria Butta Events & Training Executive
Enrico Pedroni
Enrico Pedroni Managing Director
Valeria Quintily
Valeria Quintily Project & Scientific Manager

Eventi passati

Prezzo della conferenza

1345.00 €

Super Early Bird

lunedì 6 luglio 2020

1090.00 €

Pagamenti accettati

  • Bonifico bancario
  • Carta di credito
  • PayPal

Per informazioni:

Contatti:

Ilaria Butta
Ilaria Butta Events & Training Executive
Enrico Pedroni
Enrico Pedroni Managing Director
Valeria Quintily
Valeria Quintily Project & Scientific Manager
Organizzata da

Formazione tecnico scientifica
in ambito farmaceutico
Via Roma 20 – 24022 – Alzano Lombardo (BG)
Tel: +39 035 515684

I Feedbacks dei partecipanti

Very focused and "hot topics" of RWE generation

Interesting topics. Speakers very well prepared and with interesting talks

Do this again! Superb agenda!

Nice combinations of theory and practical issues 

Deep insight of speakers during round table, nice discussion topics. Broad view with presentations/speakers, multiple relevant topics

Enough time for networking and discussion. Very well organized

Broad coverage of topic matter & subject matter experts from various countries backgrounds. Objective of conference achieved.

Mix of industry and academia/public. Good practical examples, illustrations to mark the point

Different point of view from HTA agency, interesting examples, NICE, to market access

Very interactive, focus, practical and very relevant

Perfect timing and location

Great presenters, lot of topics covered

Very good speakers!

I found EPI Forum latest conference very focus and targeted, yet still with the right amount of generalities that should better help appreciate the lessons that could be learned from these case examples. The size (not too big!) was also very conducive to interactions and thus some kind of brainstorming sessions.

Congratulations for the great organisation of the event and the high level of the speakers. I really enjoyed the meeting!

I numeri di LS Academy

2000
Anno di fondazione
1
Corsi organizzati
1
Conferenze organizzate
1
Professionisti formati

Tariffa Gruppi

Contattaci per partecipazioni multiple e beneficiare del migliore sconto

Pagamento sicuro con

Servizio clienti

Lunedì - Venerdì: 9:00 | 13:00 e 14:00 | 18:00
+39.035.515684 - info@lsacademy.com

Chiudi il menu
×
×

Carrello

European Epidemiological Forum

information request

European Epidemiological Forum

richiesta informazioni

European Epidemiological Forum

richiesta di sponsorizzazione

Termini e Condizioni

Corsi
la quota comprende: Ingresso al corso, documentazione didattica, pranzi e coffee break, assistenza segreteria organizzativa, attestato di partecipazione.
Lo sconto early bird non si applica alla quota per Freelance – Accademia – Pubblica Amministrazione.
Il corso si svolgerà al raggiungimento di un minimo di 8 partecipanti. In caso contrario verrà data comunicazione agli iscritti almeno una settimana prima dalla data del corso.
Per maggiori informazioni riguardanti l’iscrizione all’evento, potete contattare la segreteria organizzativa:
training@LSAcademy.com oppure tel. +39.035.515684


Conferenze

la quota comprende: ingresso alla conferenza, copia delle presentazioni dei relatori che le hanno rese disponibili, materiale informativo della giornata, networking lunch, coffee break, assistenza segreteria organizzativa, attestato di partecipazione. Per maggiori informazioni riguardanti l’iscrizione all’evento, potete contattare la segreteria organizzativa: events@LSAcademy.com oppure tel. +39(0)35.4123594

 

Webinars
la quota comprende: Ingresso al corso, documentazione didattica, assistenza segreteria organizzativa, attestato di partecipazione. Lo sconto early bird non si applica alla quota per Freelance – Accademia – Pubblica Amministrazione.  Per maggiori informazioni riguardanti l’iscrizione all’evento, potete contattare la segreteria organizzativa:
training@LSAcademy.com oppure tel. +39.035.515684


Condizioni comuni per Corsi e Conferenze

Termini di pagamento

L’importo dovrà essere versato ad EasyB S.r.l. all’atto dell’iscrizione tramite pagamento online (con carta di credito) o tramite bonifico bancario. In caso di bonifico bancario, l’importo dovrà essere versato a EasyB s.r.l. all’atto dell’iscrizione a:

EasyB S.r.l.
Via Roma, 20 – 24022 Alzano Lombardo (BG)
VAT: IT03633040161
Coordinate Bancarie:
BANCO BPM – Filiale di Carobbio Degli Angeli
SWIFT Code: BAPPIT21AY5
IBAN: IT81 F 05034 53960 000000003450

Solo la conferma dell’avvenuto pagamento consente la partecipazione all’evento. Seguirà fattura quietanzata. Iscrizioni ricevute in ritardo od oltre il numero massimo dei partecipanti o di figure professionali non in linea con il target dell’evento, potranno non essere accettate. Il pagamento della quota di iscrizione è dovuto contestualmente al ricevimento della scheda di registrazione. L’ammissione all’evento è confermata unicamente al ricevimento del pagamento. Potranno non essere accettate le iscrizioni ricevute in ritardo oppure oltre il numero massimo consentito dei partecipanti oppure di figure professionali non in linea con il target dell’evento.

Cancellazione
L’eventuale disdetta di partecipazione dovrà essere comunicata in forma scritta ad EasyB entro una settimana dall’evento. Il rimborso è pari al 70% della quota. Cambiamenti nei nominativi dei partecipanti: da comunicare ad EasyB entro 7 giorni dalla data dell’evento. EasyB si riserva il diritto di posticipare o cancellare un evento, di cambiare la location di un evento o di modificare il panel dei relatori di un evento, di modificarne l’esecuzione da residenziale a webinar. EasyB non è responsabile per qualsiasi perdita o danno risultante da sostituzione, cambiamento, rinvio o cancellazione di un evento per cause al di fuori del proprio controllo, incluso a titolo esemplificativo e non esaustivo, cause di forza maggiore, disastri naturali, sabotaggi, infortuni, vertenze sindacali, atti di terrorismo, guerre, epidemie, pandemie, e/o blocchi dell’autorità ( c.d. factum principis).

Informativa Privacy
Ai sensi dell’art. 13 Reg. UE 27 Aprile 2016 n. 679, La informiamo che EasyB S.r.l., corrente in Alzano Lombardo (BG), via Roma 20 C.F e P.Iva 03633040161, in qualità di titolare del trattamento, tratterà i dati personali da lei volontariamente forniti solo previo consenso e nel rispetto dei principi dettati dal Regolamento Europeo in materia di protezione dei dati personali per l’invio di newsletter, per finalità di marketing (invio materiale pubblicitario, ricerche di mercato e comunicazione commerciale) e comunicazione dei medesimi dati a terzi (docenti e relatori, board scientifico, aziende che sponsorizzano la conferenza) anche per finalità di marketing. Potrà leggere l’informativa completa, compresi i diritti a lei spettanti e le modalità per l’esercizio degli stessi, cliccando su questo link.