Data

2 - 3 March 2020

Location

Berlin

Lingua

English

Patient Partnering in Clinical Development

Iscriviti
Patient Partnering in Clinical Development

How to Best Integrate Patients into your Strategies and Operations in Clinical Development – Step III


Important milestones are reached for patient-oriented trials!

The third Patient Partnering in Clinical Development (PPCD) conference will present and discuss approaches with patients, their advocates, study nurses, physicians, industry partners and all stakeholders involved on 2-3 March 2020 at Berlin.

Strong awareness about the need of patient engagement was built up in the last decade. Now we have the first implementation of regulations at the FDA, the European Medicines Agency and the National Institute for Health and Care Excellence. We have to learn to execute clinical research at its best with patients in mind in the first place. We have new roles in pharma and the CRO industry who help to put in place the requirements to streamline and optimize all the efforts around the trials.

Important changes are linked to the voice of patients who become experts of their disease and to the digital technologies that needs to be created around the patients and physicians.

The new trials very often include hand-held data capture where applicable, home nursing and logistic support keeping in mind that in some diseases and pediatric indications very often the whole family is involved in the successful participation in the trial.

Therefore, the motto of the future is “Bring the trial to the patient instead of making the patient come to the trial”.

The 2020 edition of PPCD is offering a training workshop on blockchain applications in clinical research as part of the agenda to see how it is improving transparency, traceability and quality.

Speaker presentations, panel discussions and the interactive workshop will share thoughts on:

  • Blockchain applications
  • Early phase development
  • Clinical development and operations
  • Regulatory aspects


Scientific board

Raphaela Schnurbus - Clinical Research Solutions Management and Business Development Director at Premier Research
Doris Christiane Schmitt - Consultant for patient communication and Member of the leading team EUPATI, Germany
Nancy Meyerson-Hess - Expert Advisor admedicum Business for Patients and Chief Compliance and Regulatory Officer eMQT


Who should attend?

The conference is addressed to all Professionals working around the clinical trial from early onset up to late stage development and market authorization: Pharmaceutical and Biotechnology companies, Clinical Research Organizations, Academic Centres, Hospital Centres, Patient Associations and Clinical Technology companies with a strong interest in integrating patient experts into their strategies and operations in healthcare development.


Pegasus Networking Reception

LS Academy and admedicum Business for Patients are pleased to invite you to the Pegasus Networking Reception on Monday 2 March from 18.00 - 20.00.


Sponsor

Patronage

Brochure and Certificate

Download programme
Certificate of attendance

2 Marzo 2020

The interactive workshop will focus on:

  • Use of blockchain in transforming healthcare
  • What you need to consider in setting up blockchain for pharmaceutical and healthcare use case
  • A demo on Patient Data Use case and exploring example use cases from attendees

Aji Barot Aji Barot – VP at Pharma (EMEA)
Adama Ibrahim Adama Ibrahim – Associate Director, Global Clinical Operations at Biogen

Coffee breaks and networking lunch will provide a pleasant moment of refreshment and an opportunity for you to network informally with your industry peers. Quality food, with particular attention to your dietary needs.

The interactive workshop will focus on:

  • Use of blockchain in transforming healthcare
  • What you need to consider in setting up blockchain for pharmaceutical and healthcare use case
  • A demo on Patient Data Use case and exploring example use cases from attendees

Aji Barot Aji Barot – VP at Pharma (EMEA)
Adama Ibrahim Adama Ibrahim – Associate Director, Global Clinical Operations at Biogen

The National Institute for Health and Care Excellence (NICE) was established in 1999, and now has a reputation as an international leader in evidence synthesis, guideline development and technology evaluation. We will build and enhance this reputation with an new offer that integrates our advice along care pathways, accessible to users whenever and wherever they need it, which is always up to date. To achieve this, we will make effective use of digital technologies and artificial intelligence, with the aim of improving care and facilitating the use of new, cost effective technologies. Traditionally our recommendations have been based on the best available research evidence, supported by an economic analysis. Over the past 20 years, however, the availability of data – alongside research studies – has rapidly increased. Now some of our work is based on an analysis of real world data, such as for selected new cancer drugs. To build on this work, we have set up a new programme to routinely inform our guidance with analyses of relevant data. This will be particularly useful for answering questions where there is no published research, and to determine the effect of new interventions in day to day practice.

Adrian Jonas Adrian Jonas – Associate Director for Data and Analytics at NICE

Patients are experts in their own experience of their condition and in the effect of using a medical product. Therefore, they should be meaningfully involved throughout the medical product development process, and their views and experiences should be taken into consideration by regulators.

Both in the United States (US) and in the European Union (EU), the authorities are focused on getting better patient experience data included in applications submitted for their assessment and decision-making regarding new medicines and/or the extended clinical use of approved medicines.

The US Food and Drug Administration (FDA) recently set up a guidance framework for gathering patient experience data in a systematic and evidence-based manner, as mandated by the 21st Century Cure Act Law from 2016.

This session will provide a brief update on current and future plans that applicants need to be aware of in relation to the US as proposed by the FDA, and in the EU by the European Commission (EC)/European Medicines Agency (EMA).

Participants will be taken through the process and systems to capture patient experience data in clinical trials. Examples will be presented illustrating how patient experience data can add value throughout the drug development process and may be included in a label claim.

Jens Harald Kongsoe Jens Harald Kongsoe – Founder, CEO at Clinical Survey Outcomes

Patient Engagement in Global Alliance (PEGA-SUS) networking events gather interested patients and patient organizations with industry (pharma, biotech, medtech) and any other potentially interested stakeholders within healthcare around the subject of patient engagement in an informal way. Pegasus events happened in Berlin, Cologne, Barcelona, and Leiden in 2019 and brought together over 120 people.

This event will feature an interactive parliamentary-style debate moderated by Paola Kruger, EUPATI Italy, and Roger Legtenberg, Upstrong, former CEO of PSR Clinical Research, where participants will be guided through a lively debate of current issues in patient engagement in research and development.

This is the first Pegasus event of 2020 and is taking place alongside the larger Patient Partnering in Clinical Development conference and both attendees of that conference and local stakeholders interested in patient engagement will join us for the evening. admedicum Business for Patients is the initiator and administering entity and joins with other interested patient organizations and companies to create the events. PEGASUS events are not for marketing or commercial purposes. Events are a platform for networking between industry and patients and knowledge exchange.

3 Marzo 2020

In the search for new medicines and improved treatment methods there is an ever-increasing pressure to enhance both effectiveness and efficiency of the drug and the drug development process. In order to meet these expectations it is of vital importance that stakeholders/participants are much more aligned and work closely together, that administrative hurdles are reduced and that patients, being the end-users, are consulted and included throughout the different stages of the development chain, from discovery until market introduction of the drug. It is claimed that active patient participation in the various stages of new medicines development projects will increase the (average) success rate of projects and will enhance the level of acceptance of a drug upon introduction in the market.

Having said this, it is not an easy task for the professionals who are active in the chain to realise these desired improvements. In addition, investigators and project managers are often struggling with the concept of patient involvement in their projects and how to ‘operationalise’ this. This holds true for both the earlier (pre-clinical and clinical) stages but and even more for the later (peri- and post-clinical) stages of the development process. In order to be fully convinced, some doctors and investigators feel the need to have the concept of active patient participation supported by some scientifically sound evidence that it does really add value to include this in their new way of working.

A more in-depth evaluation of the matter adds further complexity, as it reveals not just the above issue, but also numerous other roadblocks that need to be recognised, addressed and removed on the road to a successful implementation of full patient involvement.

In this lecture, some considerations, new insights and promising developments around patient involvement and participation (why/what/how) will be shared. The earlier mentioned roadblocks will be discussed, and suggestions will be given on how to overcome or remove them. Furthermore, a few successful examples will be given of approaches that enhance collaboration and active patient involvement in The Netherlands. These best practices will be used to postulate some of key success factors that contribute to realising a successful drug development chain.

Eric Roos Eric Roos – Board member Dutch Clinical Research Foundation (DCRF); Chairman Dutch Parkinson Patient Association (Parkinson Vereniging, PV)

Seeking feedback from patients on informed consent and support from patient organisations in patient recruitment initiatives is frequent practice by pharma companies and CROs. However, patients can and should be involved in many more processes of the new treatment development process to ensure that the new treatments are meaningful to their needs. Why is it not happening to a much larger degree? There is a multitude of reasons for the different stakeholders involved in the process reaching, e.g., from lack of interest or willingness for collaboration in patient organisations to obstacles in company/CRO structures and processes on involving patients to not being able to find each other and lack of clarity on the rules for collaboration. This presentation will provide an overview over recent developments in educating and engaging patients in different steps of the new treatment development and access to treatment processes as well as guidance on ground rules and governance infrastructure for collaboration.

Ingrid Klingmann Ingrid Klingmann – Chairman at European Forum for Good Clinical Practice (EFGCP)

Moderator: Philipp Gallwitz - Founding Partner of admedicum Business for Patients

Jordi Cruz Villaba Jordi Cruz Villaba – President of Rare Disease in Catalonia and member of the board of Rare Disease Federation, Spain
Paola Kruger Paola Kruger – Patient Expert
Mitchell Silva Mitchell Silva – CEO at Esperity

Coffee breaks and networking lunch will provide a pleasant moment of refreshment and an opportunity for you to network informally with your industry peers. Quality food, with particular attention to your dietary needs.

The role of patients is more important than ever, and an empowered patient likes to engage more with its health and has rising needs for trusted information. They are taking greater control of the treatment of their disease. Getting used to modern technologies patients’ expectations on good communication are rising and easy access to reliable and understandable information becomes a must. Providing product information electronically is a first step towards better communication.

The session will talk about the benefits of changing from static product information into its electronic form, it will touch upon the current discussion on European level and highlight some ongoing initiatives.

Rüdiger Faust Rüdiger Faust – Head Telematics & Digital Solutions at Grünenthal GmbH

The role of Patient Advocacy Organizations (PAOs) has been evolving over the past few decades and the impact that PAOs can have in the planning, design and execution of clinical research trials has been expanding. It is not unusual for PAOs or even individual patients and/or their care network members to be involved in the identification or refinement of disease-specific endpoints, to offer insights on protocol design or to offer advice on enrollment or retention obstacles and how to overcome them. Indeed, the industry has come to realize the benefits of engaging with patients and their care partners at almost every step of the clinical development process.

In this presentation we will explore how a CRO’s engagement with a specific PAO impacted the country and site mix in a rare disease trial, resulting in a complete change in site selection strategy. This engagement resulted in the first ever trial in this indication being placed in this specific country, all as a result of the efforts of the PAO and the CRO to dig deeper and work together to understand the treatment landscape in that country.

Juliet Moritz Juliet Moritz – Vice President, Patient and Stakeholder Engagement at Premier Research

Coffee breaks and networking lunch will provide a pleasant moment of refreshment and an opportunity for you to network informally with your industry peers. Quality food, with particular attention to your dietary needs.

Engaging patients in clinical research decisions and activities seems a logic step when developing new drugs for patients. However, engaging patients is still not happening in all clinical trials as much as it could be done. This presentation will give an insight into Pfizer’s journey identifying challenges and opportunities involving patients in clinical research. A cross functional team has enabled study teams to effectively use patient insights to optimize protocol development and study conduct. Some examples of patient engagement and outcomes will be included in the presentation.

Christina Claussen Christina Claussen – Director Patient Relations & Alliance Management at Pfizer Pharma GmBH
Stefan Mikus Stefan Mikus – Signal Interpretation Lead, Director at Pfizer Pharma GmBH

Patients say they want trusted relationships with clinical research staff based on clear, transparent communications. Yet too often patents are left feeling like they are not a valued partners in the research process. In response, Janssen developed HealthCaring Conversations for Clinical Research™, an initiative to help improve the trial experience for both patients and professionals. Based on an evidence-based communications framework, Health Caring Conversations:

  • provides a universal platform for sites to forge deeper connections with all patients in all phases of the clinical trial journey
  • ensures a consistent structure for sites to understand and address individual patient needs
  • facilitates empowering patients via consistent, structured, and personalized conversations

Caroline Bracke Caroline Bracke – Program Manager, Investigator & Patient Engagement at Janssen Research & Development

There is no question about the value of patient involvement in clinical research. Depending on development phase and type of input needed, patients with specific expertise and knowledge, at least with a basic understanding of the development process for medicinal products, with own experiences as patient/parent (in case of pediatric development) in the condition to be discussed and/or foundation in patient advocacy or patient advisory groups are sought. The EUPATI competency model, for example, provides a good basis for selecting patients. Even though clinical development proceeds on a global level, standard of care varies across countries. In Germany, involvement is increasingly desired by national patient representatives. Concurrently, existing relationships between local patient relations experts of pharma companies with national patient/parent representatives and patient advisory groups can simplify interaction and attract participation, strengthen the relationship and yield additional activities for treatment-accompanying health care optimization. Using the example of a multinational patient involvement project, the two speakers will discuss how, in addition to personal competencies, choosing the right geographical representation can be relevant and value enhancing.

Heidrun Hildebrand Heidrun Hildebrand – Global Program Head at Bayer AG
Jens Lipinski Jens Lipinski – Patient Relations at Bayer Vital GmbH

Coffee breaks and networking lunch will provide a pleasant moment of refreshment and an opportunity for you to network informally with your industry peers. Quality food, with particular attention to your dietary needs.

Presentation on the feasibility and benefits of creating a vendor/pharma independent, open source, Blockchain network to keep the real identity of the patients protected while allowing the possibility to:

  • Inform patients on the outcome of the research they participated in and inform them on how their data is supporting novel medical research;
  • Seek additional patient consent;
  • Seek additional information from patients on treatment outcome;
  • Empower the patients to choose which of their data can be used for what medical research;
  • Link different anonymized datasets for more powerful advanced analytics;
  • Link real world data with clinical trial data and diagnostics data;
  • Avoid dual enrollment in clinical trials.

In this very early phase of the PEPS project, the purpose of the presentation is to obtain early feedback from patient engagement specialists to build the project on strong foundation.

Benoit Marchal Benoit Marchal – Senior Project Manager at Roche

Patients need their health data.

Pharma need PRO and RWE for new clinical trials.

Hospitals need access to patients for continuity of care.

How can all these actors of the health of tomorrow work better together while respecting their roles and values?

Vincent Keunen, CEO and founder of Andaman7, but also successful entrepreneur and cancer survivor, proposes a new paradigm: by empowering patients with their health data, they can feel safer, be more engaged in their health and contribute to the needs of hospitals and the research sector (pharmaceutical companies, medical device manufacturers, CROs and academic actors). Vincent will explain how the combination of the mobile applications and the peer-to-peer HIP (Health Intermediation Platform) can solve all three problems. In a very effective way, that reduces costs, while strictly respecting users privacy and augmenting data security.

By attending this talk, you will learn how patients, hospitals and medical researchers can work better together to find new cures and treat patients better.

Vincent Keunen Vincent Keunen – Founder and CEO at Andaman7

Additional information available soon

Cesare Spadoni Cesare Spadoni – co-founder and Chief Operating Officer of Oncoheroes Biosciences Inc.

Coordinatori Scientifici

Nancy Meyerson-Hess
Nancy Meyerson-Hess Expert Advisor admedicum Business for Patients and Chief Compliance and Regulatory Officer eMQT
Doris Christiane Schmitt
Doris Christiane Schmitt Consultant for patient communication and Member of the leading team EUPATI, Germany
Raphaela Schnurbus
Raphaela Schnurbus Clinical Research Solutions Management and Business Development Director at Premier Research

Relatori

Aji Barot
Aji Barot VP at Pharma (EMEA)
Caroline Bracke
Caroline Bracke Program Manager, Investigator & Patient Engagement at Janssen Research & Development
Christina Claussen
Christina Claussen Director Patient Relations & Alliance Management at Pfizer Pharma GmBH
Jordi Cruz Villaba
Jordi Cruz Villaba President of Rare Disease in Catalonia and member of the board of Rare Disease Federation, Spain
Rüdiger Faust
Rüdiger Faust Head Telematics & Digital Solutions at Grünenthal GmbH
Heidrun Hildebrand
Heidrun Hildebrand Global Program Head at Bayer AG
Adama Ibrahim
Adama Ibrahim Associate Director, Global Clinical Operations at Biogen
Adrian Jonas
Adrian Jonas Associate Director for Data and Analytics at NICE
Vincent Keunen
Vincent Keunen Founder and CEO at Andaman7
Ingrid Klingmann
Ingrid Klingmann Chairman at European Forum for Good Clinical Practice (EFGCP)
Jens Harald Kongsoe
Jens Harald Kongsoe Founder, CEO at Clinical Survey Outcomes
Paola Kruger
Paola Kruger Patient Expert
Jens Lipinski
Jens Lipinski Patient Relations at Bayer Vital GmbH
Benoit Marchal
Benoit Marchal Senior Project Manager at Roche
Stefan Mikus
Stefan Mikus Signal Interpretation Lead, Director at Pfizer Pharma GmBH
Juliet Moritz
Juliet Moritz Vice President, Patient and Stakeholder Engagement at Premier Research
Eric Roos
Eric Roos Board member Dutch Clinical Research Foundation (DCRF); Chairman Dutch Parkinson Patient Association (Parkinson Vereniging, PV)
Mitchell Silva
Mitchell Silva CEO at Esperity
Cesare Spadoni
Cesare Spadoni co-founder and Chief Operating Officer of Oncoheroes Biosciences Inc.

Coordinatori Scientifici

Nancy Meyerson-Hess
Nancy Meyerson-Hess Expert Advisor admedicum Business for Patients and Chief Compliance and Regulatory Officer eMQT
Doris Christiane Schmitt
Doris Christiane Schmitt Consultant for patient communication and Member of the leading team EUPATI, Germany
Raphaela Schnurbus
Raphaela Schnurbus Clinical Research Solutions Management and Business Development Director at Premier Research

Sponsors

Patrocini

Media Partners

Sede della Conferenza

Courtyard Berlin City Center
Axel Springer Strasse 55 - Berlin

Courtyard Berlin City Center is ideally located in the heart of downtown, in walking distance to many famous Berlin attractions such as Friedrichstrasse, Alexanderplatz, Brandenburg Gate, Checkpoint Charlie, Memorial of the Berlin Wall and Potsdamer Platz.

  Spittelmarkt Underground Station is just a 4-minutes walk from the hotel, providing connections to Alexanderplatz and Potsdamer Platz in just 10 minutes.

  Spittelmarkt (at 270 mt)

  Berlin-Schönefeld Airport SXF (21 Km), Berlin-Tegel Airport TXL (12 Km)

  Berlin Central Station, Hauptbahnhof (3,5 Km)

  In addition to the hotel venue, here is some recommended hotels for accommodation in the nearby:

            - Cosmo Hotel Berlin Mitte (at 280 mt)

            - Titanic Comfort Hotel Berlin Mitte (at 450 mt) 

            - Mercure Hotel & Residenz Berlin Checkpoint Charlie (at 500 mt)

  On-site parking with a fee

  La Banca Restaurant (1,1 Km), Cookies Cream (1,8 Km), Restaurant Maximilians Berlin (1 Km)

This hotel does not provide shuttle service.

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

Eventi passati

Prezzo della conferenza

Ordinary

1250.00 €

Pagamenti accettati

  • Bonifico bancario
  • Carta di credito
  • PayPal

Per informazioni:

Contatti:

Ilaria Butta
Ilaria Butta Events & Training Executive
Enrico Pedroni
Enrico Pedroni Managing Director
Organizzata da

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

I Feedbacks dei partecipanti

Networking; learned a lot about opportunities to involve patients in  various activities

Network, Sharing the knowledge

Small group, possibility to network and agenda is really patient engagement focused

Excellent presentations, excellent discussions, really great choice location. Congratulations organizers and scientific board

Only positive: very expert presenters in this field, very good discussion at high level

Speakers were excellent with very different backgrounds; break out sessions were thought provoking/engaging

Very well organized and good topics

Great agenda, very good speakers

Great networking and talks

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

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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


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. 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.

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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, 
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