25 February 2020 - The Patient Centricity Effect – How it benefits Patients, Sites and Sponsors – Practical cases from paediatric studies

Webinar Topic

The Patient Centricity Effect – How it benefits Patients, Sites and Sponsors – Practical cases from paediatric studies

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Webinar Date & Time

25 February 2020 from 10:00 AM to 11:30 AM (CEST)


Webinar Overview

Patient centricity has become something of a buzz phrase over the last few years. However, behind the name lies a concept that offers real value. During this webinar, these benefits will be discussed, highlighting:

  1. Results from recent research that quantifies the positive business impact to sponsors by taking a patient centric approach 
  2. Exploration of real examples where the patient has benefited from being put at the heart of clinical research
  3. Advantages experienced by sites when patients are central to study planning and implementation


This informative session will arm you with data and examples to take to your own organization to support the build and growth of patient centric practices. In addition, a collaborative discussion about the future of patient centricity and its effect on the industry will complete the webinar.


Moreover, the webinar will provide practical examples on how to involve children in clinical trials. 
A child-friendly approach is necessary not only in the daily clinical practice, but throughout the research and development process, from setting research priorities, involvement in research design and planning, research conduct through to dissemination and communicating research findings. In case of studies involving children, age-tailored information booklets, assent forms and summaries of the results should be written in age appropriate, simple and understandable language to ensure ease reading by parents and children. Moreover, the investigators should obtain agreement from the child in addition to informed consent of the parents, even when this agreement is not mandatory by law. 
An innovative approach for the patients’ involvement in paediatric clinical research is represented by the Young Persons Advisory Groups, an organization composed of youths, patients and carers actively participating in clinical research and advising researchers and their teams.


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Presenters

Rosamund Round
Vice President, Patient Innovation Center
Parexel International


Rosamund is the head of Parexel’s Patient Innovation Center, spending her time devoted to improving patient access to and experiences in clinical research. Focused on the reduction of geographical, financial and practical barriers to study participation, Rosamund is excited by the industry shift towards a truly patient centric approach. An early role in an oncology clinic at Massachusetts General Hospital (USA), sparked her passion for putting patients at the centre of clinical research planning and implementation. Since then, she has created numerous tools and services that better meet the information and practical needs of clinical trial participants. She is delighted to share her learnings around patient centricity and innovation in patient engagement.



Mariangela Lupo

Patients Advocacy Manager
TEDDY European Network of Excellence for Paediatric Clinical Research
Head of the Training and Advocacy Area
Consorzio per Valutazioni Biologiche e Farmacologiche (CVBF)

 

Patients Advocacy Manager at TEDDY European Network of Excellence for Paediatric Clinical Research. Head of the Training and Advocacy Area at Consorzio per Valutazioni Biologiche e Farmacologiche (CVBF) and Team Leader of KIDS Bari, the first YPAG in Italy.
Within the TEDDY Network she is responsible for the development and organization of educational materials and activities for paediatric patients in the EJPRD (European Joint Programme for Rare Diseases); Networking Manager of H2020 ID-EPTRI (European Paediatric Translational Research Infrastructure); member of the Public Patients Involvement (PPI) team in c4c (conect4children) project.
Member of Working Parties of Enpr-EMA at EMA (Young Patients Advisory Groups; Training) and member of the Working Groups Communication and Events & Training at EUCROF. 

 

 

 

 

 

Attendance Fee

€ 90,- for non-EUCROF members

€ 60,- for EUCROF members

 

Deadline for registration

24 February 2020

 

How to register?

1) Go on the REGISTRATION PAGE and click on the green "REGISTER" button

2) Check your order and click on the green "CHECKOUT" button

3) Fill in all the necessary information and validate your order

 

Confirmation

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