Agenda van de ACRON

De ACRON is de branchevereniging van CRO’s in Nederland. Wij behartigen de collectieve belangen van de aangesloten bedrijven (leden). Dit doen we door middel van het organiseren van bijeenkomsten, zowel besloten als open, netwerk en lobby activiteiten met als voornaamste doel om Nederland als onderzoeksland optimaal te laten functioneren. Bekijk hieronder de agenda van evenementen van de ACRON en Contract Research Organisaties (CRO’s) in Nederland:

Evenement details:

  • di
    25
    feb
    2020

    The Patient Centricity Effect – How it benefits Patients, Sites and Sponsors

    10.00 - 11:30 uurEUCROF Online event

    Attendance Fee:
    € 90,- for non-EUCROF members
    € 60,- for EUCROF members

    Overview

    Patient centricity has become something of a buzz phrase over the last few years. However, behind the name, a concept that offers real value can be found. Such benefits will be discussed during this webinar, 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 provide you with data and examples you can bring back to your own organization, in order to support the development and growth of patient centric practices. Furthermore, a collaborative discussion about the future of patient centricity and its effects 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 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 his/her parents, even when such an 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.

    Presenters:

    Rosamund Round
    Vice President, Patient Innovation Center
    Parexel International

    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)

    See full biographies on our website

     

    Registration

    >> How to register?
    1) Go to our Eventbrite page
    2) Click on the green "REGISTER" button
    3) Check your order and click on the green "CHECKOUT" button
    4) Fill in all the necessary information and validate your order

    >> Confirmation
    You will receive 2 confirmation emails :
    A) One from Eventbrite with your invoice
    B) One from Assia Rosati, sent by GoToWebinar, our webinar platform, with all the necessary information to connect on the D-Day!

Contact

Heb je vragen over ACRON? Neem eenvoudig contact met ons op.