- OUR CORPORATE FRIENDS -
Meet our friends who are doing their bit to support our #RareRevolution
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- EVENTS -
March 30th – April 3rd
FREE TO ATTEND: Covid-19 has created one of the most challenging environments in decades. Ironically, despite the travel restrictions, it’s more important than ever for the pharma industry to share ideas and inspiration. We have therefore decided not to cancel, but to reinvent eyeforpharma Barcelona 2020 as a virtual event, FREE of charge for all to engage with. Between March 30th and April 3rd, more than 5000+ attendees will be able to experience the first online edition of this event. You can expect 100+ confirmed speakers, including patient advocates and panels, 70+ confirmed sessions, full audience interactivity with all presentations, fireside chats and panels, a virtual exhibition and a one-to-one meeting service.
Our ambition is to ensure we don’t become isolated in our isolation.
Click here to see the complete agenda.
Click here to see the complete agenda.
Be a part of the rare disease patient and family gathering of the year!
The 2020 Living Rare, Living Stronger™ NORD Patient and Family Forum (Cleveland, Ohio; May 14-16) is a three-day conference filled with fun, learning and connecting.
The agenda includes sessions in which patients and their families can gain insight and practical tools for living their best lives with rare diseases, with four tracks provided for newly diagnosed patients, long-term patients, caregivers, physicians and medical students. Attendees can customize their experience by choosing one track to follow or by building their own schedule to best fit their interests.
Registration includes a ticket to a very special event—the 2020 Rare Impact Awards®—honouring those who are making extraordinary contributions to the lives of rare disease patients and caregivers. The awards ceremony will take place at the iconic Rock and Roll Hall of Fame. This will be a show you won't want to miss!
The agenda includes sessions in which patients and their families can gain insight and practical tools for living their best lives with rare diseases, with four tracks provided for newly diagnosed patients, long-term patients, caregivers, physicians and medical students. Attendees can customize their experience by choosing one track to follow or by building their own schedule to best fit their interests.
Registration includes a ticket to a very special event—the 2020 Rare Impact Awards®—honouring those who are making extraordinary contributions to the lives of rare disease patients and caregivers. The awards ceremony will take place at the iconic Rock and Roll Hall of Fame. This will be a show you won't want to miss!
To view the agenda, learn more or register, visit:
https://rarediseases.org/living-rare-forum/?referral=rare_revolution
https://rarediseases.org/living-rare-forum/?referral=rare_revolution
EYEFORPHAMA PHILADELPHIA 2020 April 15th to 16th
eyeforpharma USA 2020 (Philadelphia, April 15-16) is North America’s largest commercial conference, bringing together 1000+ senior-level industry leaders, spanning commercial, marketing, digital, medical, patient engagement, RWE, access and clinical trials functions. eyeforpharma Philadelphia provides 2 days of cutting-edge case studies, top exec-led panels, intimate roundtables, workshops and lunch and learns, for the best learning and networking opportunities in the US pharma events calendar.
The European Conference on Rare Diseases & Orphan Products (ECRD) is recognised globally as the largest, patient-led rare disease event.
People living with a rare disease have the right to reach their highest potential of well-being; join us in ECRD 2020 Stockholm to take part in discussions to inform and build the future ecosystem for rare disease policies and services.
Leading, inspiring and engaging all stakeholders to take action, ECRD is where innovative solutions in the rare disease field are born. The Conference is an unrivalled opportunity to network and exchange invaluable knowledge with all stakeholders in the rare disease community from over 50 countries around the world - patient representatives, policy makers, researchers, clinicians, industry representatives, payers and regulators.
Be part of the global rare disease community at ECRD 2020 Stockholm and shape the future for people living with a rare disease!
People living with a rare disease have the right to reach their highest potential of well-being; join us in ECRD 2020 Stockholm to take part in discussions to inform and build the future ecosystem for rare disease policies and services.
Leading, inspiring and engaging all stakeholders to take action, ECRD is where innovative solutions in the rare disease field are born. The Conference is an unrivalled opportunity to network and exchange invaluable knowledge with all stakeholders in the rare disease community from over 50 countries around the world - patient representatives, policy makers, researchers, clinicians, industry representatives, payers and regulators.
Be part of the global rare disease community at ECRD 2020 Stockholm and shape the future for people living with a rare disease!
Register here https://www.rare-diseases.eu/