Maximising engagement with healthcare professionals
14th December 2021 @ 11:00 am - 12:30 pm
Free
Join this webinar to explore the practical things patient groups can do to make sure they are engaging with HCPs in the most beneficial way.
Most rare diseases are not concentrated in one area or country and do not affect one singular body system, which makes finding healthcare professionals (HCPs) or specialists who understand them a real challenge for patients and patient organisations. Yet, it is often a top strategic priority for patient organisations to find and engage with these professionals to drive faster diagnoses, better understanding of and research into rare conditions.
This can be a real challenge when most HCPs have a very limited knowledge of rare conditions. HCPs often look straight to google for their research where they can be met with misinformation and do not always find the patient organisations that are the real experts straight away. Thus, it falls onto the shoulders of these patient organisations to make themselves more visible and receptive to engagement with healthcare professionals. Whether at a basic operational level, an organisational level, through external collaborations or even by working with the organisations such as the NHS and NICE.
This webinar will:
Explore the different levels on which patient organisations can base their engagement with medical professionals
Cover the practical things patients can do (no matter what size or capacity) to engage efficiently and sustainably with HCPs
Highlight case studies from across the rare space of what different patient groups are doing
Please note: This is the first in a series of two webinars which will explore engagement with HCPs.
This website uses cookies to improve your experience. We'll assume you're ok with this, but you can opt-out if you wish. Cookie settingsACCEPT
Privacy & Cookies Policy
Privacy Overview
This website uses cookies to improve your experience while you navigate through the website. Out of these cookies, the cookies that are categorized as necessary are stored on your browser as they are as essential for the working of basic functionalities of the website. We also use third-party cookies that help us analyze and understand how you use this website. These cookies will be stored in your browser only with your consent. You also have the option to opt-out of these cookies. But opting out of some of these cookies may have an effect on your browsing experience.
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.
Join this webinar to explore the practical things patient groups can do to make sure they are engaging with HCPs in the most beneficial way.
Most rare diseases are not concentrated in one area or country and do not affect one singular body system, which makes finding healthcare professionals (HCPs) or specialists who understand them a real challenge for patients and patient organisations. Yet, it is often a top strategic priority for patient organisations to find and engage with these professionals to drive faster diagnoses, better understanding of and research into rare conditions.
This can be a real challenge when most HCPs have a very limited knowledge of rare conditions. HCPs often look straight to google for their research where they can be met with misinformation and do not always find the patient organisations that are the real experts straight away. Thus, it falls onto the shoulders of these patient organisations to make themselves more visible and receptive to engagement with healthcare professionals. Whether at a basic operational level, an organisational level, through external collaborations or even by working with the organisations such as the NHS and NICE.
This webinar will:
Please note: This is the first in a series of two webinars which will explore engagement with HCPs.
Details
Organisers