Beacon is delighted to announce its next online workshop: Understanding access and reimbursement
Getting wider access to drugs for as many patients a possible is a clear priority in the drug development process, especially for patient groups who are working to secure research into and treatments for their rare conditions. However, understanding how to secure access to newly developed treatments is an often-neglected challenge. The processes involved in securing reimbursement can be intimidating to patient groups and act as a real barrier to engagement.
This workshop will outline the basics of access and reimbursement: what it means, when it happens, and who is involved. It will also explore the key ways in which patient groups can contribute to the process and what should they be prepared for. Attendees will leave feeling more confident in what the access and reimbursement process involves and where they can add value.
Day one of our workshop will explore the basics of what access and reimbursement is and what this means practically for patients in the UK.
The session will answer the following questions:
The session will also feature a presentation from speakers at the MHRA, as they outline their new Innovative Licensing and Access Pathway (ILAP) and what it means for patient involvement in access to health technologies.
In the UK, for most patients to receive a treatment, it needs to be available from the NHS. This only happens if it is reimbursed – a decision taken in England by an organisation called NICE (National Institute for Health and Care Excellence). To make these decisions NICE use a process called a health technology appraisal (HTA). This is designed to assess the benefits of the treatment to patient’s health and quality of life versus the cost to the country of providing that treatment. Medicines with a high value for their cost will be reimbursed. The HTA process is long and can seem complicated to those unfamiliar with the way it works, the people involved, and the language used. However, it is essential for patients to understand this process, as they have a vital role to play in it by helping to provide evidence that is able to demonstrate the value of the new treatment to their population. In this way patient groups can ensure the best outcomes for their patient community.
The session will include speakers from NICE and will cover:
There is room for patient and patient group involvement throughout the journey to access and reimbursement and it can make a real difference to the outcome of the process. There are ideal ways that patient groups can engage and frameworks that can be utilised to ensure the best results for patients.
The session will focus on:
Session recordings will only be available to those who attended the event or provide reasonable notice that they cannot attend. Recordings will not be made publicly available.