Patient advocacy icon

Patient advocacy

Core data points

At a glance

39 patient groups shared a commentary
49% Regularly or sometimes engage with drug regulators
74 Comments / feedback
5 Sub-types of patient advocacy represented
21 Countries represented
~815.4K Approximate number of patients reached by these groups

Survey insights

Forty-nine per cent of patient advocacy groups represent patient interests to regulators. Participation in HTA and reimbursement reviews is most common (23%), while fair medicine pricing is the leading advocacy priority (21%).

Patient groups representing each Patient advocacy sub-type

91 patient groups across 5 sub-types

  • Health activist 30
  • Patient advocacy 20
  • Patient rights 19
  • Drugs and related treatments 5
  • Training 4

Patient group voices

Patient group goals

The percentages below highlight how the 39 patient groups interact with regulators and advocate for patient interests. As respondents may be represented in more than one area, percentages may not total 100%.

interactions

How patient groups interact with drug regulators

Find out what the goals mean
23 mentions
8 mentions
5 mentions
5 mentions
2 mentions
actions & advocacy

How patient groups get access to medicines

Find out what the goals mean
12 mentions
9 mentions
4 mentions
2 mentions
1 mention
1 mention

GET THE REPORT

Access the full findings

Our research covers 2,262 patient groups representing 100 countries and 45 therapy areas. The sample report shows you the depth of analysis for a single country or therapy area. To access any other reports, please get in touch.

Visit patient-view.com to gather more information or email: Alex Wyke, alexwyke@patient-view.com