Registrations Open

3rd International
Patient Summit

"From Rare to Common: Uniting Patient Voices for Better Health"
27–28 November 2026 New Delhi, India DakshamA & PAIR
Visit IPS Website Download Brochure
3rd
Edition
2
Day Summit
150+
Expected Delegates
50+
Expert Speakers
27–28 November 2026
New Delhi, India
Co-organised by DakshamA & PAIR
Asia-Pacific Focus

About the Summit

The International Patient Summit (IPS) is a premier platform where patients, caregivers, healthcare professionals, policymakers, and industry leaders converge to amplify patient voices and drive meaningful change in healthcare delivery across the Asia-Pacific region.

IPS was born out of the collective conviction that patient voices must be at the centre of healthcare policy and practice. What began as a single forum has grown into a landmark event that draws delegates from across India and the Asia-Pacific region.

IPS 3 in New Delhi builds on the momentum of two landmark editions, bringing together the rare disease and broader patient community under one roof to advocate for equitable, accessible, and patient-centred healthcare.

The 3rd edition broadens the agenda — moving from rare disease advocacy alone to the full continuum of patient experiences, under the theme "From Rare to Common: Uniting Patient Voices for Better Health."

Vision

A world where every patient — regardless of diagnosis — has access to knowledge, support, and quality healthcare on equal terms.

Mission

Empower patients through advocacy, policy dialogue, and multi-stakeholder partnerships that reshape the healthcare landscape.

Who Should Attend

Patients, caregivers, advocates, physicians, policymakers, pharma professionals, researchers, and media.

Venue

New Delhi, India — a fitting capital for a summit that will shape patient rights and healthcare policy for the region.

Summit Themes

IPS 3 will convene around six core themes that bridge the rare disease community with the wider patient advocacy landscape.

Patient-Centred Healthcare

Reframing health systems around the lived experience of patients — from first diagnosis through long-term disease management.

Rare Disease Policy & Access

Bridging the gap between national rare disease policies and on-the-ground patient reality across South and Southeast Asia.

Caregiver Empowerment

Recognising and supporting the invisible backbone of patient care — family members and community caregivers.

Digital Health & Innovation

Leveraging technology — telehealth, patient registries, AI-assisted diagnostics — to improve access and health outcomes.

Patient Safety & Rights

Strengthening accountability in health systems and advancing legal frameworks that protect patient rights.

Asia-Pacific Collaboration

Building cross-border networks among patient groups, research institutions, and governments to share best practices.

Summit Programme

A curated two-day programme of plenary keynotes, interactive workshops, breakout sessions, and a gala networking dinner on the evening of Day 1.

Day 1  ·  Thursday, 27 November 2026
09:00 AM
Inaugural Ceremony

Welcome address, lamp-lighting, and keynote by eminent health leaders.

10:30 AM
Plenary: Rare to Common

Panel discussion on bridging rare and common disease advocacy agendas.

12:30 PM
Networking Lunch

Curated roundtables by disease area and interest group.

02:00 PM
Parallel Workshops

Patient safety · Digital health · Caregiver wellness.

04:30 PM
Panel: Policy & Access India

Government and regulatory perspectives on patient rights.

07:00 PM
Gala Networking Dinner

Awards for outstanding patient advocacy and leadership.

Day 2  ·  Friday, 28 November 2026
09:00 AM
Plenary: Asia-Pacific Voices

Regional patient advocacy — perspectives from across Asia.

10:30 AM
Patient Stories Session

First-person narratives from patients across Asia-Pacific.

12:00 PM
Networking Lunch

Sponsor exhibitions and bilateral meetings.

01:30 PM
Breakout Sessions

Research · Funding · Media & communication for patient groups.

03:30 PM
Plenary: Road Ahead

Multi-stakeholder dialogue on healthcare access post-2026.

04:30 PM
Valedictory & New Delhi Declaration

Adoption of summit outcomes and roadmap for 2027.

Summit Documents

Download the official documents for the 3rd International Patient Summit — New Delhi, India.

Document 01
Concept Note
Overview of the summit's vision, objectives, thematic focus, and the imperative for patient-centred healthcare across the Asia-Pacific region.
Download PDF
PDF Concept Note · IPS 3
Document 02
Sponsorship Brochure
Explore partnership opportunities, sponsorship packages (Platinum to Bronze), and individual sponsorship items available for IPS 3.
Download PDF
PDF Sponsorship · IPS 3
Document 03
Summit Agenda
Full two-day programme for 27–28 November 2026 — panel discussions, workshops, breakout sessions, keynotes, and the networking dinner.
Download PDF
PDF Agenda · IPS 3

Co-Organisers

IPS 3 is presented jointly by two organisations committed to advancing patient advocacy across India and the Asia-Pacific region.

DakshamA Health
DakshamA Health

A New Delhi-based NGO empowering patients and caregivers through knowledge, advocacy, and stakeholder partnerships across India and beyond.

Visit Website
PAIR Academy
PAIR Academy

Patient Advocacy in India and the Region — building capacity among patient groups to lead and sustain advocacy in their communities.

Visit Website

Be Part of the Conversation

Registrations, sponsorships, and speaker nominations are opening soon. Visit the official IPS website or reach out to DakshamA Health for partnership enquiries.