National Capacity-Building Workshop on Rare Disease Drug Development: Science, Regulation & Patients

12–14 November 2026
Venue: Indian National Science Academy (INSA), New Delhi

The National Capacity-Building Workshop on Rare Disease Drug Development: Science, Regulation & Patients brings together participants working in clinical research, drug development, regulation and related fields.

Organizing institutions: Tata Institute for Genetics and Society (TIGS), Medanta Institute of Education and Research (MIER), and World Without GNE Myopathy (WWGM).

Knowledge partner: Indian Society for Clinical Research (ISCR).

Workshop modules

Who should attend?

The workshop is intended for postgraduate students, research scholars/scientists, medical doctors, regulatory professionals, PAGs (patient advocacy groups), and other young professionals in these areas:

Inauguration

Speakers

Panelists

Registration and contact

The brochure states that seats are limited. Scan the registration QR code on either brochure page below to register.

For enquiries, email info@tigs.res.in .

Brochure

Download the original two-page brochure (PDF, 681 KB) .

Select either image to view it at full size. The workshop details and speaker lists are also provided as readable text above.

Workshop brochure: Rare Disease Drug Development—Science, Regulation & Patients, November 12–14, 2026 at INSA, New Delhi. Includes modules, intended audience and registration QR code; details are transcribed above.

Brochure speaker list, with inauguration participants, speakers and panelists and their affiliations, transcribed above. Includes the registration QR code.