Chair

Ms. Suneela Thatte

Vice President and Head R&D India

(Merck KGaA)

Co-chair

Mr. Ajit Nair

Head Regulatory Sciences

(Bristol Myers Squibb)

Workstream Member

Mr. Prajakk Barde

Chief Medical Officer,
(Med Indite Communications)

Workstream Member

Ms. Amita Bhave

Director Regulatory Affairs,
(Astra Zeneca Pharma Ltd.)

Workstream Member

Ms. Charu Gautam

Sr. Dir. Med. Affairs & Strategy,
(IQVIA)

Workstream Member

Mr. Gaurav Mathur

Senior Director, Regulatory Affairs,
(Paraxel)

Workstream Member

Mr. Sudipto Chatterjee

Medical Director India & EFM,
(Merck KGaA)

Workstream Member

Mr. Sandesh Sawant

Head, Clinical Trials,
(Cipla Limited)

Workstream Member

Ms. Bhawana Awasthy

VP Medical Mgmt & GM,
(Syneos Health India)

Workstream Member

Mr. Kiran Marthak

Dir. Med Affairs/Ph1 & Reg Affairs,
(Veeda Lifesciences)

Objective

Create awareness, generate interest and address capability building and expertise in the domain of early phase and translational research

Key Focus Areas

• Knowledge Sharing and Capacity Building
• Regulatory Advocacy
• Spreading awareness through collaboration

ISCR TRWG Agenda:

• Provide a platform for Clinical Research professionals involved in early clinical development and translational research to collaborate and exchange ideas, share best practices, and stay updated with latest industry trends.
• Build capacity through workshops, webinars, or any other format for early drug development and translational research concepts to advance knowledge base.
• Create awareness about the latest developments in the early clinical development arena.
• Build a strong fraternity in India for early phase and translational research space and stay at par with the latest trends and standards in the Clinical Research industry.