Overview

The DIA Medical Writing Conference 2025 is a premier platform designed to bring together experts, thought leaders, and professionals from the medical writing, medical, clinical & regulatory affairs, and healthcare communication domains. With the rapidly evolving landscape of regulatory writing, Scientific writing and medical communication, it is crucial to stay ahead by embracing innovation, collaboration, and technology.

This Conference will serve as a catalyst for knowledge-sharing, skill-building, and thought leadership in regulatory writing, scientific writing and medical communication. Attendees will gain insights into emerging trends, challenges, and innovations shaping the future of medical writing. From regulatory frameworks and clinical study documentation to AI-driven writing solutions and ethical publication practices, this forum will foster discussions on critical advancements and their real-world implications.

The conference will have two tracks: 1- Scientific Writing and medical communications; 2- Regulatory Writing

Additionally, the Conference will provide unparalleled networking opportunities, enabling participants to connect with peers, industry experts, and regulatory professionals. These interactions will facilitate collaboration, mentorship, and the exchange of ideas, fostering a strong professional community dedicated to advancing the field of medical writing.

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Exhibits

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Exhibits

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Who should attend?

The DIA Medical Writing Conference 2025 is designed for professionals, functional and business leaders across the pharmaceutical, life sciences, academia, and healthcare communication ecosystem, including:

Medical Writers, Scientific Communicators and Publication Specialists
Medical Affairs Professionals
Regulatory Affairs & Clinical Development Professionals
Pharmacovigilance & Safety Writing Experts
Senior Professionals & Thought Leaders in Medical Writing
Academia & Researchers involved in scientific communication
Healthcare & Life Sciences Industry Experts

Learning objectives

Enhance Excellence and Innovation – Explore cutting-edge advancements in regulatory writing, scientific writing and medical communications, including AI, automation, and evolving methodologies.

Promote Collaboration and Thought Leadership – Foster cross-functional engagement among industry experts, regulators, and academia to drive best practices and industry standards.

Address Challenges and Emerging Trends – Discuss key challenges such as data transparency, evolving regulations, global submission requirements, scientific writng and medical communications, and patient-centric writing including use of visuals/videos/interactive communication modes.

Empower Professionals with Knowledge and Skills – Provide practical learning through expert panels, case studies, and pre-conference workshops to enhance writing clarity, compliance, and impact.

Shape the Future of Medical Writing – Inspire innovation and adaptability by exploring the role of technology, regulatory evolution, and multidisciplinary collaboration in the field.

Program Committee

Pooja Phogat, Ph.D, PhD Founder and Co-CEO
Krystelis Ltd., India
Shruti MP, MSc Director-Real World Data Solutions
Parexel International, India
Annie Jose Associate Director, Medical Writing
GSK, Bengaluru, India
Shivanand Jigajinni Director- Head of India MW Operations. Global Medical Writing - DSSM
IQVIA, India
Dr. Natasha Das, MBBS Independent Medical Communications Consultant
India
Sherin Babykutty Senior Manager - Regulatory Writing
Eli Lilly Services India Private Ltd, India
Ubhayabharathi Gurunath Ad-interim Group Lead - Scientific Writing
Sanofi, India
Rajesh Pandey, MD Head, Medical Writing & Medical Affairs
Tata Consultancy Services, India