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Join us June 14-18, 2026
in Philadelphia, PA

Join global leaders, innovators, regulators, academics, and patient advocates in Philadelphia, PA for the DIA 2026 Global Annual Meeting. As the life sciences industry continues to evolve, this event serves as a powerful platform to connect, collaborate, and drive forward transformative solutions. Be part of the conversations shaping tomorrow—right in the heart of one of America’s most historic and inspiring cities.

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Conference Highlights

DIA 2025

Interactive sessions, keynote presentations, and hands-on workshops designed to accelerate your professional growth and expand your network.

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Comité del programa

  • Representative Invited
    Representative Invited FDA, United States
  • Sanghita  Bhattacharya, PhD
    Sanghita Bhattacharya, PhD Director Data Science Global Function
    Johnson & Johnson Innovative Medicine, United States
  • Asia  Blackwell
    Asia Blackwell Consumer Safety Officer, CBER
    FDA, United States
  • Tywnia  Brewton
    Tywnia Brewton Executive Director, Human Resources
    Astellas , United States
  • James  Buchanan, PharmD
    James Buchanan, PharmD President
    Covilance LLC, United States
  • Mandy Kaur Budwal-Jagait, MSc
    Mandy Kaur Budwal-Jagait, MSc Head of GCP
    Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom
  • Meghana  Chalasani, MHA
    Meghana Chalasani, MHA Associate Director for Clinical Trial Innovation, Office of New Drugs, CDER
    FDA, United States
  • Joan  Chambers
    Joan Chambers Independent Senior Consultant
    Tufts Center For the Study of Drug Development, United States
  • Rachel  Chasse, MS
    Rachel Chasse, MS Associate Director, Digital Science Strategy
    AbbVie, United States
  • Monica  Chiaramonte, PhD
    Monica Chiaramonte, PhD Director, Clinical Regulatory Writing
    AstraZeneca Pharmaceuticals LP, United States
  • Christine  Colvis, PhD
    Christine Colvis, PhD Director, Drug Development Partnership Programs
    National Center for Advancing Translational Sciences (NCATS), United States
  • Karen  Correa, PhD
    Karen Correa, PhD Vice President, Clinical Development Operations
    Boehringer Ingelheim, United States
  • Solange  Corriol-Rohou, DrMed, MD, PhD
    Solange Corriol-Rohou, DrMed, MD, PhD
    SCR Consulting, France
  • Stephanie Y. Crawford, PhD, MPH, MS
    Stephanie Y. Crawford, PhD, MPH, MS Professor, Pharmacy Systems, Outcomes and Policy
    University of Illinois at Chicago, United States
  • Alysha  Croker, PhD
    Alysha Croker, PhD Director, Strategic and Horizontal Policy
    Health Canada, Canada
  • Matthew  Curin, PharmD
    Matthew Curin, PharmD Sr. Dir, Head of Program Management, Therapeutic Dermatology
    Galderma, United States
  • Representative Invited
    Representative Invited FDA, United States
  • Victoria  DiBiaso, BSN, MPH, RN
    Victoria DiBiaso, BSN, MPH, RN Global Head, Patient Informed Development and Health Value Translation
    Sanofi, France
  • Megan  Doyle, JD, MPH
    Megan Doyle, JD, MPH Associate Vice President, Assistant General Counsel - Diagnostics
    Eli Lilly & Company, United States
  • Nancy  Dreyer, PhD, MPH, FISPE
    Nancy Dreyer, PhD, MPH, FISPE Founder
    Dreyer Strategies LLC, United States
  • Joseph  Dustin
    Joseph Dustin Founder and Principal
    Dauntless Eclinical Strategies, United States
  • Jennifer  Emerson, PhD, MPH, RN, PMP
    Jennifer Emerson, PhD, MPH, RN, PMP Head Quality Analytics & Risk Management
    Boehringer Ingelheim, Germany
  • Andrew  Emmett, MPH
    Andrew Emmett, MPH VP, Global Regulatory Policy and Global Intelligence
    Pfizer Inc, United States
  • Celeste  Frankenfeld Lamm
    Celeste Frankenfeld Lamm Senior Director, Global Regulatory Affairs – CMC
    Merck Sharp & Dohme LLC , United States
  • Danielle  Friend Economo, PhD
    Danielle Friend Economo, PhD Senior Director, US Head Regulatory Policy and Intelligence
    Johnson & Johnson Innovative Medicine, United States
  • David  Fryrear, MS
    David Fryrear, MS Chief Quality Officer
    Astellas, United States
  • Cheryl  Grandinetti, PharmD
    Cheryl Grandinetti, PharmD Associate Director for Clinical Policy, CDER/OC/OSI/DCCE
    FDA, United States
  • Courtney  Granville, PhD, MPH
    Courtney Granville, PhD, MPH
    United States
  • Lani  Hashimoto
    Lani Hashimoto Consultant, Patient Experience
    Hashimoto Consulting Services, United States
  • Sabine  Haubenreisser, PhD, MSc
    Sabine Haubenreisser, PhD, MSc Principal Scientific Administrator, Stakeholders and Communication Division
    European Medicines Agency, Netherlands
  • Cammilla  Horta Gomes, MA, MPharm
    Cammilla Horta Gomes, MA, MPharm Latam Regulatory Policy Lead
    Roche, Brazil
  • Stacy  Hurt, MBA, MHA
    Stacy Hurt, MBA, MHA Chief Patient Officer
    Parexel, United States
  • Huong  Huynh, PhD
    Huong Huynh, PhD Director of Regulatory Science
    Critical Path Institute, United States
  • Yatika  Kohli, PhD, MBA
    Yatika Kohli, PhD, MBA Chief Compliance and Strategy Officer
    NoNO Inc, Canada
  • Dominique  Lagrave, PharmD
    Dominique Lagrave, PharmD Chief Regulatory Officer
    Accumulus Technologies, United States
  • Elizabeth  Lange, MPH, MS
    Elizabeth Lange, MPH, MS Executive Director/ Head of Regulatory Scientific Policy
    EMD Serono, United States
  • Jingyu (Julia) Luan, PhD
    Jingyu (Julia) Luan, PhD Executive Regulatory Science Director, BioPharmaceuticals R&D
    AstraZeneca, United States
  • Demetra  Macheras, MBA
    Demetra Macheras, MBA Director, Regulatory Policy and Intelligence - Regulatory Affairs
    AbbVie, United States
  • David  Meats
    David Meats Director, Regulatory Services & Medical Affairs Management
    Certara, United States
  • Timothe  Menard, PharmD, MSc
    Timothe Menard, PharmD, MSc Global Head, Quality Excellence Digital | Bioethics Ambassador
    F. Hoffmann-La Roche Ltd, Switzerland
  • Pallavi  Mishra-Kalyani, PhD, MS
    Pallavi Mishra-Kalyani, PhD, MS Deputy Division Director, DBV, OB, CDER
    FDA, United States
  • May F Mo, MBA, MS
    May F Mo, MBA, MS Executive Director, Biostatistics
    Amgen, United States
  • Monica  Munoz, PharmD, PhD
    Monica Munoz, PharmD, PhD Division Director, Division of Pharmacovigilance-I, OSE, CDER
    FDA, United States
  • Lauren  Oliva, PharmD, RPh
    Lauren Oliva, PharmD, RPh US Regulatory Policy Lead
    Biogen, United States
  • Representative Invited
    Representative Invited FDA, United States
  • Vada  Perkins, DrSc, MSc
    Vada Perkins, DrSc, MSc Vice President, Global Head of Regulatory Intelligence & Policy
    Boehringer Ingelheim, United States
  • Regina Lynn  Preciado
    Regina Lynn Preciado VP, Content Strategy Solutions
    Content Rules, Inc., United States
  • Ranjini  Prithviraj, PhD, PMP
    Ranjini Prithviraj, PhD, PMP Director, Global Medical Affairs, Publication Management
    Regeneron, United States
  • Kim  Ribeiro, MS
    Kim Ribeiro, MS Director Patient Experience & Engagement
    Boehringer Ingelheim, United States
  • Leslie  Sam
    Leslie Sam President
    Leslie Sam and Associates, LLC, United States
  • Earl  Seltzer, MBA
    Earl Seltzer, MBA Senior Director, Partnerships and Innovation
    CTI, United States
  • Anjali  Shah, PharmD
    Anjali Shah, PharmD Executive Director, Business Capabilities and Innovation, WWPS
    Bristol-Myers Squibb Company, United States
  • Nancy Pire Smerkanich, DrSc, MS
    Nancy Pire Smerkanich, DrSc, MS Assistant Professor Regulatory & Quality Sciences
    University of Southern California School of Pharmacy, United States
  • Cary  Smithson, MBA
    Cary Smithson, MBA Managing Partner
    LeapAhead Solutions, Inc., United States
  • Benjamin  Stevens, PhD, MPH
    Benjamin Stevens, PhD, MPH Director CMC Policy and Advocacy
    GlaxoSmithKline, United States
  • Nancy Linda Styple
    Nancy Linda Styple Project Management Leader
    Bayer AG, United States
  • Ling  Su, PhD
    Ling Su, PhD Research Fellow
    Yeehong Business School, China
  • John Z. Sun, PhD, MBA, PMP
    John Z. Sun, PhD, MBA, PMP Program Lead, Global Clinical Operation, Development
    Novartis Pharmaceuticals Corporation, United States
  • Michael  Torok, PhD
    Michael Torok, PhD Vice President, Global Head of Quality Assurance Programs
    Genentech, A Member of the Roche Group, United States
  • Phil  Tregunno
    Phil Tregunno Deputy Director - Patient Safety Monitoring
    Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
  • Representative Invited
    Representative Invited Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • James  Valentine, JD, MHS
    James Valentine, JD, MHS Director
    Hyman, Phelps & McNamara, PC, United States
  • James  Wabby, MHS
    James Wabby, MHS Global Head, Regulatory Affairs, Emerging Technologies and Combination Products
    AbbVie, United States
  • Paula  Walker, MA
    Paula Walker, MA Global Head of Risk Based Quality Management
    Roche Products Ltd., United Kingdom
  • Robin  Whitsell
    Robin Whitsell President
    Whitsell Innovations, Inc., United States
  • Amira Deia Younes
    Amira Deia Younes Director-Eastern Europe, Middle East & Africa (EEMEA) Global Regulatory Policy
    MSD, United Arab Emirates
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