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Presenting Speakers:

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Highlighted Speakers

JoAnn Pfeiffer

Director/Associate Professor, Clinical Research Management & Regulatory Science Masters Programs, Arizona State University

Fran Ross

TMF Ref Model SC Member, Consultant, Life Sciences R&D, CGI

Cristin Palumbo Freeman

MPH, MBE, Associate Principal Scientist, Global Genomics Policy, Process and Compliance, Merck Research Laboratories

Stephanie Viscomi

Associate Director, Clinical Trial Office, ImmunoGen, Inc.

SIX REASONS WHY THE TRIAL MASTER FILE AND CLINICAL DOCUMENT MANAGEMENT CONFERENCE IS A MUST ATTEND EVENT

People, Process & Technology.

Discuss an integrated approach to ensuring accurate and compliant TMF and clinical documents.

Location. Location. Location.

Located in Anaheim, CA, the Trial Master File + Clinical Document Management Conference is located centrally to those in the industry.

Stay Ahead of the Game.

Featuring deep dives into emerging technologies impact on TMF and industry trends, you won’t get left behind.

Be Inspection Ready, 100% of the Time

Learn best practices, metrics and KPIs to ensure that your TMF is accurate, updated and in compliance regardless of when it’s inspection time.

Make the move to eTMF.

In depth how to’s and case studies that help ensure your migration to eTMF is speedy, accurate and trouble free.

Sponsor, Site or CRO – we’ve got you covered.

With two tracks and 4 workshops, our wide range of topics will exceed your requirements, regardless of your role in the industry.

How to Participate

We can customize sponsorship and exhibit opportunities for you to create an unforgettable company presence.

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Trial Master File Conference

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