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Highlighted Speakers

Michele Weitz

Senior Director GCP, Compliance Operations, Clovis Oncology

Ann McCabe

Director, Process Excellence and Risk Management Clinical Development, Operations, Daiichi Sankyo

Karen McCarthy Schau

Director Consulting Services Health & Life Sciences, CGI

Chrysanthi Dori

Head of Direct Subject Data & Acquisition, Bayer

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 compliance 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.

Exhibit

If you have an insightful, take-away driven case study to share, we want to hear from you.

Speak

We help our media partners engage with our community of marketing leaders and decision-makers.

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