What Do Tom Cruise and TMF Management Have in Common?
Tuesday July 9th, 2019
Clinical trial document management is no joking matter! As a TMF professional, you understand the seriousness and weight held by compliant and complete study files. So, how does your organization identify risk within your TMF processes?
ExL’s Trial Master File Institute — Philadelphia features a full-day workshop focused on developing and executing strategic plans that can correct gaps in the completeness, non-compliance, and quality of your organization’s TMF processes. Lead instructor Donna Dorozinsky, President of Just In Time GCP, has prepared a robust workshop that will arm attendees with strategic approaches for correcting some of the most common issues in TMF management.
RISK IDENTIFICATION: Develop and Execute a Strategic Plan to Correct Gaps in Processes or Completeness, Non-Compliance or Gap in Procedural Document, and Other Quality Issues
- Lead: Donna Dorozinksy, President, JUST IN TIME GCP
- Joanne Malia, Director, Clinical Documentation Management, REGENERON
- Vinay Pasachuri, Practice Head — Life Sciences, PHARMA TEK SOLUTIONS
The two-day Institute offers a total of four seminars for attendees to choose from, including TMF Essentials, Technology Enhancements, and Compliant Documentation. I urge you to download the full program to review all the topics being covered by our expert instructors.
Send members from your team to each workshop and save 25% with our group discount.
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