Conference Details

A TMF is more than a living archive of a clinical trial progress; it is a system required by regulatory authorities and is critical for clinical oversight. By developing, implementing and utilizing a sound TMF plan, you will be able to monitor a trial as it advances, ensure high-quality documents and prepare your organization for an inspection at any stage. Additionally, by creating a TMF process, the clinical trial sponsors, CRO and site will be able to demonstrate their continued adherence to GCP during the trial

Date :

Place : United States, Orlando

Website :

Contact Person:Paula Edwards

Description:

A TMF is more than a living archive of a clinical trial’s progress; it is a system required by regulatory authorities and is critical for clinical oversight. By developing, implementing and utilizing a sound TMF plan, you will be able to monitor a trial as it advances, ensure high-quality documents and prepare your organization for an inspection at any stage. Additionally, by creating a TMF process, the clinical trial’s sponsors, CRO and site will be able to demonstrate their continued adherence to GCP during the trial

A TMF is more than a living archive of a clinical trial progress; it is a system required by regulatory authorities and is critical for clinical oversight. By developing, implementing and utilizing a sound TMF plan, you will be able to monitor a trial as it advances, ensure high-quality documents and prepare your organization for an inspection at any stage. Additionally, by creating a TMF process, the clinical trial sponsors, CRO and site will be able to demonstrate their continued adherence to GCP during the trial will be held in Orlando,United States on date 2018-01-24

Deadline for abstracts/proposals : 4th January 2018

Organized By :New York Events List

Keynote Speakers :

Conference Highlights :Learn from case studies and best practices for designing and implementing a TMF plan for global trials and inspectional readiness. Networking and learn with over 250 TMF colleagues. Hear updates on the DIA reference model and MCC’s metrics working group.

Venue :Orlando, FL, United States

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A TMF is more than a living archive of a clinical trial progress; it is a system required by regulatory authorities and is critical for clinical oversight. By developing, implementing and utilizing a sound TMF plan, you will be able to monitor a trial as it advances, ensure high-quality documents and prepare your organization for an inspection at any stage. Additionally, by creating a TMF process, the clinical trial sponsors, CRO and site will be able to demonstrate their continued adherence to GCP during the trial

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