Fran Ross, Principal Consultant, Clin/Reg Optimization | Paragon Solutions, is Chair of the TMF RM Survey Team and Lead for Asia Pacific SubTeam and can be reached at firstname.lastname@example.org
TMF Reference Model Standard = Process Efficiency
One of the many activities across the clinical development cycle that is non-negotiable is the creation, collection, management, and storage of the documents that are contained in the Trial Master File.
TMF Reference Model - The Case for Standards
The research and development process continues to be long, complex and costly. Sponsors are challenged with filling pipelines, conducting complex global clinical trials and complying with requirements for additional safety and efficacy data.
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