TMF management is becoming increasingly specialised. This specialisation is attributable to a host of factors – globalisation; a matrix of overlapping regional and international regulations; emerging technologies; and interdependence of TMF professionals and professionals in other functional units.

We are expanding the TMF Institute globally to meet the growing demand for targeted professional development, training and education for the TMF professionals and allies. We created the TMF Institute by incorporating what participants like most about the TMF Summit series’ workshops into an objective-driven professional growth and learning opportunity. Each of the TMF Institute daylong courses provide information and develop skills essential to specific to a specialized job function or level or responsibility

The TMF Institute consists of a slate of four courses to meet the professional development and educational needs growing TMF community. The instructors and all facets (e.g., content, activities, discussion topics) of each course are determined by what participants need to know and be able to do to excel in a particular purview or echelon.

Who Should Participate

Professionals from pharmaceutical, biotech, and medical device organisations as well as CROs, vendors, and eTMF/TMF service providers having or seeking responsibilities in the following areas:

  • TMF/eTMF Systems Management
  • Clinical Document Management
  • Clinical Trial Documentation
  • Clinical Trial Administration
  • Clinical/TMF Project Management
  • Quality Control/Quality Management
  • Clinical Operations
  • Clinical Research Coordination/Management
  • Regulatory Affairs/Operations
  • Business
  • Trial Records Management
  • Clinical Process
  • Clinical Trial Compliance
  • Clinical Development
  • Quality Assurance/Control/Operations
  • R&D Quality Management
  • Strategic Operations and Planning
  • Global Development
  • R&D IS Management
  • Archives

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