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Our Goal

To accelerate translation of research from bench to bedside by providing services that support pre-clinical studies and regulatory submissions. These services are:
  • Confidential
  • Focused
  • Performed collaboratively with the investigator

Available Services

  • Preclinical study planning & regulatory support
  • Pharmacology & toxicology services
  • Manufacturing of small molecules and non-biologics
  • Manufacturing of biologics
The SMARTT Program Workflow spans the following main phases: request services, NHLBI approval process, services implementation, translation and therapy.

Science Moving towArds Research Translation and Therapy

SMARTT Program Logo

Service Request Overview

  • Select the "Submit SMARTT Application" link above
  • Complete the Request for Services Application (RSA)
  • NHLBI and members of an external Scientific Review Board evaluate the application for merit and feasibility
  • Approved RSAs are assigned the appropriate program resources and the project is initiated
  • After service completion, deliverables are provided to the investigator and the project is terminated

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National Heart, Lung, and Blood Institute National Institutes of Health Department of Health and Human Services USA.gov