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Old 05-19-2006, 08:46 PM
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Default Free Regulatory Roadmap Poster for Clinical Trials

Free Regulatory Roadmap Poster

Trying to find your way through the maze of clinical trial regulations? Not sure which record and signature requirements are important?

In easy-to-read, color-coded format, the free "Regulatory Roadmap to U.S. Clinical Trials" by SEC Associates, Inc. and Phase Forward, helps you navigate the clinical trial process easily by highlighting the major stages of clinical investigation and the important record and signature requirements in U.S. Good Clinical Practices (GCP), 21 CFR Part 11, and the International Conference on Harmonisation (ICH) E6 Guideline for Good Clinical Practice. The roadmap also notes key recordkeeping references and GCP regulation summaries.

While the roadmap focuses mainly on drugs submitted for approval by the U.S. FDA, the global significance of the U.S. GCP and ICH E6 references make the roadmap a valuable tool for international clinical trials, as well.

So stop struggling to understand the regulations governing clinical trials -- Let SEC Associates, Inc. and Phase Forward show you the way. Complete the following brief form, and we'll send your free regulatory roadmap today.

Note: This is a full size wall poster (26" x 39") and requires a complete mailing address.

www.secassociates.com/regulatory_roadmap/

Request form is near bottom of page
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