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Volume 69, August 2008 |
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Tips & Tools One of the common problems facing companies conducting global clinical trials is knowledge of the regulatory requirements in each country. Global Language Solutions® provides regulatory consulting services that can result in an investigational drug entering clinical trials sooner by shortening the labeling and translation processes. The service, which is provided by industry expert Dr. David Bernstein, is estimated to shorten the regulatory compliance, translation, and back translation process from 2-3 weeks to less than one week. More importantly it will minimize or eliminate any delays to the labeling process should the local or regional Ministry of Health request additional label text that is required in its region. For more information about GLS and our pharmaceutical and clinical research translation and regulatory compliance services, contact us. |
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