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  • ¡°Providing as much clinical information for patients¡±
  • by Lee, Tak-Sun | translator Byun Kyung A | Dec 5, 2019 06:23am
MFDS Director Kim Jeong-mi ¡°Securing competitiveness by tightening safety control¡±
Need to shift negative bias on clinical trial, trying to enhance review system for early stage trials
 ¡ã Director Kim Jeong-mi of Clinical Trial Management Division
Since the end of last October, the Korean Ministry of Food and Drug Safety (MFDS) has expanded scope of information on approved investigation new drug¡¯s (IND) protocol uploaded on its website.

Previously, only the names of clinical trial, sponsoring client, IND, targeting disease and clinical trial institute were publicly disclosed, but now more information, including comparison drug, contact information of the institute, subject selection and exemption standards are also uploaded online.

Anyone can now check a company¡¯s R&D progress in detail on the website, and patients can search information and actively participate in a clinical trial by contacting the clinical institute directly.

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