<strong><span style="font-size: 12pt;">European Medicines Agency post-authorisation procedural </span></strong><strong><span style="font-size: 12pt;">advice for users of the centralised procedure<br /><br /></span></strong><span style="color: #888888;"><span style="font-size: 10pt;">August 2014</span><span style="font-size: 12pt;"><br /><span style="font-size: 10pt;">EMEA-H-19984/03 Rev 42</span><br /><span style="font-size: 10pt;">Human Medicines Research and Development Support</span><br /><br /><span style="background-color: #ffffff; color: #000000;"><span style="font-size: 10pt;">계속 업데이트 예정</span><br /><br /><br /><br /><span style="font-family: 굴림체, gulimche; font-size: 8pt;"><strong><span style="color: #0000ff;"><span style="color: #0000ff; font-weight: bold;"><span style="font-size: 8pt;"><span style="font-family: Verdana;"><span style="color: #0000ff;">※ 자세한 내용은 아래 </span><span style="color: #ff0000; font-weight: bold;">원문 URL</span><span style="color: #0000ff; font-weight: bold;">을 이용하시기 바랍니다.</span></span></span></span></span></strong></span> <br /></span></span></span>
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