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Dokumento informacija
Detailed guidance for the request for authorisation of a clinical trial on a medicinal product for human use to the competent authorities, notification of substantial amendments and declaration of the end of the trial
Aprašymas Document is implemented by order No. 1A-388 of SMCA Director on 5 July 2004. Lithuanian version is available on the website http://www3.lrs.lt/cgi-bin/preps2?Condition1=237970&Condition2=
