Validation of HPLC quantity determination procedure of "ibumol" suppositories
- At: 2011 FIP Congress in Hyderabad (India)
- Type: Poster
- By: TILLAEVA, Gulnora (Head Dept. of Drug And Med. Equip. Quality Control, Tashkent, Uzbekistan)
- Co-author(s): Ganieva, Khilola (Tashkent Pharmaceutical Inst., Tashkent, Uzbekistan)
Aim: validation of HPLC quantity control procedure of "Ibumol" suppositories is determined on validative characteristic: Method: for HPLC validation procedure of "Ibumol" suppositories the extraction of investigated substances from forming substances has been preliminary conducted. For extraction hexan, 5% solutions of sodium carbonate were used... The access to the whole abstract and the presentation file is available to FIP members and to congress participants of that specific congress.