Proposal pdf uji sterilitas
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Transcript of Proposal pdf uji sterilitas
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One Day Seminar
Sterility Test Validation
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WHO TRS 530 (1973), WHO TRS 872 (1998),
Farmakope Indonesia, United States
Pharmacopoeia, European Pharmacopoeia,
Indian Pharmacopoeia, Chinese Pharmacopoeia
dan semua farmakope di dunia menyatakan
bahwa produsen sediaan steril diwajibkan
melakukan uji sterilitas dan validasinya untuk
menjamin produk bebas dari mikroorganisme
yang tidak diinginkan
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1. Peserta paham akan konsep penting uji sterilitas dan
validasinya
2. Peserta mengetahui pola metode dan pengembangan uji
sterilitas
3. Peserta mampu dan trampil mendisain validasi uji sterilitas
4. Peserta memiliki kompetensi dalam mengevaluasi hasil
validasi uji sterilitas
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1. Mikrobiologist / QC Staff
2. Teknisi Laboratorium Riset ( R & D )
3. QA Staff
4. Tenaga Pengajar
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1. Industri Farmasi 2. Kampus / Perguruan Tinggi
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Hotel berbintang - Bogor
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27 November 2014 09.00 s/d 16.00 WIB
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Biaya : Rp. 1.000.000 / peserta -Sudah termasuk sertifikat, materi, makan siang, coffee break
-Belum termasuk biaya akomodasi dan Transportasi