DIREKTIF PENGUATKUASAAN KEPERLUAN KAJIAN BIOEKUIVALENS (BE) BAGI PRODUK GENERIK DALAM BENTUK DOS ORAL TABLET/KAPSUL YANG BERSIFAT EFFERVESCENT, DISPERSIBLE, ORODISPERSIBLE, SUBLINGUAL, BUCCAL DAN CHEWABLE YANG MENGANDUNGI BAHAN AKTIF RACUN BERJADUAL

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Date: 23 February 2015

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National Pharmaceutical Regulatory Agency (NPRA)
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