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3.3 Apakah tersedia papan nama yang mencantumkan nama PBF di depan
lokasi kantor dan gudang PBF? m 3.4 Apakah tersedia area dan akses
terpisah untuk penerimaan dan pengeluaran barang untuk meminimalisir
risiko campur baur obat dan diversi obat? M 3.5 Apakah tersedia POB
yang mengatur akses personil terhadap area penerimaan, penyimpanan dan
pengiriman? m 3.6 Apakah luas ruang penyimpanan memadai? M 3.7 Apakah
kebersihan dan kerapian bangunan dijaga serta dipelihara sesuai POB? m
3.8 Apakah gudang penyimpanan obat dapat menjamin mutu obat (bebas
banjir, penerangan cukup, suhu yang terkondisikan sesuai persyaratan
lain penyimpanan obat)? M 3.9 Apakah dilakukan pemetaan suhu di gudang
penyimpanan? M 3.10 Apakah suhu dan kelembaban udara di ruang
penyimpanan dimonitor sesuai dengan yang dipersyaratkan masing-masing
produk menggunakan alat ukur yang terkalibrasi? M 3.11 Apakah mempunyai
sistem pengendalian hama (
pest control
) dan terdokumentasi? M 3.12 Apakah tersedia palet atau peralatan lain
yang menjamin obat dan/atau bahan obat tidak bersentuhan langsung dengan
lantai? M
4. OPERASIONAL 4.1 Pengadaan
4.1.1 Apakah ada POB pengadaan? M 4.1.2 Apakah dilakukan
kualifikasi/rekualifikasi pemasok (dokumen atau audit lapangan sesuai
dengan analisis risiko)? M 4.1.3 Apakah seluruh pengadaan dari sumber
yang sah? C 4.1.4 Apakah pengadaan berdasarkan surat pesanan? (untuk
pengadaan dari PBF cabang ke Pusat, surat pesanan dapat berupa surat
pesanan elektronik) M 4.1.5 Apakah surat pesanan diverifikasi oleh
penanggung jawab, mencantumkan nama jelas dan nomor SIK dan distempel
perusahaan atau bagi PBF cabang penanggung jawab memiliki otoritas
dalam melakukan pesanan melalui elektronik? M 4.1.6 Apakah memiliki
sistem dokumentasi pengadaan yang tervalidasi untuk mencegah terjadinya
pengadaan di luar sistem yang ditetapkan, serta mampu telusur ? M 4.1.7
Apakah PBF melakukan impor obat dan/atau bahan obat? Jika ya lanjutkan
dengan 4.1.8 s/d 4.1.9 N/A
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