PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – SANITASI

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – SANITASI NO VERSI ASLI VERSI TERJEMAHAN 61 The sanitation of clean areas is particularly important. They should be cleaned thoroughly in accordance with a written programme. Where disinfectants are used, more than one type should be employed. Monitoring should…

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – PERALATAN

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – PERALATAN NO VERSI ASLI VERSI TERJEMAHAN 56 A conveyor belt should not pass through a partition between a grade A or B area and a processing area of lower air cleanliness, unless the belt itself is continually sterilised (e.g.

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – FASILITAS (BANGUNAN)

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – FASILITAS (BANGUNAN) NO VERSI ASLI VERSI TERJEMAHAN 46 In clean areas, all exposed surfaces should be smooth, impervious and unbroken in order to minimise the shedding or accumulation of particles or micro-organisms and to permit the repeated application of…

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – PERSONALIA

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – PERSONALIA NO VERSI ASLI VERSI TERJEMAHAN 36 Only the minimum number of personnel required should be present in clean areas; this is particularly important during aseptic processing. Inspections and controls should be conducted outside the clean areas as far…

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – PEMBUATAN SECARA ASEPTIK

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – PEMBUATAN SECARA ASEPTIK NO VERSI ASLI VERSI TERJEMAHAN 31 Components after washing should be handled in at least a grade D environment. Handling of sterile starting materials and components, unless subjected to sterilisation or filtration through a micro-organism-retaining filter…

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – TEKNOLOGI ISOLATOR

PIC/S ANEKS 1 (PEMBUATAN PRODUK STERIL) – TEKNOLOGI ISOLATOR NO VERSI ASLI VERSI TERJEMAHAN 21 The utilisation of isolator technology to minimise human interventions in processing areas may result in a significant decrease in the risk of microbiological contamination of aseptically manufactured products from the environment.