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Pharmaceutical Process Scale Up: Vol. 157


This book deals with a subject that is both fascinating and vitally important for the pharmaceutical industry-the procedures of transferring the ...

  • CodeCallNoLokasiKetersediaan
    01021060500074Tersedia
  • Perpustakaan
    Fakultas Farmasi
    Judul Seri
    -
    No. Panggil
    615.1-2 Lev P
    Penerbit Taylor & Francis : New York.,
    Deskripsi Fisik
    xxiii, 538 hal. Ilus. ; 23,5 cm Index. Hlm 531 - 5
    Bahasa
    Indonesia
    ISBN/ISSN
    978-1-57444-876-4
    Klasifikasi
    615.1-2 Lev P
    Tipe Isi
    -
    Tipe Media
    -
    Tipe Pembawa
    -
    Edisi
    NULL
    Subyek
    Info Detil Spesifik
    -
    Pernyataan Tanggungjawab
  • This book deals with a subject that is both fascinating and vitally important for the pharmaceutical industry-the procedures of transferring the results of research and development (R&D) obtained on laboratory scale to the pilot plant and finally to production scale. The book is divided to 15 chapters. Chapter 1 discuss dimensional analysis and scale-up in theory and industrial application. Chapter 2 discuss engineering approaches for pharmaceutical process scale-up, validation, optimization, and control in the process and analytical technology (PAT) era. Chapter 3 discuss a parenteral drug scale-up. Chapter 4 discuss non-parenteral liquids and semisolids. Chapter 5 discuss scale-up considerations for biotechnology-derived products. Chapter 6 discuss batch size increase in dry blending and mixing. Chapter 7 discuss powder handling. Chapter 8 discuss scale-up in the field of granulation and drying. Chapter 9 discuss roller compaction scale-up. Chapter 10 discuss batch size increase in fluid-bed granulation. Chapter 11 discuss scale-up of extrusion and spheronization. Chapter 12 discuss scale-up of the compaction and tableting process. Chapter 13 discuss practical considerations in the scale-up of powder-filled hard shell capsule formulations. Chapter 14 discuss scale-up of film coating. Chapter 15 discuss innovation and continous improvement in pharmaceutical manufacturing.
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