CSDL sách
- Handbook of pharmaceutical manufacturing formulations: Sterile products
- Tác giả: Safaraz K. Niazi
- Nhà xuất bản: Informa healthcare - New York
- Năm xuất bản: 2009
- Số trang:434 p.
- Kích thước:28 cm.
- Số đăng ký cá biệt:31373
- ISBN:9781420081305
- Mã Dewey:615.19
- Đơn giá:0
- Vị trí lưu trữ:03 Quang Trung
- Ngôn ngữ:English
- Loại tài liệu:Sách Tham Khảo
- Đang rỗi/ Tổng sách:1/1
- Từ khóa:Drug compounding handbooks, technology, pharmaceutical
- Chủ đề: Drugs--Handbooks
- Chuyên ngành: Khoa Dược
- Tóm tắt: No other area of regulatory compliance receives more attention and scrutiny by regulatory authorities than the regulation of sterile products, for obvious reasons. With the increasing number of potent products, particularly the new line of small protein products, joining the long list of proven sterile products, the technology of manufacturing sterile products has evolved into a very sophisticated industry. Highlights from Sterile Products, Volume Six include: formulations of sterile dosage forms, regulatory filing requirements of sterile preparations, and cGMP compliance, all of which are tied together in the final preparation of the CMC sections of regulatory applications specifications of a manufacturing facility to manufacture compliant sterile products.
- Sách điện tử:http://thuvienso.duytan.edu.vn/handle/123456789/297697
Sách cùng chuyên ngành