 |
ISBN
| 9781119120919 | |
DDC
| 615.19 | |
Nhan đề
| Analytical chemistry an introduction to pharmaceutical GMP laboratory / Kim Huynh-Ba (editor) | |
Lần xuất bản
| 1st ed. | |
Thông tin xuất bản
| Hoboken, NJ : John Wiley & Sons, Inc., 2022 | |
Mô tả vật lý
| xxx, 386 pages. : illustrations ; 24 cm. | |
Phụ chú
| Includes index. | |
Tóm tắt
| Analytical Testing for the Pharmaceutical GMP Laboratory presents a thorough overview of the pharmaceutical regulations, working processes, and drug development best practices used to maintain the quality and integrity of medicines. With a focus on smaller molecular weight drug substances and products, the book provides the knowledge necessary for establishing the pharmaceutical laboratory to support Quality Systems while maintaining compliance with Good Manufacturing Practices (GMP) regulations. | |
Từ khóa tự do
| Industrie pharmaceutique | |
Từ khóa tự do
| Industrie pharmaceutique qualite controle | |
Từ khóa tự do
| Pharmaceutical chemistry | |
Từ khóa tự do
| Drug development | |
Từ khóa tự do
| Analytical chemistry | |
Từ khóa tự do
| Drugs testing | |
Từ khóa tự do
| Pharmaceutical industry quality control | |
Từ khóa tự do
| Chemistry, pharmaceutical | |
Khoa
| Khoa Dược | |
Tác giả(bs) CN
| Huynh-Ba, Kim | |
Địa chỉ
| 200Q7_Kho Mượn(1): 091073 |
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| 00000nac#a2200000u##4500 |
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| 001 | 48751 |
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| 005 | 202405161145 |
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| 008 | 240516s2022 nju eng |
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| 009 | 1 0 |
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| 020 | |a9781119120919|c4631000 |
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| 040 | |aNTT |
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| 041 | |avie |
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| 044 | |avm |
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| 082 | |a615.19|bA5329|223 |
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| 245 | |aAnalytical chemistry an introduction to pharmaceutical GMP laboratory / |cKim Huynh-Ba (editor) |
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| 250 | |a1st ed. |
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| 260 | |aHoboken, NJ : |bJohn Wiley & Sons, Inc., |c2022 |
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| 300 | |axxx, 386 pages. : |billustrations ; |c24 cm. |
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| 500 | |aIncludes index. |
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| 520 | |aAnalytical Testing for the Pharmaceutical GMP Laboratory presents a thorough overview of the pharmaceutical regulations, working processes, and drug development best practices used to maintain the quality and integrity of medicines. With a focus on smaller molecular weight drug substances and products, the book provides the knowledge necessary for establishing the pharmaceutical laboratory to support Quality Systems while maintaining compliance with Good Manufacturing Practices (GMP) regulations. |
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| 541 | |aMua |
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| 653 | |aIndustrie pharmaceutique |
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| 653 | |aIndustrie pharmaceutique qualite controle |
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| 653 | |aPharmaceutical chemistry |
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| 653 | |aDrug development |
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| 653 | |aAnalytical chemistry |
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| 653 | |aDrugs testing |
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| 653 | |aPharmaceutical industry quality control |
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| 653 | |aChemistry, pharmaceutical |
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| 690 | |aKhoa Dược |
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| 691 | |aDược học |
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| 700 | |aHuynh-Ba, Kim|eeditor |
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| 852 | |a200|bQ7_Kho Mượn|j(1): 091073 |
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| 856 | 1|uhttp://elib.ntt.edu.vn/documentdata01/2 tailieuthamkhao/600 congnghe/anhbiasach/48751-analytical testing for the pharmaceutical gmp laboratorythumbimage.jpg |
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| 890 | |a1|b0|c1|d2 |
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Q7_Kho Mượn
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