Current Good Manufacturing Practices
Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents: Code of Federal Regulations Title 21: Concise Desk Reference
FDA Regulations and Associated Guidance Documents: - Part 11 Electronic Records; Electronic Signatures - Part 26 Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and the European Community - Part 200 Drugs General - Part 207 Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution - Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs - Part 211 Current Good Manufacturing Practice For Finished Pharmaceuticals - Part 600 Biological Products: General - Part 807 Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices - Part 820 Quality System Regulation Reference Tools: - Glossaries combined in one location - GMP Keyword Index for 21CFR211 - Combined Index for all documents
- ISBN 13 : 9781449505233
- ISBN 10 : 1449505236
- Judul : Current Good Manufacturing Practices
- Sub Judul : Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents: Code of Federal Regulations Title 21: Concise Desk Reference
- Pengarang : Mindy J. Allport-Settle,
- Kategori : Reference
- Penerbit : CreateSpace
- Bahasa : en
- Tahun : 2009
- Halaman : 634
- Halaman : 634
- Google Book : http://books.google.com/books?id=NWUEQgAACAAJ&dq=intitle:Good+Manufacturing+Practice&hl=&source=gbs_api
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Ketersediaan :
FDA Regulations and Associated Guidance Documents: - Part 11 Electronic Records; Electronic Signatures - Part 26 Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and ...