Unique in approach, exhaustive in coverage: this book provides information usually not available to scientists. It explains the basic scientific and technical requirements which apply to the patenting and registration of human or veterinary vaccines and therapeutic biomedicinal products. Pragmatic and practice-oriented, it helps users select and manage successfully the most attractive research and development projects. An impressive number of topics is covered, including: * planning and managing product development * product development phases * requirements for a patentable invention * patent costs * user safety * ecotoxicity The book will rapidly pay for itself by more successful fund applications, increased protection and remuneration of intellectual property, and by faster and more efficient product development.... 21, 29 Peri-lpostnatal toxicity: see Toxicity, reproductive Personnel cost 24-26 Peru 75 Pharmacodynamic 106, 121, 123-124, 136, 138, 140 ... Potency 139, 144, 145 Prelicencing serials 44, 144, 145 Prices of pharmaceuticals 12 Prior art see Patent Process development 43, 44, ... 3-5, 31 Residues 106, 133-134, 142- 145 Tanzania 88 Teratology: see Toxicity, reproductive Thailand 75 Togo 88 Index 171.
|Title||:||Research and Development of Vaccines and Pharmaceuticals from Biotechnology|
|Publisher||:||John Wiley & Sons - 2008-07-11|