Forventes på lager: 30-06-2020
Written by a team of experienced leaders, this book brings the most advanced knowledge and statistical methods of drug safety to the statistical, clinical, and safety community. It explains design, monitoring, analysis, and reporting issues for both clinical trials and observational studies in biopharmaceutical product development. The book addr
| Forlag | Taylor & Francis Ltd |
| Type | Bog |
| Format | Paperback / softback |
| Sprog | Engelsk |
| Udgivelsesdato | 30-06-2020 |
| Første udgivelsesår | 2020 |
| Serie | Chapman & Hall/CRC Biostatistics Series |
| Fagredaktør | Qi Jiang, H. Amy Xia |
| Originalsprog | United Kingdom |
| Sideantal | 382 |
| Indbinding | Paperback / softback |
| Forlag | Taylor & Francis Ltd |
| Sideoplysninger | 382 pages |
| Mål | 234 x 156 |
| ISBN-13 / EAN-13 | 9780367576004 |