The CRC's Guide to Coordinating Clinical Research
The CRA's Guide explains the role and responsibilities of a CRA, informs readers of the history of the regulations, explains in detail the research process and describes the regulations and GCPs that govern clinical research.
Book topics:
- Preparing for a study and selecting investigators
- Obtaining and monitoring informed consent
- Preparing for a monitoring visit
- Recruiting and retaining study subjects
- Conducting adverse event and safety monitoring
- Preparing for audits and detecting fraud
| Country | USA |
| Manufacturer | CenterWatch |
| Binding | Paperback |
| EANs | 9781930624375 |
| ReleaseDate | 0000-00-00 |