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 |
UnitCount | 1 |
EANs | 9781930624375 |
ReleaseDate | 0000-00-00 |