PharmaNet study monitors are specifically trained in the complexities of the multidisciplinary trial environment. Their services include:
 Monitoring the development of study procedures |
| Reviewing source documents |
| Confirming patient eligibility |
| Tracking patient compliance |
| Managing study supply inventories |
| Reporting adverse events |
| Monitoring regulatory compliance |
| Maintaining regulatory documentation
|
Site visits provide the opportunity to discuss recruitment strategies, identify potential problems, and compile direct feedback on performance.
504 Carnegie Center, Princeton, NJ 08540