Service at a glance
| Item | Details |
|---|---|
| Provider | Hopkins MedTech Compliance |
| For | Clinical study sponsors |
| Work | Study plans, coordination and progress reporting |
| Rules and standards | Study protocol and applicable GCP requirements |
Clinical project management covers study plans, project coordination and status reporting. Scope and responsibilities are agreed for each study.
● Develop a specific research plan to thoroughly manage and monitor each project, as well as monitor risk management
● Narrow down all research needs at the local level - including central labs, warehouses and other third parties (on request)
● Organize, plan and hold investigator meetings
● Project status tracking and client reports
● Negotiate budgets and execute contracts with research sites to provide the most cost-effective option.
● conduct initial and regular research group meetings, to ensure effective planning, organization, and conduct of research
● Manage all research related issues in all phases of the trial
Service information adapted from the original source ↗.
Read the original website record