Are in situ monitoring and testing documents, including documents related to the experimental study facility required to be included in the LSN?
Related Questions
- If the sponsor has their own facility for conducting phase I Clinical Trials and the PI is employee of the sponsor Does the monitor has any role in monitoring?
- If the sponsor has their own facility for conducting phase I Clinical Trials and the PI is employee of the sponsor Does the monitor has any role in monitoring?
- Are in situ monitoring and testing documents, including documents related to the experimental study facility required to be included in the LSN?
- If sterilizing an implantable device, should users perform biological monitoring (spore testing) more frequently?
- How often should I perform biological monitoring (BI) (spore testing)?
- How often should I perform biological monitoring (BI) (spore testing)?
