Due diligence on candidate drugs or potential company acquisitions.

QC on regulatory documents prepared by your staff or others.

Temporary assignments when your staff are unavailable for the current workload. We can review or write reports or complete other assignments on a temporary or permanent basis. This is a great solution when you have staff on medical or maternity leave, on temporary assignment to another project, or an unexpected vacancy.

Attend scientific, FDA or ICH FDA meetings, and prepare detailed reports highlighting issues of specific concern to client.

Confidential assessments of vulnerability to scientific fraud.

Write short discussions of toxicology issues for non-toxicologists.

CRO qualification.