Clinical Quality Assurance Roles and Responsibilities for Auditors and Managers

United States
Now you can learn how to FDA-proof your CQA audits … eliminate costly mistakes … and avoid FDA warning letters that say:

“You failed to obtain and document that valid informed consent was obtained for each of the subjects enrolled in the study as required by stated regulations.”


One Registration -Raleigh, NC -Feb. 27-28, 2013