Description
This <b>practical, introductory</b> course was designed to provide a
mechanism for those interested in understanding the basic
requirements for auditing in the pharmaceutical and related
industries.<br><br>
The course presents an introduction to the evolutionary
process of FDA regulations and describes in detail the latest
FDA initiatives in the inspection process. It provides a road
map for auditors in setting up a cGMP audit trail from
beginning to end. Specific compliance aspects like change
control, outsourcing, and validation will be presented as they
pertain to the audit function. The course will consist of
lectures, interactive discussions and a hands-on workshop<br><br>
Attend this course and its companion course, <b>Preparing for and Surviving an FDA Inspection</b>, ID# 187 (Offering # 0808-306) and save $300 off combined regular tuition.
01/01/0001
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Biotech
Course Category
Address
New Brunswick, NJ
New Brunswick,