Spotlight on Science Meetings, Conferences and Events brings you information on the following: Global Chemical and Biochemical Engineering Meeting
An effective quality system program, along with several regulatory requirements, includes the documentation and evaluation of changes made to validated equipment, utilities, processes and controlled documents. To control this process, one must have both a defined change control procedure that outlines responsibilities and documentation requirements and also a form by which required information is recorded. The effectiveness of these items will determine the success of your change control program and help assure regulatory auditors that your equipment, utilities and systems remain in a state of control.
This seminar will concentrate on three major points:
- The regulatory requirements for change control and what it applies to.
- How to develop a change control SOP that will define what is required, responsibilities, and a means to quickly provide summaries of changes to investigators.
- What are some of the common deficiencies cited by regulatory auditors?
August 17, 2017 - August 18, 2017
DoubleTree by Hilton San Diego Downtown, San Diego, Ca
Phone: 800-447-9407
