This presentation will cover the importance of master planning. The FDA and other regulatory bodies expect these to be among the Quality System documentation.
Areas Covered in the Session:
History and background
Who Will Benefit:
Louis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of experience in Quality Assurance, Quality Control, Validation, consent decree remediation as well as cGMP Compliance in the Medical Device and Pharmaceutical industries.
Compliance4All DBA NetZealous,
Full Details & Registration Link: http://www.compliance4all.com/control/w_product/~product_id=501357LIVE?channel=ticketprinting_Jul_2017_SEO