Jul 20, 2017 | 10:00 AM | Thursday
Our Speaker will explain the expectations of regulatory authorities both domestic and international.
Start on : July 20, 2017 10:00 AM Thursday
End on : July 20, 2017 11:00 AM Thursday
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,
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