2017 - Expectations of Regulatory & Validation Master Planning - 2017

Overview:
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
Types
Organization
Requirements
Regulatory expectations
Maintenance
Who Will Benefit:
Compliance Personnel
QA Personnel
validation Personnel
Speaker Profile:
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.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com