MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Expectations of Regulatory & Validation Master Planning - 2017

Event Details

Expectations of Regulatory & Validation Master Planning - 2017

Time: July 20, 2017 from 10am to 11am
Location: Online
Street: 161 Mission Falls Lane, Suite 216,
City/Town: Fremont
Website or Map: http://www.compliance4all.com…
Phone: 18004479407
Event Type: webinar
Organized By: Netzealous LLC DBA - Compliance4All
Latest Activity: May 26

Export to Outlook or iCal (.ics)

Event Description

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@compliance4All.com

Comment Wall

Comment

RSVP for Expectations of Regulatory & Validation Master Planning - 2017 to add comments!

Join MedTech I.Q.

Attending (1)

© 2017   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service