How to Implement a GLP Quality Management System

  • William D Fox
  • 24, April 2019 Wednesday
  • 10:00 AM PDT | 01:00 PM EDT (90 Min)

This GLP quality system webinar provides a general overview of the Proposed Rule, a GLP QMS and its implementation, GAP analysis, Plan-Do-Check-Act cycle, process control and optimization theory and quality audits are utilized for the analysis of an existing QMS and the potential benefits, barriers steps to implementing an optimized GLP QMS.

Live Online Training
April 24, Wednesday 10:00 AM PDT | 01:00 PM EDT (90 Min)

$249.00
One Dial-in One Attendee
$629.00
Group-Max. 10 Attendees/Location
(For multiple locations contact Customer Care)

Recorded Version

$299.00
1x Person - Unlimited viewing for 6 Months (For multiple locations contact Customer Care)
rec Recorded Link and Ref. material will be available in My Account Section 48 hrs after completion of Live training

Training CD / USB Drive

$399.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days after completion of Live training
Customer Care

Fax: +1-650-362-2367

Email: customercare@fdatrainingalert.com

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Areas Covered in the Webinar:
  • GLP Regulations
  • Quality Management System (QMS)
    • Definition
    • Principles
    • Purpose
    • Function
    • Elements
  • Quality Policy
  • Quality Objectives
  • Quality Manual
  • GLP SOPs
  • Plan, Do, Check, Act Cycle
  • GAP Analysis
  • QMS Implementation Steps
  • Process Control and Optimization Theory
  • Process Criteria
  • Quality Audit
Free Materials:
  • Proposed Rule Summary
  • Cost of QMS
  • GLP QMS GAP Analysis Checklist
  • Sample GLP QMS Table of Contents
  • Example of Process Flow & Criteria
  • Required GLP SOPs
  • SOP Template
  • Seven Tools of Quality Management
  • Terms: Define & Differentiate
Who Will Benefit:
  • Senior Managers, Managers & Supervisors
  • Process Owners
  • Departmental Heads
  • Quality System, QA, QC and Continuous Improvement Managers and Personnel
  • Quality Consultants
  • Regulatory and Compliance Managers
  • Change Control/Documentation Staff
Instructor Profile:
William D Fox William D Fox

Quality Management Professional, Texas Biomedical Research Institute

William D Fox is a quality management professional with a background in clinical research and quality assurance. William’s experience includes scientific, administrative, and quality aspects of regulated (ISO, GCP, GLP, GMP) pharmaceutical development and manufacturing and spans the translational interface (T1; late preclinical, early clinical) with a focus on oncology drug development and emerging disease vaccine development in BSL 2, 3 & 4 environments. William also has experience developing quality management systems, documents and change control systems in GLP, GCP and GMP settings.

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. FDATrainingAlert would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@fdatrainingalert.com call +1-888-771-6965 (Toll Free).

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