ComplianceOnline

How to Choose a Quality Management System for FDA-regulated Environment

Instructor: Anil Gupta
Product ID: 700077
Training Level: Basic To Intermediate
  • Duration: 60 Min

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD / USB Drive

$500.00
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

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This Quality Management System training will discuss how to choose an advanced and comprehensive system for quality and compliance management to meet the unique needs of the FDA-regulated environment.

Description

Many Pharmaceutical, Biotech, and Medical Device companies are finding that home grown or spreadsheet-based Quality Management System have become an impediment to their growth.

Insights for quality and compliance managers looking to replacing their point solutions and paper-based systems with an enterprise solution to automate key compliance processes including document control, deviations handling, and CAPA management.

Such systems come apart at their seams as companies grow, resulting in a high risk of non-compliance with cGMP and 21 CFR Part 11 regulations.

Areas Covered in the Webinar:

In this Webinar, the presenter will discuss how to choose an advanced and comprehensive system for quality and compliance management to meet the unique needs of the FDA-regulated environment.

It will provide insights to quality and compliance managers looking to replacing their point solutions and paper-based systems with an enterprise solution to

  • Automate the quality management processes
  • Gain real-time visibility into the quality metrics
  • Lower their cost of regulatory compliance
  • Reduce the risk of non-compliance.

The Webinar will cover automation requirements of key compliance processes including document control, deviations handling, and CAPA management.

Who Will Benefit:

  • Quality managers
  • Compliance managers
  • Regulatory professionals
  • Documentation department personnel
  • Quality System professionals
  • Quality Analyst & executives
  • Technical Quality Auditor
  • Quality Control / Assurance - Controller

Instructor Profile:

Anil Gupta, is the Principal of The Applications Marketing Group. He brings over 20 years of experience in marketing enterprise applications, with over half of that in manufacturing and supply chain management. Anil has also consulted with various software and manufacturing companies on planning, materials management, quality management and compliance related issues. Anil has also served as VP of Product Strategy at software companies such as Baan and Niku.

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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. ComplianceOnline 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@complianceonline.com call +1-888-717-2436 (Toll Free).

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