ComplianceOnline

Quality System Development: Strength, Compliance and Efficiency through Value Stream Mapping

Instructor: Philip Russ
Product ID: 703490
  • Duration: 60 Min

recorded version

$229.00
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

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

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Read Frequently Asked Questions

This webinar will explain the principles of lean and value stream mapping. Attendees will learn how to apply lean concepts to continuous improvement work across the quality system.

Why Should You Attend:

Inefficient quality systems are costly and cumbersome to use. Your firm’s ability to be in compliance and have nimble, efficient business processes to support compliance is critical to the operational and financial success of your business. Applying the cost cutting and efficiency driving concepts of lean as it relates to quality systems will help you to make the best contribution to your firm’s long term success without sacrificing compliance and quality.

This webinar will present a practical approach to quality system continuous improvement through value stream mapping. This approach incorporates key value factors of compliance, cycle-time and user friendliness and techniques for enhancing the efficiency and usefulness of various quality systems. Value stream mapping based on the CAPA model will also be discussed during the webinar.

Learning Objectives:

  • Understand the value and the process development of a lean quality system.
  • Use value stream mapping tools for quality system development.
  • Incorporate the factors of compliance, user friendliness and cycle-time in the value stream model.
  • Apply the principles of lean to your continuous improvement work across the quality system, increasing efficiency and effectiveness within the barriers of regulatory compliance requirements.

Areas Covered in the Webinar:

  • Quality system problems
  • Key principles of lean and value stream mapping
  • How to apply lean concepts to quality systems
  • Meaningful quality system value ratio evaluation
  • CAPA model value stream mapping
  • Continuous improvement

Who Will Benefit:

  • Quality and Compliance Professionals
  • Quality Engineers
  • IT Professionals
  • Operations Personnel
  • R&D Personnel
  • Equipment, Facilities and Process Engineering Professionals

Instructor Profile:

Philip Russ, is an experienced quality/compliance professional with 20 years’ experience in the pharmaceutical, medical device and biologics industry. He has a record of success developing and managing quality systems to support these businesses. He has a breadth of experience performing/coordinating compliance audits involving CFR210/211, CFR820, ISO13485, QSR/PAL and CMDCAS regulations.

Mr. Russ has provided expert counsel in quality systems for early development projects; pioneering drug/medical device/drug combo quality systems and compliance initiatives; designing statistical and attribute analysis programs for manufacturing processes; continuous improvement, auditing, supplier quality management, technology transfer and validation support; statistical process controls; QA expertise for development activities, design controls and GCP for both medical device and drug products.

Mr. Russ is the owner and principal consultant of ICGXP. ICGXP offers a range of regulatory compliance and quality assurance services. Inspection readiness is an expertise that Mr. Russ and his team of associates provide clients to benefit their compliance profile and foster success in the market place.

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