Process Mapping for Risk-Based P&PC Using Lean Six Sigma and HACCP

Food & Beverages Pharmaceuticals

Date: 28 Jul '21
Time: 10:00am to 1:00pm (GMT-08:00) Pacific Time (US and Canada); Tijuana
CPD/CME/CEU: 95002

Visit Event Website

This webinar will discuss the basic principles of P&PC, specifically as required by the FDA. Also attendees will learn the ISO 13485 and risk analysis / management requirements to evaluate the chief areas of an FDA CGMP compliance inspection / audit to locate areas for implementation and improvement in P&PC.

Why Should You Attend:

There is an on-going major shift in the emphasis of U.S. FDA CGMP compliance emphasis. The 2011 Pharma Process Validation Guidance Document emphasizes “P&PC” to ensure “homogeneity within batch” and “consistency between batches”, basic Dr. Deming, et al. Such changes in regulatory focus should have a major impact on individual compliance objectives, efforts and measurements of success. Using P&PC, lean, six sigma / SPC, together with process mapping / flow charting and HACCP, will yield major business benefits as well: Reduced waste / scrap, early warning of process shifts before non-conforming product is manufactured, increase efficiencies, minimal need for re-validations of equipment and/or process, and opportunities for improvement in quality, through-put. A case of regulatory / business “win-win”.

P&PC systems, metrics, and information / analysis, combined lean principles, and six sigma / SPC tools, and the FDA’s QSIT for medical devices and pharmaceutical requirements, together provide an effective, proactive and aggressive / robust methodology to maintain a production process in a “state of statistical control”, and in CGMP compliance for any regulated industry. Software, data integrity, and cybersecurity issues are considered. Such a system greatly reduces the need for equipment / process re-verification / -qualification / -validation.

Areas Covered in the Webinar:

  • P&PC and U.S. FDA CGMP / ISO 13485 / 9001 requirements
  • Tougher FDA Expectations / Requirements
  • Key elements of P&PC in a regulated industrial environment
  • Process mapping / flow charting and P&PC
  • Lean manufacturing’s role
  • Basis easy to learn / teach / use six sigma / SPC tools
  • “Risk-based” per ISO 14971 / ICH Q9
  • Documentation
  • Prove / maintain “in statistical control”
  • Document – lot / batch records, logs, analysis / charts…

Who Will Benefit:

  • Senior and middle management.
  • Quality Assurance/ Quality Control
  • Regulatory Affairs
  • R&D
  • Engineering
  • Operations
  • Production / Manufacturing
  • Staff and Line personnel
  • Sales and Marketing





Copyright © 2021 Industry Events. All rights reserved. Site credit.