Validation Sampling Plans, Setting Acceptance Specifications, and Statistical Process Control

Alan M Golden 
Instructor: Alan M Golden 
Date: Thursday November 21, 2024
Time:

10:00 AM PST | 01:00 PM EST

Duration: 60 Minutes
Webinar Id: 23470

Price Details

Live Webinar
$150. One Attendee
$290. Unlimited Attendees
Recorded Webinar
$190. One Attendee
$390. Unlimited Attendees
Combo Offers   (Live + Recorded)
$289 $340   One Attendee
$599 $680   Unlimited Attendees

Unlimited Attendees: Any number of participants

Recorded Version: Unlimited viewing for 6 months (Access information will be emailed 24 hours after the completion of live webinar)

Overview:

Setting up an appropriate sampling plan for process and setting appropriate acceptance criteria is critical for successful validation activities.

Regulatory agencies expect statistically justified sampling plans as well as statistically justified acceptance criteria. In this presentation, we will discuss a 5 step approach to setting up sampling plans, and using those sampling plans to set appropriate acceptance criteria for process validations. We will discuss a risk-based approach to determine sampling and confidence levels needed depending on the validation and risk of release of non-conforming product. 

After a process is validated, it is important to ensure it is maintained in a validated state. We will discuss the tools available using statistical process controls to provide continual monitoring of the process to ensure that is continues to perform as validated and to be able to take proactive measures if the date shows adverse trending. 

Why you should Attend:

This webinar will be useful to validation engineers, R&D scientists, quality professionals and production personnel involved in validation activities. Validation professionals in both medical device and pharmaceutical industries will benefit. Setting up sampling plans is a joint effort between the above team members who each bring a part to the table. An understanding of how to set up appropriate sampling plans and setting appropriate acceptance criteria is critical to a successful validation. 

I don't do FUD.

Areas Covered in the Session:

  • What is sampling
  • Validation sampling vs lot acceptance sampling
  • Setting up a validation sampling plan: 5 step method
  • Using sampling plans to set acceptance criteria for process validations
  • Use of process capability to set acceptance criteria
  • Statistical process control and maintaining a controlled state

Who Will Benefit:

  • Quality Assurance Professionals
  • R&D Scientists
  • Technical Support Scientists
  • Regulatory Affairs Professionals
  • Manufacturing and Production Personnel Involved in Validation Activities
  • Both Pharmaceutical and Medical device Professionals are Appropriate

Speaker Profile
Alan M Golden has over 35 years of experience in the medical device industry, both in basic research and in quality assurance. Alan spent 31 years at Abbott Laboratories. For the first 16 years as part of diagnostics R&D, he developed recombinant proteins used in diagnostics tests, received three US patents and published numerous papers and abstracts. Alan then transitioned to a quality assurance role where in both the Abbott Diagnostics and Abbott Molecular divisions, he was responsible for quality assurance for new product development, on-market product support and operations.

Alan’s quality assurance experience extends from design control, change control, risk management, CAPA, process and test method validation and statistics. He has been lecturing on these topics worldwide for over 20 years.

Alan retired from Abbott in 2018 and now runs Design Quality Consultants, providing training, workshops and seminars in many areas of quality assurance.

Alan received his BS degree in Microbiology from the University of Michigan and his MS degree in Molecular Biology and Immunochemistry from the University of Illinois.

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