Microbiological cGMP Requirements for the Non-Sterile and Aseptic Fill ‘n Finish Environment

Live, Interactive Training Webinar

Date: Thursday July 11, 2019 - Time: 10:30 AM - 12:30 PM (Eastern New York Time)
Instructor: Barry Friedman Ph.D. Biography>>>

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As a product proceeds through manufacturing to the API with the addition of various excipients, both non-sterile and sterile products (aseptic fill ‘n finish) must be tested for their microbiological content. With non-sterile products, a limited number of microorganisms are acceptable; with sterile products, no microorganisms may be present. Often issues of OOT, OOS and CAPAs become critical at this juncture point. Quality Metrics and their Risk Based implications of deviation related issues will be considered for both non-sterile and aseptically produced products.

The objective of this live training webinar is to obtain an enhanced understanding as well as a “refresher” of what requirements exist for the microbiologist from the end of production through final release for both non-sterile and aseptic produced products. A review of Case Studies/Warning Letters pertinent to all phases of the microbiological release (microbiologist’s environment) will be reviewed to enhance the learning benefits.

Learning Benefits:
- Gain an overall review of cGMP and those sections of 21 CFR 211 that impact microbiology within a fill ‘n finish environment
- Review non-sterile products and how USP<61>, <62>, and <1115> impact these products and the number of microorganisms and species permitted in final products
- Review aseptically produced products and how the revised USP<1116> may impact any observed contamination within the Clean Room environment
- Study how OOT, OOS and CAPAs impact all aspects of the microbiological environment
- Review the use of metrics and risk management to assess problem solutions
- Case studies to include Form FDA 483s and Warning Letters

Webinar outline and time breakdown:

Time*
10:15 AM Log In Period
10:30 AM Introduction
10:40 AM Definitions,
Considerations of USP <61>, <62> and <1115>,
Issues with Non-Sterile Product in a Fill ‘n Finish Environment,
Number and Species of Microorganisms Permitted in Non-Sterile Products,
Issues with Sterile Products in a Fill ‘n Finish Environment,
Gaining an Understanding of USP Sterility Tests <71> and the Impact of a Positive Result,
A Review of the Revised USP <1116>
11:30 AM Break
1a:40 AM Deviations, Out of Specifications and Out of Trend and Their Impact on The Final Product,
The Use of Metrics to Assess Problem Solutions,
Frequency of 21 CFR 211 Microbiological Observations Within Final Products
Case Studies to Include Form FDA 483s and Warning Letters,
12:30 PM Live Questions & Discussion

*Please note all times are Eastern Time (New York Time)

This live training webinar includes the following for each registered attendee:

  • A copy of the presentation slides
  • A certificate of training for attendee records

Who should attend:
The following individuals or disciplines will benefit from attending this Webinar:

  • Quality Assurance personnel
  • Quality Control personnel
  • Research & Development
  • Microbiology Personel
  • Regulatory Affairs Professionals
  • Project Managers/li>
  • Those that use contract manufacturing and contract testing facilities

Registration Form ►


Instructor: Barry A. Friedman Ph.D.

Barry A. Friedman, Ph.D., is a Senior Consultant in the Biotechnology, Regulatory Compliance and Aseptic Processing arena. Dr. Friedman is a frequent seminar speaker in the GMP areas of internal auditing, aseptic processing of sterile drug products, USP microbiology, validations and the requirements for the manufacture of Phase 1, 2 and 3 clinical trial materials. He has recently given presentations for the FDA, PDA, PTi. He is a member of AAMI, ASM, PDA and RAPS. He served as a Captain in the Medical Service Corps, U.S. Army and is the past President of the Capital Area Chapter, PDA... Full Bio>>>

 

 

Course Number: 247

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Client Testimonials:

"The live webinar was very useful to our team, the content was relevant and the instructor was very knowledgeable" QC Microbiology Supervisor, NJ

"We were very satisfied with the live presentation; we appreciated the speaker staying on to answer all of our questions" QA Director, MA

"Our group enjoyed the live presentation and found the experience much more engaging and worthwhile than any recorded webcasts" Sr Training Manager, CA

"This was my first live training, I found it easy to connect, participate and very useful" Laboratory Analyst, PA

"We had our entire department attend this training program and found it to be very useful, I am very satisfied with the speaker's ability to keep the audience engaged" QC Manager, NY

"Given how recent the content of the webinar was, our team members were very happy with the relevance of the training" VP Clinical Operations, CA

"Is my first time to attend training, I enjoy it very much" Sr Manager, Korea

"Our department found the level of interactivity between the audience and the instructor far beyond that of any other online training that we have attended before. Well done" Director Regulatory Affairs, ON

"Our interest group was spread out over three locations and we were able to participate simultaneously and interact very easily" Lead Compliance Manager, IL

"Well satisfied with the presentation. Our team found the speaker's level of knowledge and his ability to translate that knowledge to our processes very valuable" VP Quality Operations, NC

"We were impressed with the quality of the presentation, and despite our being located in Europe we were able to participate without a hitch" QC Manager, Ireland