ComplianceOnline

Leadership in Manufacturing Contamination Control: The Microbiology Lab

Instructor: T.C Soli
Product ID: 701478
  • 13
  • February 2018
    Tuesday
  • 10:00 AM PST | 01:00 PM EST
    Duration: 60 Min

Live Online Training
February 13, Tuesday 10:00 AM PST | 01:00 PM EST | Duration: 60 Min

$199.00
One Dial-in One Attendee
$529.00
Group-Max. 10 Attendees/Location
(For Multiple Locations Contact Customer Care)
Super Deal - Get CD/USB Drive Free!

recorded version

$249.00
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 48 hrs after completion of Live training

Training CD / USB Drive

$349.00
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 after completion of Live training

Combo Offers

Live + Recorded Version

$349.00

Live + Training CD/USB

$449.00

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This webinar on Contamination Control will discuss, how the micro lab can be more effectively utilized to prevent or head off microbial contamination issues as well as effectively resolve problems like recurring micro failures, investigations, and ineffective CAPAs.

Why Should You Attend:

The Microbiology Lab must take leadership in contamination control support for production because it is the hub of the necessary technical expertise. This broad manufacturing support role covers many areas, including routine raw material and product testing, disinfectant/sanitant qualification, water and compressed gas testing, environmental monitoring, microbiological “awareness training” of production operators, etc. Perhaps their most difficult leadership role is in contamination control investigations where product is at risk, manufacturing may be at a standstill, and the pressure to resume operation with a quick (and possibly incorrect) fix is tremendous. In these situations, the microbiology lab can either gain or lose credibility in the eyes of manufacturing management depending on the timeliness of its success in discovering and resolving the problems.

This presentation will discuss these roles and how the lab can assure these activities are performed in a manner that facilitates root cause excursion investigations and avoids the lab or its personnel becoming the inadvertent cause of the excursions.

Areas Covered in the Seminar:

  • Why the microbiology lab must lead in contamination control.
    • Lab personnel have microbiological knowledge and expertise; QA usually doesn't
    • Lab uses tools and techniques able to assess contamination and sources
    • Lab uses appropriate controls to detect and prevent testing problems
  • Routine contamination evaluation activities.
    • RM and Product testing
    • Environmental monitoring
    • Water, steam, and compressed gas monitoring
    • Sanitizer and disinfectant evaluations
  • Microbiological awareness/aseptic process training for operators.
  • Root cause microbial contamination investigations.
    • Ability to interpret investigation data and microbial impact
    • Ability to withstand production pressure for hasty, potentially faulty conclusions
    • Truly understand cause(s) of problem so can derive effective CAPA
  • Microbiological conscience for the company

Who Will Benefit:

This webinar will be valuable for all companies that operate WFI or Purified Water systems, particularly for those in FDA and EMEA regulated industries, including Medical Devices, Diagnostics, Pharmaceuticals, and Biologics fields, as well as consumer products and cosmetics companies. The employees who will benefit include:

  • QA managers and personnel involved in investigations of excursions and preparing CAPAs
  • QC managers and personnel involved in sampling, testing, and trending chem and micro data from water systems
  • Utility operators and their managers involved in maintaining and sanitizing water systems
  • Validation managers and personnel
  • QA managers and Regulatory Affairs personnel involved in defending water system operations and quality data to FDA and EMEA inspectors and outside auditors
  • Consultants and Troubleshooters
Instructor Profile:
T.C Soli

T.C Soli
President, Soli Pharma Solutions, Inc.

Dr. Teri C. ("T.C.") Soli ,Ph.D. is President of Soli Pharma Solutions, Inc. (www.solipharmasol.com), and has been consulting full time for 5 years, serving consumer products and FDA-regulated industries with training and troubleshooting expertise covering water systems, sterilization, aseptic processing, microbiological and beta-lactam contamination control, and microbiological laboratory operations. Prior to consulting, he had 25 years of diverse "Big Pharma" operating company experience.

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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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