Compliance4alllearning
Knowledge. Creativity. Performance
  • Category
    • Medical Device (ISO 13485)
    • Drugs / Biologics
    • FDA Compliance
    • Food & Beverages
    • Quality Management (ISO 9001)
    • OSHA Compliance
    • IT Security
    • Sox Compliance
    • Clinical Compliance
    • Auditing/Accounting & Tax
    • Banking & Insurance
    • Geology and Mining
    • Risk Management
    • Project Management
    • Intellectual Property Law
    • Excel Spreadsheet Techniques
    • FAA Compliance
    • Trade & Logistics
    • Retail
    • Environmental Compliance
Cart 0
Sign In Sign Up Cart 0
  • Home
  • About Us
  • Live Webinars
  • Recorded Webinars
  • Webinar Pack
  • Products/E-Books
  • Toll free: +1-800-447-9407
  • 10 per page
  • 20 per page
  • 30 per page
  • View All
  • 10 per page
  • 20 per page
  • 30 per page
  • View All
Recorded Webinars
Jerry Lanese

Analytical Method Validation

An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Jerry Lanese

Laboratory Investigation of Out-of-Specification Results

The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Jerry Lanese

Analytical Method Validation

An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Jerry Lanese

Laboratory Investigation of Out-of-Specification Results

The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Jerry Lanese

Analytical Method Validation

An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Jerry Lanese

Laboratory Investigation of Out-of-Specification Results

The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Jerry Lanese

Laboratory Investigation of Out-of-Specification Results

The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Jerry Lanese

cGMPs in the Quality Control Laboratory

Since the mid 1980s, the Quality Control Lab oratory has been a prime target for FDA investigators during site inspections. Since that time, investigators have made many 483 observations. Unless the firm reacts very aggressively, the 483 observations will be escalated to Warning Letter citations.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤189.00 | View Details
Jerry Lanese

Analytical Method Validation

An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

Speaker: Jerry Lanese | View Anytime | Duration: 90 Minutes | Price: ¤189.00 | View Details
  • 10 per page
  • 20 per page
  • 30 per page
  • View All
  • 10 per page
  • 20 per page
  • 30 per page
  • View All
Compliance4alllearning
39658 Mission Boulevard, Fremont, CA 94539, USA.
+1-800-447-9407
Fax: 302 288 6884
support@compliance4alllearning.com

Links

About Us Contact Us Privacy Policy Refund Policy Terms & Conditions FAQ Support Featured Speakers Speaker Opportunity Suggest a Topic

Newsletter

Subscribe for Compliance Alerts Research Reports Absolutely Free

Safe & Secure


Safe & Secure

Copyright © 2025 compliance4alllearning. All rights reserved.