ComplianceOnline

Laboratory Quality and Safety Regulatory Compliance Training - Live Webinars, Recordings & CDs

Recorded/CD
Laboratory Accreditation: Getting there is Just the Beginning

Laboratory Accreditation: Getting there is Just the Beginning

  • Speaker: Michael Brodsky
  • Product ID: 703285
  • Duration: 60 Min
This training on laboratory accreditation will focus on ISO/IEC 17025 requirements. Attendees will learn how to develop and maintain a quality management system to ensure compliance with the international laboratory accreditation standard.
CD/Recorded
$249
Recorded/CD
Eliminate the Confusion - Analytical Method Qualification and Validation

Eliminate the Confusion - Analytical Method Qualification and Validation

  • Speaker: Melissa Smith
  • Product ID: 702314
  • Duration: 60 Min
This webinar will help you understand the significant differences between qualification and validation of an analytical method, the expectations and requirements of each, and their place in the analytical method lifecycle.
CD/Recorded
$229
Recorded/CD
Proficiency Testing: How to Pass with Flying Colors and What to Do If You Don't

Proficiency Testing: How to Pass with Flying Colors and What to Do If You Don't

  • Speaker: Barry Craig
  • Product ID: 701419
  • Duration: 60 Min
This Proficiency testing (PT) training/webinar for CLIA will explain the rules of PT testing, the PT testing "danger zones", and CLIA's stance on PT referral and also gives tips and techniques to assure good PT performance.
CD/Recorded
$299
Recorded/CD
Importance of Method Validation Protocols and components of MVP in the Laboratory

Importance of Method Validation Protocols and components of MVP in the Laboratory

  • Speaker: Brian Jones
  • Product ID: 701689
  • Duration: 27 Min
Learn method validation protocol components and how to include MVPs in your lab performance testing.
CD/Recorded
$249
Recorded/CD
Handling OOS Test Results and Failure Investigations

Handling OOS Test Results and Failure Investigations

  • Speaker: Dr. Ludwig Huber
  • Product ID: 701526
  • Duration: 75 Min
This OOS Webinar training will discuss how to handle OOS situations, requirements of ICHQ7A for APIs and how to develop CAPA plans, how to use checklists and forms and how to develop FDA compliant OOS documentation.
CD/Recorded
$399
Recorded/CD
Best Practices in GLP Final Reporting and Study Closure

Best Practices in GLP Final Reporting and Study Closure

  • Speaker: Anne E Maczulak
  • Product ID: 701091
  • Duration: 60 Min
This GLP (Good Laboratory Practices) webinar reviews the process of closing a study by preparing a final report and managing all records and specimens in a proper manner.
CD/Recorded
$299
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