ComplianceOnline

Laboratory Quality and Safety Regulations Training, Compliance Best Practices and Standards

Laboratory quality and safety regulation based webinars, in-person seminars, standards and best practices. Learn from renowned experts about FDA regulations for quality and safety in laboratories - USP chapter <1226>, USP chapter <1224>, USP <1058>, Method Validation Protocols (MVP), etc.
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
$199
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
$149
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. The GLP final study report represents the last chance for a study team to present their results in a clear and compelling manner. The report may also be a place where difficulties can be explained so that the study provides meaningful and trustworthy information. This webinar reviews the process of closing a study by preparing a final report and managing all records and specimens in a proper manner. It provides two areas of concentration: (1) the best practices in final report writing and (2) the step-by-step process of closing studies.
CD/Recorded
$299
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