May 25, 2019   SOURCE: BusinessWire

Virtual Seminar on Good Laboratory Practices (GLPs) Comparing and Contrasting GMP - ResearchAndMarkets.com

The "6-Hour Virtual Seminar on Good Laboratory Practices (GLPs) Comparing and Contrasting GMP" webinar has been added to ResearchAndMarkets.com's offering.

The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.

Why you should attend

Good Laboratory Practices (GLPs), 21 CFR part 58, are a set of guidelines for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA.

GLPs are enforceable by law. They do not include manufacturing of product. GLPS are for non-clinical laboratory studies in which tests article are studied in test system under laboratory conditions to determine their safety. This does not include studies utilizing human subjects, or clinical studies, or field trials on animals.

Attendees:

  • Quality Assurance Personnel
  • Quality Control Personnel
  • Research and Development Personnel
  • Regulatory Affairs Personnel
  • Project Managers
  • Manufacturing Managers
  • Validation Engineers
  • Internal Auditing Personnel
  • Microbiology Personnel
  • Auditors

Agenda

  • GLP: Good Laboratory Practice
  • GLP is an FDA Regulation
  • Definition of GLPs
  • History of GLPs
  • Why was GLP Created?
  • Objectives of GLP
  • Mission of GLP
  • Instrumentation Validation
  • Analyst Certification
  • Laboratory Certification
  • Grounds for Disqualification
  • Consequences of Noncompliance
  • Reinstatement of a Disqualified Facility
  • References

For more information about this webinar visit https://www.researchandmarkets.com/r/b2pypg