Comparing and Contrasting Good Laboratory Practices (GLPs) with GMPs

Event Information
Product Format
Prerecorded Event
Presenter(s)
Conference Date
Fri, Aug 25, 2017
Length
90 minutes
Product Description

How Good Laboratory Practices Associate with Good Manufacturing Practices


According to the FDA, CFR part 58, good laboratory practices (GLPs) 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.

As per the FDA, GLPS are for non-clinical laboratory studies in which test articles 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. GLPs are not enforceable by law. They do not include the manufacturing of the product. However, it is important to be able to compare and contrast GLPs with GMPs and understand their requirements.

Join this session, where expert speaker Joy McElroy will compare and contrast between good laboratory practices (GLPs) and good manufacturing practices (GMPs). She will discuss the objective behind GLPs and how they associate with GMPs and SOPs, and the consequences of non-compliance.

Session Objectives

  • What are good laboratory practices (GLP)?
    • GLP is an FDA regulation
    • Definition of GLPs
    • History of GLPs
    • Why were GLPs created?
    • Objectives of GLPs
    • Mission of GLPs
  • The objective of GLPs and how are they associated with GMPs and SOPs
  • Statistical procedures for data evaluation
  • Instrumentation validation
  • Analytical and laboratory certification
  • Documentation and maintenance of records
  • Consequences of noncompliance
  • Grounds for disqualification
  • Reinstatement of a disqualified facility
  • References

Who Should Attend

  • 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

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.

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About Our Speaker

Joy McElroy

Joy McElroy made her debut in the pharmaceutical industry in 1992 at Pharmacia & Upjohn performing environmental monitoring and sterility testing after earning a degree in zoology at North Carolina State University. She moved into a supervisory role at Abbott Laboratories where she oversaw their Quality Control Lab.  In 1998 Joy moved to Wyeth Lederle and worked in Quality Assurance, performing GMP Compliance audits, batch record reviews, and...   More Info
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