Good laboratory practice (GLP) regulations became effective in 1979 under 21 CFR Part 58 and apply to all non-clinical safety studies intended to support research permits or marketing authorizations.

Good Laboratory Practice (GLP): is a set of principles intended to assure the quality and integrity of non-clinical laboratory studies that are intended to support research or marketing permits for ...

Good Laboratory Practice (GLP): is a set of principles intended to assure the quality and integrity of non-clinical laboratory studies that are intended to support research or marketing permits for ...

Many of the GMP regulations and guidances apply to control laboratories but in particular Chapter 6 (QC and Good Control Laboratory Practice) of the EU Guide to GMP. The course also covers the role of ...

On August 24, 2016, the US Food and Drug Administration (FDA) issued a Proposed Rule on Good Laboratory Practice for Nonclinical Laboratory Studies... On August 24, 2016, ...

The Good Laboratory Practice Regulations (GLPs), developed in the late 1970s, were necessary because some of the research studies submitted to the US Food and Drug Administration (FDA) were poorly ...

Ultimately, compliance with GLPs depends on following best practices. Stuart Jones, regulatory quality assurance professional in good laboratory practice (RQAP-GLP) and director of quality assurance ...

Why good pipetting practices matter Along with computers, pipettes can often be the most common equipment type used in the laboratory. On average, personnel spend two hours a day pipetting, which ...

The pipette is arguably the tool that gives the scientist the most hands-on contact with their work. Though small, this simple piece of equipment can have a big impact on good laboratory practice (GLP ...