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What does GLP stands for?

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Anonymous

13y ago
Updated: 8/20/2019

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What is GLP in Pharma industry?

<p><p> "Good Laboratory Practice" GLP practicing methods, Procedures according to the Stated Standards. The standards could of ICH guidlines, ISO etc. Arshad Anjum. ArshadAnjum5@yahoo.com Arshadanjum5@gmail.com


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GLP what is a note to file?

A "note to file" in Good Laboratory Practice (GLP) is a document used to clarify or provide additional information regarding specific aspects of a study or experiment. It serves to ensure transparency and traceability, addressing any deviations or issues that may arise during the study that are not fully documented in the official study report. This note helps maintain compliance with regulatory standards by capturing important details that may affect the interpretation of the study results.


Which feedback mechanism is used to regulate blood glucose?

Negative feedback systems are processes that sense changes in the body and activate mechanisms that reverse the changes in order to restore conditions to their normal levels.Glucose levels are regulated by hormones including insulin, glucagon, amylin, GLP-1, glucose-dependent insulinotropic peptide (GIP), epinephrine, cortisol, and growth hormone. Of these, insulin and amylin are derived from the beta-cells, glucagon from the alpha-cells of the pancreas, and GLP-1 and GIP from the L-cells of the intestine.


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kogvfik gopdfkg o[ffg p[opg glp pf pporgpoh pop go[o. Hope that helps <|:P


What is good laboratory practice?

Good Laboratory Practice (GLP) is a set of principles aimed at ensuring the quality and integrity of non-clinical laboratory studies, primarily in the pharmaceutical, chemical, and agrochemical industries. It involves systematic planning, conduct, monitoring, and reporting of research to ensure reliability and reproducibility of results. GLP emphasizes proper documentation, training, and compliance with regulatory standards to safeguard public health and the environment. Ultimately, it helps to ensure that data generated from laboratory studies are trustworthy and can be used in regulatory submissions.


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