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Good Laboratory Practices
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FDA Regulations

Pooja Govil
Delhi University Gold Medalist 💫 6 yrs teaching experience 😇 "Life is all about Learning and Laughing" 😄😄 Lets do it together.. 😎😎😎

U
Unacademy user
sir would you like to give us the book list of mains paper?
Pooja Govil
a year ago
welcome.. 😄😄😄
  1. GOOD LABORATORY PRACTICES BY: POOJA GOVIL


  2. WHATWE WILL STUDY? o Introduction o Objective of GLP o Mission of GLP


  3. INTRODUCTION GLP is an FDA regulation. Definition: GLP embodies a set of principles that provides a framework within which laboratory studies are planned performed, monitored, reported and archived. GLP is a formal regulation that was created by the FDA (United states food and drug administration) in 1978.


  4. OBJECTIVE OF GLP GLP makes sure that the data submitted are a true reflection of the results that are obtained during the study. GLP also makes sure that data is traceable. Promotes international acceptance of tests.


  5. MISSION OF GLP o Test systems 0 Archiving of records and materials. o Apparatus, material and reagent facilities. o Quality assurance programs o Performance of the study. o Reporting of study results. o Standard operating procedures (SOP) o Personnel and test facility organization


  6. REQUEST o Post any of your queries in the comment section below. o Don't forget to rate, review and recommend this video. 3 o Follow me on Unacademy https://unacademy.com/user/pooja.govil.09



  7. THANKYOU