What is GMP, GLP?????????
Answers were Sorted based on User's Feedback
Answer / p
Good Manufacturing Practices, Good Laboratory Practices
| Is This Answer Correct ? | 29 Yes | 3 No |
Answer / anuj sharma
GMP:-"Good manufacturing practice" or "GMP" is part of a
quality system covering the manufacture and testing of
active pharmaceutical ingredients, diagnostics, foods,
pharmaceutical products, and medical devices. GMPs are
guidelines that outline the aspects of production and
testing that can impact the quality of a product.
GLP:-GLP generally refers to a system of management
controls for laboratories and research organizations to
ensure the consistency and reliability of results.
ANUJ SHARMA
IPQA, INDSWIFT LABS CHANDIGARH
| Is This Answer Correct ? | 24 Yes | 2 No |
Answer / satish
good manufaturing practices, good laboratory practicis
| Is This Answer Correct ? | 22 Yes | 5 No |
Answer / deepika singh, ipqa navdeep bi
Good Laboratory Practice (GLP) embodies a set of principles
that provides a framework within which laboratory studies
are planned, performed, monitored, recorded, reported and
archived. GLP helps assure regulatory authorities that the
data submitted are a true reflection of the results
obtained during the study and can therefore be relied upon
when making risk/safety assessments.
Good manufacturing practice- is a part of quality system
which ensures that products are consistently produced and
controlled to the quality standards appropriate to their
intended use and as required by the marketing authorization.
| Is This Answer Correct ? | 11 Yes | 0 No |
Answer / kishor raut
cGMP mean updating the system as per current regulation and guideline
GLP is planned, performed, monitored, recorded, reported and archived. GLP helps assure regulatory authorities that the data submitted are a true reflection of the results
obtained during the study ..
| Is This Answer Correct ? | 2 Yes | 0 No |
Answer / anil kumar
good manufacturing practice ,good laboratory practice
| Is This Answer Correct ? | 5 Yes | 4 No |
Answer / anil kumar
good manufacturing practice ,good laboratory practice
| Is This Answer Correct ? | 4 Yes | 3 No |
Answer / kaushlesh bahadur singh
GMP:-"Good manufacturing practice" or "GMP" is part of a
quality system covering the manufacture and testing of
active pharmaceutical ingredients, diagnostics, foods,
pharmaceutical products, and medical devices. GMPs are
guidelines that outline the aspects of production and
testing that can impact the quality of a product.
Good Laboratory Practice (GLP) embodies a set of principles
that provides a framework within which laboratory studies
are planned, performed, monitored, recorded, reported and
archived. GLP helps assure regulatory authorities that the
data submitted are a true reflection of the results
obtained during the study and can therefore be relied upon
when making risk/safety assessments.
| Is This Answer Correct ? | 2 Yes | 1 No |
Answer / alxender
GLP Good laboratories Practiecs which covers all the documentory, restrictions safety working style plane and data saving covers in GLP
| Is This Answer Correct ? | 0 Yes | 0 No |
GMP : It is an abbreviation of Good manufacturing practices. These practices are applicable when a drug manufactured for human being . This is a system by which it is ensure that the products are consistently manufactured and are controlled by quality standards.
GLP : It is an abbreviation of Good Laboratory practices and it is applicable for non-clinical research laboratories. 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 products regulated by government agencies.
| Is This Answer Correct ? | 0 Yes | 0 No |
who is the father of pharmacy?
What is the role of buffers in HPLC analysis
What is the role of buffers (ex: KH2PO4) in HPLC analysis,
what do you call "talking while sleeping at night" in english langusge?
Tell us about your oncology experience.
What do you mean by GTT? What are the effect of GTT on film coating.
Why 3 validation batches charge in stability ?is there any specific reason for 3 ?
related substances test replicate injection is allow or not if allow so rsd limit how many %?
what is the mechanism of action of local anaesthetics?
What r the different sop in or plant
Job oriented Training in Oracle Clinical, CDM, Clinical Research and SAS with Clinical Trails
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc?