Good Laboratory Practice — the Why and the How [electronic resource] / by Jürg P. Seiler.

Seiler, Jürg P.
Call Number
615
Author
Seiler, Jürg P. author.
Title
Good Laboratory Practice — the Why and the How by Jürg P. Seiler.
Physical Description
XII, 424 p. online resource.
Contents
What is Good Laboratory Practice All About? -- How is Good Laboratory Practice Regulated? -- How can Good Laboratory Practice be Introduced in a Test Facility? -- How is Compliance with Good Laboratory Practice Monitored?.
Summary
After more than twenty years of use Good Laboratory Practice, or GLP, has attained a secure place in the world of testing chemicals and other “test items” with regard to their safety for humans and the environment. Gone are the days when the GLP regulations were hotly debated amongst scientists in academia and industry and were accused of stifling flexibility in, imaginative approaches to, and science-based conduct of, all kinds of studies concerned with toxic effects and other parameters important for the evaluation and assessment of products submitted for registration and permission to market. The GLP regulations have developed from rules on how to exactly document the planning, conduct and reporting of toxicity studies to a quality system for the management of a multitude of study types, from the simple determination of a physical/chemical parameter to the most complex field studies or ecotoxicology studies. At the same time the term “Good Laboratory Practice” has become somewhat of a slogan with the aim to characterise any reliably conducted laboratory work.
Added Author
SpringerLink (Online service)
Subject
MEDICINE.
PHARMACY.
SCIENCE.
MOLECULAR BIOLOGY.
PHARMACOLOGY.
BIOMEDICAL ENGINEERING.
Biomedicine.
Pharmacology/Toxicology.
Science, general.
Biomedical Engineering.
Molecular Medicine.
Pharmacy.
Medicine/Public Health, general.
Multimedia
  • Libraries with this item
Total Ratings: 0
No records found to display.
 
 
 
02980nam a22005415i 4500
001
 
 
vtls001568751
003
 
 
VRT
005
 
 
20170831184800.0
007
 
 
cr nn 008mamaa
008
 
 
170831s2005    gw |    s    |||| 0|eng d
020
$a 9783540282341 $9 978-3-540-28234-1
024
7
$a 10.1007/3-540-28234-3 $2 doi
035
$a (DE-He213)978-3-540-28234-1
039
9
$y 201708311848 $z santha
050
4
$a RM1-950
072
7
$a MMG $2 bicssc
072
7
$a MED071000 $2 bisacsh
082
0
4
$a 615 $2 23
100
1
$a Seiler, Jürg P. $e author.
245
1
0
$a Good Laboratory Practice — the Why and the How $h [electronic resource] / $c by Jürg P. Seiler.
264
1
$a Berlin, Heidelberg : $b Springer Berlin Heidelberg, $c 2005.
300
$a XII, 424 p. $b online resource.
336
$a text $b txt $2 rdacontent
337
$a computer $b c $2 rdamedia
338
$a online resource $b cr $2 rdacarrier
347
$a text file $b PDF $2 rda
505
0
$a What is Good Laboratory Practice All About? -- How is Good Laboratory Practice Regulated? -- How can Good Laboratory Practice be Introduced in a Test Facility? -- How is Compliance with Good Laboratory Practice Monitored?.
520
$a After more than twenty years of use Good Laboratory Practice, or GLP, has attained a secure place in the world of testing chemicals and other “test items” with regard to their safety for humans and the environment. Gone are the days when the GLP regulations were hotly debated amongst scientists in academia and industry and were accused of stifling flexibility in, imaginative approaches to, and science-based conduct of, all kinds of studies concerned with toxic effects and other parameters important for the evaluation and assessment of products submitted for registration and permission to market. The GLP regulations have developed from rules on how to exactly document the planning, conduct and reporting of toxicity studies to a quality system for the management of a multitude of study types, from the simple determination of a physical/chemical parameter to the most complex field studies or ecotoxicology studies. At the same time the term “Good Laboratory Practice” has become somewhat of a slogan with the aim to characterise any reliably conducted laboratory work.
650
0
$a MEDICINE.
650
0
$a PHARMACY.
650
0
$a SCIENCE.
650
0
$a MOLECULAR BIOLOGY.
650
0
$a PHARMACOLOGY.
650
0
$a BIOMEDICAL ENGINEERING.
650
1
4
$a Biomedicine.
650
2
4
$a Pharmacology/Toxicology.
650
2
4
$a Science, general.
650
2
4
$a Biomedical Engineering.
650
2
4
$a Molecular Medicine.
650
2
4
$a Pharmacy.
650
2
4
$a Medicine/Public Health, general.
710
2
$a SpringerLink (Online service)
773
0
$t Springer eBooks
776
0
8
$i Printed edition: $z 9783540253488
856
4
0
$u http://dx.doi.org/10.1007/3-540-28234-3
912
$a ZDB-2-SBL
950
$a Biomedical and Life Sciences (Springer-11642)
999
$a VIRTUA               
No Reviews to Display
Summary
After more than twenty years of use Good Laboratory Practice, or GLP, has attained a secure place in the world of testing chemicals and other “test items” with regard to their safety for humans and the environment. Gone are the days when the GLP regulations were hotly debated amongst scientists in academia and industry and were accused of stifling flexibility in, imaginative approaches to, and science-based conduct of, all kinds of studies concerned with toxic effects and other parameters important for the evaluation and assessment of products submitted for registration and permission to market. The GLP regulations have developed from rules on how to exactly document the planning, conduct and reporting of toxicity studies to a quality system for the management of a multitude of study types, from the simple determination of a physical/chemical parameter to the most complex field studies or ecotoxicology studies. At the same time the term “Good Laboratory Practice” has become somewhat of a slogan with the aim to characterise any reliably conducted laboratory work.
Contents
What is Good Laboratory Practice All About? -- How is Good Laboratory Practice Regulated? -- How can Good Laboratory Practice be Introduced in a Test Facility? -- How is Compliance with Good Laboratory Practice Monitored?.
Subject
MEDICINE.
PHARMACY.
SCIENCE.
MOLECULAR BIOLOGY.
PHARMACOLOGY.
BIOMEDICAL ENGINEERING.
Biomedicine.
Pharmacology/Toxicology.
Science, general.
Biomedical Engineering.
Molecular Medicine.
Pharmacy.
Medicine/Public Health, general.
Multimedia