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Penanda Bagikan

E Book

Good Laboratory Practice

Seiler, Jürg P. - Nama Orang;

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?.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.


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Informasi Detail
Judul Seri
-
No. Panggil
-
Penerbit
Berlin, Heidelberg : Springer., 2005
Deskripsi Fisik
XII, 424 p.online resource.
Bahasa
English
ISBN/ISSN
9783540282341
Klasifikasi
615
Tipe Isi
-
Tipe Media
-
Tipe Pembawa
-
Edisi
2nd ed.
Subjek
Biomedical engineering.
Biomedical Engineering and Bioengineering.
Medicine.
Medicine/Public Health, general.
Pharmacology.
Pharmacology/Toxicology.
Science, Humanities and Social Sciences, multidisciplinary.
Molecular biology.
Molecular Medicine.
Pharmacy.
Info Detail Spesifik
-
Pernyataan Tanggungjawab
Jürg P. Seiler.
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UPT Perpustakaan UNS
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