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Recommendations for the evaluation of animal cell cultures ...
Historically, the major concerns regarding the safety of biological medicinal products manufactured in animal cells have been related to the possible presence of microbial contaminants and, in some cases, to the properties and components of the cells themselves such as DNA and proteins.
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INVESTING IN HEALTH FOR ECONOMIC …
www.who.int2 INVESTING IN HEALTH FOR ECONOMIC DEVELOPMENT Report by the Mexican Commission on Macroeconomics and health 3 The …
WHO GOOD PRACTICES FOR PHARMACEUTICAL …
www.who.intworking document qas/09.297/rev.2 page 2 schedule for the proposed adoption process of document qas/09.297/rev.2: who good practices for pharmaceutical microbiology laboratories
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Annex 3 WHO good manufacturing practices for ...
www.who.int96 Introduction The fi rst WHO draft text on good manufacturing practices (GMP) was prepared in 1967 by a group of consultants at the request of the Twentieth
Annex 5 WHO good distribution practices for …
www.who.int236 1. Introduction Distribution is an important activity in the integrated supply-chain management of pharmaceutical products. Various people and entities are
Annex 2 WHO good practices for pharmaceutical …
www.who.int71 Introduction and scope of document Pharmaceutical microbiology laboratories may be involved in: — sterility testing; — detection, isolation, enumeration and identifi cation of microorganisms
LABORATORY BIOSAFETY MANUAL - WHO
www.who.intinterim guidelines WHO/CDS/CSR/LYO/2003.4 LABORATORY BIOSAFETY MANUAL SECOND EDITION (REVISED) WORLD HEALTH ORGANIZATION Geneva 2003
Mycobacteriology Laboratory Manual - WHO
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Laboratory Guidelines for enumerating CD4 T …
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Guideline on similar biological medicinal products ...
www.ema.europa.euThe Guideline on similar biological medicinal products containing biotechnology -derived proteins as active substance: quality issues lays down the quality requirements for a biological medicinal product claiming to be similar to another one already marketed.
Guideline on similar biological medicinal products ...
www.ema.europa.euGuideline on similar biological medicinal products containing biotechnology -derived proteins as active substance: non-clinical and clinical issues (EMEA/CHMP/BMWP/42832/05 Rev.1) lays down the non-clinical and clinical requirements for a …
Isosteresin Medicinal Chemistry Group Meeting Christos ...
www.scripps.edubiological activity. Thornber(1979): Groups or molecules which have chemical and physical similarities producing broadly similar biological effects. Parameters affected with bioisostericreplacements Size, conformation, inductive and mesomericeffects, polarizability, H-bond formation capacity, pK a, solubility, hydrophobicity, reactivity, stability.
ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS
ec.europa.euThis medicinal product is subject to additional monitoring. This will allow quick identification of ... In order to improve the traceability of biological medicinal products, the name and the batch number . ... baseline, was similar to that seen in the general population. Reporting of suspected adverse reactions .
PRINCIPLES OF MEDICINAL CHEMISTRY
www.ysmubooks.ambetween chemical structure and biological activity, theories of drug action, and mechanism of ... Definition Medicinal chemistry, also called therapeutic chemistry, pharmaceutical chemistry, pharmacochemistry, and chemical pharmacy is that field of pharmaceutical sciences which applies the ... more active, and c) with similar or different ...
Transport route profiling qualification
www.who.intoverall size and weight should be similar to the container(s) used for the product(s) which are being monitored – this will ensure that the same handling practices are used. Warm life (test): The empty passive container is stabilized at +18.0°C and loaded with warm water-packs, which have been stabilized at the same temperature for a minimum of
Implementation Working Group ICH Q11 Guideline ...
database.ich.orgmeaning that the proposed starting material should be structurally similar to the drug substance. However, as stated in ICH Q11, this general principle is intended to help distinguish starting materials from reagents, catalysts, solvents, or other raw materials.