Year of publication
Type of media
Subject
Type of material
Licence
Language
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International harmonisation – the need for transparency
IOS Press | 1996International harmonisation of drug regulatory procedures could contribute both to efficiency and to drug safety. The International
... -
Food and Drug Administration Pesticide Program Residue Monitoring, 1997
NTIS | 1997This is the eleventh annual report summarizing the results of the Food and Drug Administrations (FDA) pesticide residue monitoring program ...Publisher: Food and Drug Administration, Washington, DC -
ISBC 2012 17th International Symposium on Bioluminescence and Chemiluminescence
Wiley | 2012pharmacometrics assay system of drug‐induced effect during embryogenesis, we established bioluminescent transgenic Drosophila of the armadillo and applied ... -
Efficacy and Cardiovascular Safety of SGLT2 Inhibitors
Bentham Science Publishers | 2021|). The latter has recently been recognised as a major cause of morbidity and mortality in patients with diabetes mellitus. There had been an ...Keywords: Clinical Trials & Regulatory Affairs, Drug Design and Discovery -
Hepatic Effects of Duloxetine-II: Spontaneous Reports and Epidemiology of Hepatic Events
Bentham Science Publishers | 2008|cumulative spontaneous reporting rate of all duloxetine hepatic-related events combined was 0.00799%, in the context of other drug-induced hepatic ...Keywords: Clinical Trials & Regulatory Affairs, Drug Design and Discovery -
Safety of Inhaled Fluticasone Propionate Therapy for Pediatric Asthma - A Systematic Review
Bentham Science Publishers | 2013|Context and Aim: Asthma is a common problem in paediatric population. International treatment guidelines recognize the role of inhaled ...Keywords: Clinical Trials & Regulatory Affairs, Drug Design and Discovery -
Regulations of Cosmetics Across the Globe
Bentham Science Publishers | 2015|of regulatory information for Canada, United States, European Union and India were available at website maintained by their respective ...Keywords: Code of federal regulations, international nomenclature for cosmetic ingredients, Clinical Trials & Regulatory Affairs -
Single-Laboratory Validation of a Multitoxin Ultra-Performance LC-Hydrophilic Interaction LC-MS/MS Method for Quantitation of Paralytic Shellfish Toxins in Bivalve Shellfish
Online Contents | 2015|A single-laboratory validation study was conducted for the hydrophilic interaction-LC-MS/MS analysis of paralytic shellfish toxins (PSTs ...Keywords: Drug Residues - analysis -
Role of Different Peptides for Cancer Immunotherapy
Online Contents | 2021|based on peptides by imitating the biological functions of protein having extremely specialized immuno-regulatory roles has been the subject of ...Keywords: Drug delivery -
Structure-based investigation of pyruvate dehydrogenase kinase-3 inhibitory potential of thymoquinone, targeting lung cancer therapy
Elsevier | 2024|phosphorylation” (OXPHOS) in mitochondria. The pyruvate dehydrogenase kinases (PDKs) have many regulatory roles in energy generation balance by ...Keywords: Drug design and discovery
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