Results 61 to 70 of about 2,350,416 (333)

Bioequivalence and Pharmacokinetics of Low-Dose Anagrelide 0.5 mg Capsules in Healthy Volunteers

open access: yesBiomedicines
Objectives: Anagrelide, an oral phosphodiesterase-3 inhibitor, is widely used to treat thrombocythemia. Evaluating the bioequivalence of low-dose formulations is essential to ensure consistent therapeutic outcomes while minimizing adverse effects ...
Ahmet Inal   +7 more
doaj   +1 more source

Good documentation practice in clinical research

open access: yesPerspectives in Clinical Research, 2011
One of the most common inspection findings in investigator site inspections is lack of reliable, accurate and adequate source documentation. This also happens to be the most common pitfall identified during sponsor audits.
Chitra Bargaje
doaj   +1 more source

Systematic review of new medics’ clinical task experience by country [PDF]

open access: yes, 2014
OBJECTIVES: There is a need for research which informs on the overall size and significance of clinical skills deficits among new medics, globally. There is also the need for a meta-review of the similarities and differences between countries in the ...
Dickson GD   +4 more
core   +1 more source

Changes in Body Composition in Children and Young People Undergoing Treatment for Acute Lymphoblastic Leukemia: A Systematic Review and Meta‐Analysis

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Ongoing evidence indicates increased risk of sarcopenic obesity among children and young people (CYP) with acute lymphoblastic leukemia (ALL), often beginning early in treatment, persisting into survivorship. This review evaluates current literature on body composition in CYP with ALL during and after treatment.
Lina A. Zahed   +5 more
wiley   +1 more source

Good clinical practice

open access: yesGinekologia polska, 1995
The term Good Clinical Practice (GCP) suggests that it relates to a standard of practical clinical medicine; it does not. It is a standard, or more precisely, a set of standards that have been developed for the conduct of clinical trials with investigative new drugs. These standards can actually be applied to any experimentation in humans.
Adam Cohen, John Posner
openaire   +3 more sources

New version of the Pediatric Evaluation of Disability Inventory (PEDI-CAT): translation, cultural adaptation to Brazil and analyses of psychometric properties [PDF]

open access: yes, 2016
BACKGROUND: The Pediatric Evaluation of Disability Inventory-Computer Adaptive Test (PEDI-CAT), developed with innovative measurement methodologies, evaluates functioning of children and youth, from 0 to 21 years, with different health conditions.
Amaral, Maíra F.   +5 more
core   +3 more sources

Parent‐to‐Child Information Disclosure in Pediatric Oncology

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Despite professional consensus regarding the importance of open communication with pediatric cancer patients about their disease, actual practice patterns of disclosure are understudied. Extant literature suggests a significant proportion of children are not told about their diagnosis/prognosis, which is purported to negatively ...
Rachel A. Kentor   +12 more
wiley   +1 more source

Enhancing Clinical Research Professionals’ Training and Qualifications (ECRPTQ): Recommendations for Good Clinical Practice (GCP) training for investigators and study coordinators

open access: yesJournal of Clinical and Translational Science, 2017
Introduction The translation of discoveries to drugs, devices, and behavioral interventions requires well-prepared study teams.
Thomas P. Shanley   +21 more
doaj   +1 more source

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