Oral medicine acceptance in infants and toddlers: measurement properties of the caregiver-administered Children’s acceptance tool (CareCAT)
Author:
Funder
Universitetet i Bergen
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1186/s12887-018-1080-4.pdf
Reference37 articles.
1. EMA. Guideline on pharmaceutical development of medicines for paediatric use. 2013. http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2013/07/WC500147002.pdf Accessed 21 Apr 2017.
2. FDA. Pediatric Study Plans: Content of and process for submitting initial pediatric study plans and amended initial pediatric study plans. Guidance for industry. 2013. https://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm360507.pdf . Accessed 25 Apr 2017.
3. Ranmal S, Tuleu C. Demonstrating evidence of acceptability: the “Catch-22” of pediatric formulation development. Clinical Pharmacology & Therapeutics. 2013;94:582–4.
4. Kozarewicz P. Regulatory perspectives on acceptability testing of dosage forms in children. Int J Pharm. 2014;469:245–8.
5. Sjovall J, Fogh A, Huitfeldt B, Karlsson G, Nylen O. Methods for evaluating the taste of paediatric formulations in children: a comparison between the facial hedonic method and the patients' own spontaneous verbal judgement. Eur J Pediatr. 1984;141:243–7.
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