| Document Date: 2013-07-21 04:57:35
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City London / / Company IgG / NEC / Ad Hoc Group / / / Event Product Issues / / Facility Canary Wharf / / / IndustryTerm authorised medicinal products / patient / magnetic resonance imaging / assisted reproductive technology / trial protocol / antibiotic medicinal products / enzymatic microsomal systems / clinical trial protocols / multiparameter cytofluorimetric technology / medicinal products / energy / given medicinal product / organ systems / medicinal product / protein carrier systems / expected medicinal product / orphan medicinal products / / MedicalCondition immediate immune deficiency / hydrocephalus / seizures / respiratory distress syndrome / low blood pressure / injury / concomitant diseases / perinatal brain injury / severe disease / Hypoglycemia / infections / bilirubin encephalopathy / premature birth / paralysis / intrauterine growth retardation / disease / example intrauterine growth retardation / patent ductus arteriosus / pulmonary function / cardiopulmonary dysfunction / e.g. nephrocalcinosis / enterocolitis / diseases / infection / kernicterus / / MedicalTreatment enteral feeding / assisted reproductive technology / parenteral nutrition / immunosuppression / catheter / / Organization FORMULATIONS AND ROUTE OF ADMINISTRATION / COMMITTEE FOR MEDICINAL PRODUCS FOR HUMAN USE / Paediatric Working Party / AND PAEDIATRIC COMMITTEE / / / Position EXECUTIVE / / Product interaction / / ProgrammingLanguage EC / / Technology genomics / drug metabolism / X-ray / tomography / antibodies / ultrasound / stem cells / trial protocol / MRI / multiparameter cytofluorimetric technology / clinical trial protocols / assisted reproductive technology / Pharmacokinetics / Pharmacogenetics / magnetic resonance imaging / spectroscopy / pharmacodynamics / / URL http /
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European Medicines Agency Evaluation of Medicines for Human Use London, 25 June 2009 Doc. Ref. EMEACOMMITTEE FOR MEDICINAL PRODUCS FOR HUMAN USE (CHMP)