Sentence examples similar to agency of evaluation from inspiring English sources

The European Agency for Evaluation of Medicinal Products criterion of serologic response to influenza vaccines, a SRH value of >25 mm2, was used as a cut-off for serologic protection [26].

Notably, one proteasome inhibitor (bortezomib) has been recently approved by both the Food and Drug Administration (USA) and the European Agency for Evaluation of Medicinal products for the treatment of recurrent multiple myeloma and is currently undergoing clinical trials for AIPCa (Papandreou and Logothetis, 2004; Papandreou et al, 2004; Price and Dreicer, 2004; Zavrski et al, 2007).

www.emea.europa.eu/ The European Medicines Agency EMEAA) is a European Agency for evaluation of medicinal products.

Forty-four of these documents were published by the Swedish Medical Products Agency [ 16], 13 by the Swedish Agency for Evaluation of Medical Technologies [ 17] and 53 (in three booklets) by the Swedish Strategic Programme for The Rational Use of Antimicrobial Agents and Surveillance of Resistance (STRAMA) [ 18], established in order to prevent bacterial resistance to common antibiotics.

The agency's evaluation of the significance of government hiring--which has been sizable this year--is also seen as a distortion of the jobs numbers even though government jobs represent just 17% of total employment.

The agency's evaluation of glyphosate saw "limited evidence" of a type of cancer called non-Hodgkin lymphoma, as seen in studies in the United States, Sweden and Canada conducted among farm workers since 2001.

He saw it growing up with Roosevelt's New Deal and then again as a member of Sargent Shriver's Peace Corps, where he served as the agency's first director of evaluation.

Qualitative results suggested that aspects of communication (awareness and positive attitudes) and agency directors' evaluation of resources, balanced against intervention complexity and flexibility, competing priorities, and mandates, influenced adoption.

In 1998, the genetically engineered humanized monoclonal antibody (palivizumab) was granted FDA Food and Drug Administrationn) approval for prophylaxis of high-risk children in the United States; EMEA (European Agency for the Evaluation of Medicinal Products) approval followed in 1999 for Europe.

The Food and Drug Administration FDAandand the European agency for the evaluation of medical products have approved the use of BMP-2 as bone graft substitute in adults with open tibial fractures and those undergoing anterior lumbar inter-body spinal fusion as an adjunct to standard care by internal fixation [6, 7, 8, 9, 10].

At the European Union level, The European Agency for the Evaluation of Medicinal Products EMEAA) is responsible for the implementation of the European Risk Management Strategy (ERMS) [ 51].