Guidance on methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non-allowed pharmacologically active substances present in food of animal origin

EFSA Journal

Volumn 11, Issue 4, 2013, Pages

[No Author Info available]

Author keywords

non allowed pharmacologically active substances; RALLOQ; RPA; TBLOQ; TSV

Indexed keywords

EID: 85032154937     PISSN: None     EISSN: 18314732     Source Type: Journal    
DOI: 10.2903/j.efsa.2013.3195     Document Type: Article

References (4)

1. CRL Guidance Paper, 2007. CRL Guidance paper (7 December 2007). CRLs view on state of the art analytical methods for national residue control plans. 8 pp. Available online: www.bvl.bund.de/SharedDocs/Downloads/09_Untersuchungen/EURL_Empfehlungen_Konzentrationsauswahl_Methodenvalierungen.pdf?__blob=bublicationFile.
2. EFSA Scientific Committee, 2012a. Scientific Opinion on Exploring options for providing advice about possible human health risks based on the concept of Threshold of Toxicological Concern (TTC). EFSA Journal 2012;10(7):2750, 103 pp.
3. EFSA Scientific Committee, 2012b. Guidance on selected default values to be used by the EFSA Scientific Committee, Scientific Panels and Units in the absence of actual measured data. EFSA Journal 2012;10(3):2579, 32 pp.
4. EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP), 2012c. Guidance for establishing the safety of additives for the consumer. EFSA Journal 2012; 10(1): 2537, 12 pp.