메뉴 건너뛰기




Volumn 131, Issue 1-2, 2002, Pages 137-143

Environmental risk assessment for new human pharmaceuticals in the European Union according to the draft guideline/discussion paper of January 2001

Author keywords

Draft Guideline 2001; Environmental risk assessment; European Union; Pharmaceuticals; Tiered assessment

Indexed keywords

DRUG; DRUG METABOLITE;

EID: 0037052862     PISSN: 03784274     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-4274(02)00049-8     Document Type: Article
Times cited : (39)

References (15)
  • 2
    • 0009037799 scopus 로고    scopus 로고
    • CEC. 1998b. Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market. Off. J. L123 (24/04/1998), 1-63
  • 4
    • 0008998062 scopus 로고    scopus 로고
    • CEEC, 1965. Council Directive 65/65/EEC of 26 January 1965 on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products. Off. J. 22 (09/02/1965), 369-373
  • 5
    • 0009052255 scopus 로고    scopus 로고
    • CEEC, 1991. Council Directive 91/414/EEC of 15 July 1991 concerning the placing of plant protection products on the market. Off. J. L230 (19/08/1991), 1-32
  • 6
    • 0009008598 scopus 로고    scopus 로고
    • CEEC, 1992. Council Directive 92/32/EEC of 30 April 1992 amending for the seventh time Directive 67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances. Off. J. L154 (05/06/1992), 1-29
  • 7
    • 0009008599 scopus 로고    scopus 로고
    • CEEC, 1993a. Council Directive 93/39/EEC of 14 June 1993 amending Directives 65/65/EEC, 75/318/EEC and 75/319/EEC in respect of medicinal products. Off. J. L214 (24/08/1993), 22-30
  • 8
    • 0009052256 scopus 로고    scopus 로고
    • CEEC, 1993b. Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products. Off. J. L214 (24/08/1993), 1-21
  • 10
    • 0009050341 scopus 로고    scopus 로고
    • Opinion on: Draft CPMP discussion paper on environmental risk assessment of medicinal products for human use [non-GMO containing]
    • C2/JCD/csteeop/CPMPpaperRAssessHumPharm12062001/D(01), Brussels, 12 June 2001
    • (2001) 24th CSTEE Pleanry Meeting
  • 11
    • 0008963217 scopus 로고    scopus 로고
    • ECB, 1999. Technical Guidance Document in Support of Commission Directive 93/67/EEC on Risk Assessment for New Notified Substances and Commission Regulation (EC) No. 1488/94 on Risk Assessment for Existing Substances. Office for Official Publications of the European Communities, Luxemburg


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.