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European Journal of Clinical Pharmacology

Volumn 67, Issue 11, 2011, Pages 1199-1200

Anything new in EU pharmacovigilance?

(2) Garattini, Silvio a Bertele', Vittorio a

a MARIO NEGRI INSTITUTE FOR PHARMACOLOGICAL RESEARCH (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

PLANT MEDICINAL PRODUCT;

CLINICAL EVALUATION; DRUG LEGISLATION; DRUG MARKETING; DRUG MISUSE; DRUG MONITORING; DRUG SAFETY; DRUG SURVEILLANCE PROGRAM; FUNDING; HEALTH CARE ACCESS; MEDICATION ERROR; NOTE; POSTMARKETING SURVEILLANCE; PRIORITY JOURNAL; PUBLIC HEALTH SERVICE; RISK ASSESSMENT; RISK BENEFIT ANALYSIS;

ADVERSE DRUG REACTION REPORTING SYSTEMS; DATABASES, FACTUAL; EUROPEAN UNION; GOVERNMENT REGULATION; INTERNATIONAL COOPERATION; LEGISLATION, DRUG; PHARMACOVIGILANCE; RISK ASSESSMENT;

EID: 80054738894 PISSN: 00316970 EISSN: 14321041 Source Type: Journal
DOI: 10.1007/s00228-011-1052-1 Document Type: Note

Times cited : (8)

References (4)

1
- 84857504689
- Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use
- Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products. Available at: http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2010:348:0001:0016: EN:PDF
- Regulation (EC) No 726/2004 Laying Down Community Procedures for the Authorisation and Supervision of Medicinal Products for Human and Veterinary Use and Establishing A European Medicines Agency, and Regulation (EC) No 1394/2007 on Advanced Therapy Medicinal Products

2
- 80051527933
- Directive 2010/84/EU of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance
- Directive 2010/84/EU of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use. Available at: http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2010:348:0074:0099: EN:PDF
- Directive 2001/83/EC on the Community Code Relating to Medicinal Products for Human Use

3
- 77955551374
- Risk management plans: Are they a tool for improving drug safety?
- 10.1007/s00228-010-0848-8 20577875 10.1007/s00228-010-0848-8 1:CAS:528:DC%2BC3cXptVaiurc%3D
- S Frau M Font Pous MR Luppino A Conforti 2010 Risk management plans: are they a tool for improving drug safety? Eur J Clin Pharmacol 66 785 790 10.1007/s00228-010-0848-8 20577875 10.1007/s00228-010-0848-8 1:CAS:528:DC%2BC3cXptVaiurc%3D
- (2010) Eur J Clin Pharmacol , vol.66 , pp. 785-790
- Frau, S.¹ Font Pous, M.² Luppino, M.R.³ Conforti, A.⁴

4
- 77957889740
- Rosiglitazone and the need for a new drug safety agency
- 10.1136/bmj.c5506 10.1136/bmj.c5506
- S Garattini V Bertele' 2010 Rosiglitazone and the need for a new drug safety agency Br Med J 341 c5506 10.1136/bmj.c5506 10.1136/bmj.c5506
- (2010) Br Med J , vol.341 , pp. 5506
- Garattini, S.¹ Bertele, V.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.