Medicine Information Network for Europe

Abstract

Rapid advances in Information Technology and the increasing use of the Internet introduce a completely new vehicle for the dissemination of information on medicinal products that is not limited to regulators or health practitioners, but accessible to everybody. This paper presents the Medicines Information Network for Europe (MINE) system, a network based application aimed at establishing a coherent, comprehensive European Data Centre for collecting and making available accurate and up-to-date official information about medicinal products authorised in the European Union.

Keywords

medicinal product database information dissemination network document management market authorisation

Get full access to this article

View all access options for this article.

References

CEN/TC 251, European Standardization of Health Informatics; http://www.centc251.org.

Directorate General for Research (2000) New Technologies for the Marketing and Sale of Medicines on the Internet and Television Networks. Brussels: European Parliament, Directorate General for Research.

Petersen

(2001) The inevitability of E-commerce [Online]. Posted on: http://www.managedcaremag.com/archives/9906/9906.ecomm.html.

Working Group on Pharmaceuticals and Public Health (2000) Pharmaceuticals and public health in the EU: proposals to the high level committee on health for policies and actions in the framework of the Treaty of Amsterdam. Brussels: EU Commission Working Group on Pharmaceuticals and Public Health.

Council of the EEC (1993) Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products. Brussels: Council of the EEC; Council Regulation (EEC) No 2309/93.

Council of the EEC (1965) Approximation of provisions laid down by law, regulation or administrative action relating to medicinal products. Brussels: Council of the EEC; Council Directive 65/65/EEC.

Council of the EEC (1975) Approximation of provisions laid down by law, regulation or administrative action relating to medicinal products. Brussels: Council of the EEC; Council Directive 75/319/EEC.

Council of the EEC (1992) Labelling of medicinal products for human use and on package leaflets. Brussels: Council of the EEC; Council Directive 92/27/EEC.

EU Commission (1995) Examination of variations to the terms of a marketing authorisation granted by a competent authority of a Member State. Brussels: EU Commission; Regulation no 541/95.

10.

EU Commission (1995) Examination of variations to the terms of a marketing authorisation falling within the scope of Council Regulation (EEC) No 2309/93. Brussels: EU Commission; Regulation (EC) No 542/95; http://www.ashursts.com/practice/it/report.htm.

11.

EU Commission (1996) Examination of an application for the transfer of a marketing authorisation for a medicinal product falling within the scope of Council Regulation (EEC) No 2309/93. Brussels: EU Commission; Regulation (EC) No 2141/96.

12.

EU Commission (1997) Medical informatics – medicinal product identification. Brussels: EU Commission; preENV CEN 12610.

13.

Pagliari

Rana

(2000) The Unified Tracking System (UTS) medicinal product data model. Ispra, Italy: European Commission Joint Research Centre; JRC Technical Note I.00.142.