As 1992 looms on the horizon and preparation is made for the
completion of the internal market in Europe, the CMR realised the
value of addressing some of the issues involved and defining the
objectives and achievements of medicines regulations in a number of
EEC countries in comparison with Japan and the USA. The overall aim
was to use the lessons of past experience to determine the most
appropriate way forward. The final debate focused on two
possibilities for assessing and granting marketing authorisations
for Europe, namely mutual recognition or a centrally organised
European Med icines Office. These two views were discussed in
detail at both the workshop at the Ciba Foundation and the
international symposium at the Royal College of Physicians. It is
hoped that this sharing of ideas and the publication of the
proceedings of this fifth CMR Workshop will have encouraged all
concerned to continue the debate so that the final outcome will be
the establishment of an efficient system in the community for the
benefit of patients, the practising physician and the
pharmaceutical industry. We would like to take this opportunity of
thanking Brenda Mullinger for the considerable amount of scientific
and editorial work that she carried out on the manuscripts, Sheila
Wright for providing the secretarial support which allowed the
proceedings to be submitted to Kluwer Academic Publishers on disk
and Sandra Cox who organised the administrative aspects so vital to
the successful running of a Workshop and major international
symposium. S. R."
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