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European Pharmaceutical Contractor

Editors' Letter

Back in 1996, when the original publisher of EPC invited me to become the Editor of the new magazine, I hardly anticipated the impact that the magazine would have. From a rather specialist publication it has developed into a broad ranging publication with editorial covering the whole waterfront of pharmaceutical development and beyond. In the 25 issues since, we have covered issues ranging from facts and figures about the CRO scene (perhaps my specialty), novel methods of drug discovery, electronic data capture, cutting-edge analytical techniques and literally hundreds more. Although the 'E' stands for European we have had special foci on Japan and other countries, including an article from Nelson Mandela, many articles from and about the US, as well as many looking at the developing industry in Eastern Europe and Scandinavia.

We have not neglected the vital areas of regulatory affairs or intellectual property, while we usually find room for an article on the commercial aspects of the pharmaceutical industry. It has sometimes been difficult to decide if an article is more suited to one of EPC's sister publications EBR or PMPS - but in the final analysis it has mattered little to our wide readership.

The publisher's staff have done much to make my job a pleasure, and much credit must go to the contributors themselves for keeping up such a high and lively standard. Nor must I forget the advertisers without whom EPC would not exist.


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By Dr Graham Hughes, Julia Lloyd-Parks
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Dr Graham Hughes
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Julia Lloyd-Parks
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Industry Events

6th European Forum for Qualified Person for Pharmacovigilance (QPPV)

24-26 April 2012, London, UK

This event is for European qualified persons for pharmacovigilance; deputy qualified persons; senior pharmacovigilance regulators and inspectors; CROs and consultants providing QPPV services; and national responsible persons for pharmacovigilance.
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