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The Pharmaceutical Journal Vol 265 No 7108 p185
August 5, 2000 News

NPA board

Welcome for EC's proposed food supplement safety measures

The National Pharmaceutical Association's board of management has welcomed the European Commission's intention that a proposed directive on food supplements should set maximum safe levels.
Noting that the proposed directive was designed to ensure both safety and free trade within the European Community, the board was, however, concerned to clarify the status of nutrients that were not covered in a new "positive" list of vitamins and minerals issued by the commission. The board approved an NPA response to the proposal pointing out that many existing products on the United Kingdom market contained ingredients such as fish oils and evening primrose oils that were not on the positive list.
The NPA response also strongly disagreed with the proposal that member states could opt out of imposing a procedure of notification of the marketing of a food supplement to competent authorities if they felt it to be "too burdensome".
The board welcomed proposals to label vitamin and mineral supplements with information about their use, and to introduce compulsory nutrition labelling.
The following are among other matters considered by the board at its July meeting.

Vitamins
Vitamin supplements: the NPA board welcomes proposals for compulsory nutrition labelling

NPAnet The board was advised that the second phase of NPAnet would be launched in late summer. Subscribers would be able to download standard forms to adapt for their own use, access information leaflets online, and order business-to-business products and services. Business intelligence would be available from the Intrapharm network and a daily news service would be offered.

E-pharmacy code of conduct The board learnt that the Pharmaceutical Group of the European Union (PGEU) was to establish a European code of conduct for electronic pharmacy services. Because pharmacy regulations varied between countries, it would be a broad framework to which member states could add details of practice standards and guidelines. The UK would be represented on the working group that will be formulating the guidelines.