UK Parliament / Open data

Dietary Supplements: EU Law

Written question asked by David Tredinnick (Conservative) on Thursday, 25 October 2007, in the House of Commons. It was due for an answer on Friday, 19 October 2007. It was answered by Baroness Primarolo (Labour) on Thursday, 25 October 2007 on behalf of the Department of Health.

Question

(2) if he will make a statement on his planned future actions in relation to the setting of maximum permitted levels for vitamins and minerals in food supplements;

Answer

The Food Standards Agency (FSA) is responsible for food supplements issues and for negotiations relating to the European Commission (EC) Food Supplements Directive. No recent meetings have been held between Health Ministers and the European Commissioner concerning setting maximum permitted levels of vitamins and minerals in food supplements under this directive. Meetings will be held with stakeholders in early 2008 to discuss this issue.The bilateral meeting between the FSA and the EC on 12 September was held principally to gain insight into the Commission's intentions as regards the process by which maximum and minimum levels of vitamins and minerals in food supplements would be set. The Commission indicated that an orientation paper on setting maximum and minimum levels which it had issued in late July would be the starting point for discussions at working group level, which began on 24 September.The aim of the first working group meeting of 24 September was for the Commission to obtain member states' initial views on the orientation paper. We have been advised by the FSA that general discussions on the orientation paper in the working group revealed that many member states are yet to establish views on many issues. The Commission has asked member states to consider some of the issues presented in the orientation paper in preparation for more detailed discussions at the next working group meeting which has provisionally been scheduled for November and will be attended by FSA officials. We have been informed by the FSA that the Commission intends to produce draft amending legislation with respect to permitted levels of vitamins and minerals in food supplements by January 2009.We have been advised by the FSA that their officials met with their counterparts from the Republic of Ireland and other member states during, and in the margins of, the working group meeting on 24 September. The next working group meeting will provide further opportunity for bilateral discussions. The FSA currently has no additional meetings arranged to meet their counterparts in other member states outside working group meetings.The Government consider that the approach to regulation of food supplements should be safety-based and that consumers should have the right to make an informed choice unless their safety is compromised. Good progress has been made in promoting work carried out in the United Kingdom in establishing upper levels for vitamins and minerals and reference has been made to this in the Commission's orientation paper.We have been advised that the FSA is continuing its work on determining the potential economic impact of setting maximum levels to support future negotiations. In the absence of proposals from the Commission, a range of possible options is being considered. Until proposals are received and this work completed, the impact on small and medium sized enterprises of setting levels is unknown. We cannot, therefore, comment on the matter of compensation.There are no plans for Health Ministers to visit a specialist health food retailer to discuss the possible impact of setting of maximum levels of vitamins and minerals in food supplements.The FSA wrote to the governments of Jersey and Guernsey on 10 September concerning the trade in food supplements between these respective Crown Dependencies and the UK and suggesting a collective meeting with representatives of these governments. Copies of the letter sent by the FSA to the Bailiwick of Jersey have been placed in the Library. The release of the letter sent by the FSA to the Bailiwick of Guernsey is currently under consideration by the FSA under Section 36 of the Freedom of Information Act 2000 which precludes copies being placed in the Library at this time.The Medicines and Healthcare products Regulatory Agency (MHRA) believes that herbal remedies from the Channel Islands are subject to the Traditional Herbal Medicines Directive 2004/24/EC. The MHRA has already begun discussions about this with the Government of Guernsey and wrote to the Government of Jersey to open discussions on 28 June 2007. Copies of the MHRA's recent letters to the Bailiwick of Guernsey and letter to the Bailiwick of Jersey have been placed in the Library.

Type
Written question
Reference
159993; 465 c551-3W
Session
2006-07
Deposited Paper DEP2007-0037
Thursday, 25 October 2007
Deposited papers
House of Commons
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