Select Committee on Agriculture Appendices to the Minutes of Evidence


APPENDICES TO THE MINUTES OF EVIDENCE


APPENDIX 1

Memorandum submitted by the Secretary General, Animal Health Distributors Association (UK) Ltd (B 1)

  Thank you for your letter of 3 March. I am pleased that the committee is going to look into the issue, however, in my view, this should be on a constructive basis, ie where do we go from here, and how do we get there. I would be totally opposed to a witch hunt in respect of the decision of 20 December and what went before, despite my belief that it could have been handled much more satisfactorily from all sides. However, it may be helpful if the Committee were to recommend that if a similar situation were to arise in future government should bring together manufacturers, distributors and users immediately before the announcement is made, to work out the least damaging and most effective means of recall and an appropriate and practical timetable.

  Turning to the future, I can do no better than repeat extracts from my letter to the Minister, of 11 February, of which you have a copy—indeed whether because of the letter, or coincidentally with it, most of the suggestions contained in it seem to be happening—last week, this week and next week. Thus I hope this constructive phase is permanent.

  As I said to the Minister on 11 February:

    "The first problem is that without OP dips the sheep industry faces an increasingly serious disease and animal welfare problem—alternative dips will be overused and as was said by their own manufacturer yesterday, may become ineffective in large parts of the UK by the end of this year. Injections of endecticide will not and cannot solve the problem on a nationwide basis. The second problem is that it is politically impossible, I fully recognise this, for you to reject advice received from a regulatory committee such as the VPC, or to have second thoughts after lobbying from industry and tell them to change their advice to you!"

  I went on to emphasise the vital aspects of the VPC's advice on which the 20 December announcement was based:

    "Point 8.3.2.I is the key. VPC remind you that they requested urgent design changes in July 1999. They then go on to say that they have seen plans from manufacturers for changes, but that they `advise that remaining marketing authorisations should be suspended until the design of containers is improved to minimise the risk of exposure to OP concentrate and/or clear plans are in place to effect the necessary improvements'. By using the `and/or' this advice leaves it to you to decide whether to wait until changes are in place, or to end the suspension when the plans alone are in place—ie the suspensions could be ended from a specific future date on the basis that product is marketed in accordance with the plans submitted and agreed."

  I went on to conclude:

    "Therefore the issue is for the VPC to be satisfied that the `necessary improvements' have been `effected'. Would it not be possible following yesterday's meeting, for you to write to the VPC, informing them of the extreme risk of an animal welfare crisis of which you have been advised, following your adoption of their advice on OPs, and asking them for a further report, by 31 March 2000, on the progress that is being made by marketing authorisation holders in developing plans, acceptable to them, the VPC, that would `effect the necessary improvements', so that the suspension of market authorisations could be lifted on or before 31 May 2000. Such a request of VPC could encourage them to cut through some of the unnecessary traditional bureaucracy and formal appeal procedures associated with market authorisations, which would in this case waste time we do not have. It would persuade them to actually discuss with market authorisation holders what is possible in order to meet their requirements—which are, we must remember, to `minimise' and not, however desirable to HSE, to `eliminate' the risk, which is impossible."

    "I also suggest that as part of the package for ending the suspension of market authorisations, the idea which was put over at the meeting, that it be made a specific legal requirement that only the Certificate of Competence holder is allowed to handle concentrated OP dip—something that AHDA pressed for when the C of C was first introduced."

  Finally, I mention to you the final point of my letter to the Minister—point 8.3.3.1 of the VPC's regulatory advice. This stated that "Ministers should re-emphasise to merchants the importance of ensuring that purchasers of sheep dips are fully aware of the potential hazard of exposure to sheep dip". It was not made clear earlier in the VPC advice (point 6.9) that it was AHDA, representing most of those supplying dips to farmers, who first proposed that this laminated A4 sheet should be produced and distributed. Indeed, the original AHDA proposal was that this A4 laminated sheet should be made legally part of the required labelling of each dip container, so that it was a legal requirement that one was handed over with every container of dip purchased. We proposed this so that it was not necessary for a farmer to lift a container of dip (possibly open) to head height in order to be able to read the safety advice. Unfortunately this proposal, which would have been far more effective than that which was eventually adopted, was watered down as being impractical by others prior to the distribution route by AMTRA and NPTC being agreed. I return to this idea and suggest that when the suspensions are lifted, these A4 sheets are made a legal part of the labelling requirements to be handed over with each sale of dip.

6 March 2000


 
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