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Genetically Modified Crops (PE470)
Item 4 concerns petition PE470 on genetically modified crops. The petition was submitted on behalf of the Munlochy vigil to end the farm-scale trials of GM oil-seed rape, which is modified to resist herbicides. The Transport and the Environment Committee has forwarded the petition to us, having previously considered a similar petition from Friends of the Earth Scotland, which I think the Rural Affairs Committee also considered.
There is a job of work for us to do. The previous inquiries have concentrated largely, but not exclusively, on the environmental impact of GM crops. We need to consider more closely the alleged or potential public health implications.
I spoke to Charles Saunders from the BMA after he gave evidence this morning. He said that there are no data on the impact of GM crops on public health. In fact, at the end of the trials at Munlochy, we will know more about the effects of GM crops on moths, beetles and butterflies than on public health. He also said that the BMA wrote to the health department two months ago and has still not received a reply.
Let me establish what your suggestion is. We have to acknowledge that we are approaching the summer recess. There is a work load issue for when we come back, because we will have a contentious bill to consider, which will be time consuming. Nicola Sturgeon has put forward her suggestion; what do you propose we do at this stage, Mary?
I suggest that we take evidence from the Minister for Health and Community Care and representatives of the Scottish Executive health department. I would like to hear evidence from the BMA and from Professor Hooper of the University of Sunderland, who has done a considerable amount of research into the effect of GM crops on public health.
So you are suggesting a full inquiry. Bear in mind that, once we open that up, we have to hear from everybody, to be fair.
We have to hear from both sides, but we have to hear from the people whom I mentioned. Professor Hooper's comments make quite frightening reading. I know that time is not on our side, but we have to reassure people about public health. We cannot just leave it.
Could we hold a special meeting early in the recess to handle this? It is a serious issue. The problem is that the crops are flowering right now.
I would find that suggestion a bit difficult.
We have to keep in mind the fact that the Transport and the Environment Committee was sufficiently worried by the petition to recommend to the Minister for Environment and Rural Development that the field trial be ended and the crop ploughed into the ground. That committee took the issue very seriously. It did not feel qualified to comment on the field trials' health implications, but felt that those should be pursued. That is why the petition was referred to this committee. We cannot just ignore the matter; we have to do something about it. The question is; what do we do?
Let me pick up on the point that Nicola Sturgeon made about timing. If we knew that we were to hear from the minister next week, I do not feel that I have enough background information to do justice to that opportunity. I would be surprised if most other members did not feel the same. If we had a reporter working over the summer and then considered whether to take further evidence on that basis as soon as we return after the recess, that would probably be the best solution, given the time scale available.
I think that that is the way to go. I would be happy to do some work on the matter over the summer, contacting the relevant people so as to form a view on whether it would be desirable for us to inquire fully into the matter and, if so, on whom to invite to speak to us. If we let the matter lie over the summer, we would not be giving due consideration to the seriousness and urgency of the issue.
The chief medical officer for Scotland was at a meeting with the Medical Research Council that John McAllion and I attended. We all know that there is a lot of conflicting evidence. As a responsible committee, we want to make the best judgment that we can. Would it be possible for us to ask the CMO to ask someone on the Medical Research Council to review the evidence and give us a steer, rather than tying up a member of the committee?
I think that the only way to go forward is by accessing as many different points of view as possible. I have only one concern. I take on board the comments and the offer that Nicola Sturgeon has made and that is very good. However, we were in a comparable situation in relation to the measles, mumps and rubella vaccine report, for which we agreed to have one reporter, Mary Scanlon. On reflection, I think that we made a mistake because it was too much work for one person and it was very technical. We did not appreciate at the outset what a difficult task we had set. We might go down the reporter route, but I think that the situation is similar to that of the MMR report and that we might need a second reporter or perhaps require SPICe involvement at a much earlier stage. I put that suggestion into the melting pot. On reflection, I felt guilty that the Health and Community Care Committee had, because of the nature of the inquiry, put too much on the shoulders of one individual.
We are not necessarily looking for someone to go away and come back with definitive conclusions. We need someone to make preliminary inquiries and suggest a way forward for the committee. That way forward might be a full inquiry or involve taking evidence from a few people. We do not need someone to come back to us by the end of the summer and say that GM crops are safe or not. I would share your concerns if that were what was expected. My concern is that we make progress over the summer. If we do not, we will miss the opportunity to do anything on the subject.
Certain key people, such as the MRC, the BMA, the petitioners and local residents, have to be contacted over the summer or we will not make the best use of the time. I take on board that point.
Perhaps the committee could write to some of the people who might wish to make submissions in relation to health or tell us where we can find the health information. It should be easy to get a few names to give us a kick start. We all suspect that there is very little information in relation to human health.
If we decided to appoint a reporter, the committee would make such an inquiry. The information would be put on the website that the reporter, on behalf of the committee, was seeking information on the health aspects of GM. It would be up to the reporter to take forward all the work that they were able to over the recess. After the recess the committee as a whole could make a judgment about the next steps on the basis of that work.
In our advertising we need to be specific about the fact that the individual reporter would be acting as a sieve for the committee, finding out what evidence is available, what is relevant and what the committee could undertake. The reporter would look at all the material available and suggest the direction that the committee should take. We need to be specific about the remit of the reporter.
The problem is that there are no data on public health. That is what Charles Saunders was saying. Even if we recommend a study, there are no data, which is why the BMA, the MRC and the people in Munlochy are so concerned.
That is for the reporter to investigate and substantiate. For example, I understand that the schemes that are in place—obviously we are not at the forefront in this and other countries are much farther down the road—require to have on-going monitoring.
I thank Nicola Sturgeon for that.
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