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						 FOLLOW UP ON GM FOODS
 During the last instalment, the conclusion was reached that GM foods should be
 Attached to a stringent code of labelling, to allow the customer to make an 
							informed decision.
 Each individual new product should undergo strict and long term studies for 
							after effects and possible harmful consequences.
 
 The following could be taken as a statement of intent.
 
 Objectives of GM foods
 Protection of crops against insects and viruses
 Increased herbicide tolerance
 If possible, to achieve these objectives together with a substantial cost 
							saving.
 
 GM crops have successfully increased yields, lowered costs of labour and 
							production and reduced the use of chemicals. Genetic engineering allows for 
							enhancement of food security and improves the nutritional quality which is not 
							possible with current technology. All this is due to the fact that the seed 
							contains already all these mentioned benefits.
 
 Some of these concerns have now been addressed and in the CIMMYT Newsletter of
 October 01, 2004 it has been established, that most objections on the risks of 
							GM foods are not backed by evidence current studies by national and 
							international organizations have shown no demonstrable harmful nutritional 
							effects on foods The effects on consumers are still outstanding
 or under study..
 
 The WHO (World Health Organization) has answered 20 most 
							commonly asked questions of WHO member State Governments
 1) A DEFINITION OF GM ORGANIZMS AND FOODS
 Organisms in which the DNA has been artificially (not in a natural way) altered 
							by transferring genes from one organism to another ( even between non- related 
							species).
 2) THE OBJECTIVES OF GM FOODS
 -A LOWER PRICE
 -BETTER DURABILITY, GREATER YIELDS AND / OR NUTRITIONAL VALUE, OR BOTH
 3) GM FOODS ARE ASSESED DIFFERENTLY THAN TRADITIONAL FOODS
 They are assessed on their effects / risks to human health and the 
							environment.
 This takes place prior to marketing.
 4) THE POTENTIAL RISKS TO HUMAN HEALTH ARE DETERMINED BY
 - Investigating toxicity
 No toxic affects of existing GM foods have been documented so far.
 - Allergenicity
 No allergenic effects of GM foods currently on the market have been found..
 - Gene transfer
 No genes to be transferred trough the digestive process from food to the 
							public.
 This could for instance include antibiotic resistance which is created in some 
							GM foods.
 ! There is a low probability of transfer. For this reason, the use of 
							antibiotic resistance genes has been discouraged by a WHO expert panel
 - Outcrossing ( the possible contamination of conventional crops in the wild by 
							means of cross pollination by insects and wind action)
 There is a real risk! This risk is being lowered by creating clear field 
							separation and
 Discussions on monitoring GM food products are underway at presen!
 5) RISK ASSESMENT FOR THE ENVIRONMENT
 Cover the GMO and the receiving environment, also including unintentional 
							effects.
 
 6+ 7) WHAT ISSUES CONCERN THE ENVIRONMENT?- Possible escape of genes into the wild population
 - Persistence of the gene after harvesting
 - Effects on non- target organisms ( insects , plants and humans)
 - Gene stability
 - Loss of bio diversity
 - Increased use of chemicals
 Currently under investigation are:
 -detrimental effects on beneficial insects, induction of resistant insects, 
							generation of new plant pathogens ( sicknesses),-detrimental consequences to 
							plant bio diversity and wildlife populations,- decreased use of current 
							principle of crop rotation ,the movement of herbicide resistant genes to other 
							plants.
 8) SAFETY OF GM FOODS
 -gm foods currently available have passed risk assessments. No adverse 
							effects on human
 health have shown. BUT
 CONTINUOUS RISK ASSESSMENT AND POST MARKET MONITORING ON ALL gm FOOD (EXISTING 
							AND NEW) IS IMPERATIVE!.
 
 9) CONTIUOUS TESTING AND LABELING REGIMES LEGISLATION IS CONTINUING TO 
								EVOLVE GM FOOD TO BE LABELLED IN SA.
 Labelling will be compulsory if there are significant differences of 
							composition and nutritional content against conventional foods. Storage and 
							preparation differences must also be noted on the label. Genes from animals or 
							humans must be declared on the label. Food improvements
 ( no allergens, more vitamins, less natural toxins ) must be proven and 
							certified.
 GM foods may be more expensive due to these testing procedures.
 Allergen containing foods including (crustaceans, eggs, fish, ground nuts, 
							milk, molluscs, Soya, tree nuts and wheat[gluten] must be labelled
 
 To preserve bio diversity, a system of Identity preservation ((IPS) for non- GM 
							foods is being developed by the SABS, the government and other stakeholders, to 
							allow consumers to choose between GM and non-GM products.
 NB
 Since 16 Jannuary 2006, all new applications for genetically modified organisms 
							are put on hold until the GMO amendment bill is revised (Public input on this 
							bill will be expected!
 
 10) GM FOOD ON THE NATIONAL MARKET
 MAIZE INSECT RESISTANT
 SOY BEAN HERBICIDE TOLERANT
 11) INTERNATIONAL TRADE OF gm FOODS, HOW IS IT GOVERNED?
 The CODEX ALIMENTARIUS (INTERNATIONAL FOOD CODE)
 DICTATES APRE MARKET ASESSMENT, CASE BY CASE, WHICH INCLUDES DIRECT AND 
							INDIRECT EFFECTS
 THE CARTAGENA PROTOCOL ON BIO SAFETY (CPB) is a LEGALLY BINDING TREATY
 Wwhich regulates the movement of living, modified organisms (LMO’s) which are 
							capable of transferring or replicating genetic material. CONSENT FROM IMPORTERS 
							IS needed before the first shipment.
 12) HAVE GM PRODUCTS CURRENTLY ON THE INTERNATIONAL MARKET PASSED A RISK 
								ASSESSMENT?
 YES. NO RISKS WERE FOUND.
 
 13) WHY HAS THERE BEEN CONCERN ABOUT FOOD SAFETY?
 Due to a number of food scares not necessarily related to GM foods
 14) THE EFFECT ON MARKETING GM FOODS IN THE EU
 A moratorium was placed on GM foods and they are subject to extensive 
							legislation.
 Mandatory monitoring of long term effects was introduced. \ Also mandatory 
							labelling. A minimum threshold of 1% DNA or protein resulting from gene 
							modification was introduced. No need for labelling below 1%! This was to avoid 
							accidental contamination of conventional food by GM material.
 15) THE STATE OF PUBLIC DEBATE
 The outcome differs from country to country. There is NO CONSENSUS BUT 
							SIGNIFICANT PROGRESS ON HARMONIZATION OF VIEWS FOR RISK ASSESMENT
 
 16) PEOPLES REACTIONS RELATED TO DIFFERENT ATTITUDES TO FOOD
 GENETIC Modification of foods can evoke a negative response, 
							depending on effective communication of risk assessment and cost benefits 
							evaluations.
 17) Implications to farmers rights to their own crops
 Yes , Intellectual property rights issues ( patent rights) have created 
							MONOPOLIZATION FEARS
 18) WHAT ABOUT THE GROWING INFLUENCE OF CHEMICAL INDUSTRIES ON
 AGRICULTURE?
 There is an undesirable level of control on seed markets. This may 
							lead to a reduction of available seeds to GM products only. With a 
							non-committant impact on the food basket of any society and on crop protection, 
							leading to farmer dependence.
 THIS CONTROVERY IS ONGOING!
 19) FURTHER DEVELOPMENTS IN THE gm FIELD
 -Crops with improved draught and disease resistance
 -Increased nutrient levels
 -Enhanced growth of fish- and plant species
 -Increased animal production of proteins used for vaccines
 20) WHAT IS THE WHO DOING TO IMPROVE EVALUATION OF GM FOODS?
 Develop a broader view. Not only considering food safety, but also 
							food security, social and ethical aspects, access and capacity building. 
							Striving to achieve international agreement on all GM food evaluations and 
							t4sting.
 CONCLUSION
 1) Development of GM foods is still taking place and will do so in the future.
 2) Controversy about the effects on peoples health are still ongoing (report by 
							BBC on 18/04/06 , 5a.m. news. The “Friends of the Earth” organisation in USA 
							has complained about the health effects, concentrating on allergenic products) 
							Safety reports have been rejected by them, as the safety testing was done 
							largely “ in House”. It seems, that only the manufacturers are geared to test 
							for this and no outside agencies have the materiel or machinery or the know how 
							to do this)
 3) Many countries do not have a labelling policy
 4) The controversy is ongoing watch this space!
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