{"product_id":"ags-international-technical-guidelines-pack-genetically-modified-foods-regulatio","title":"International Technical Guidelines Pack - Genetically Modified Foods Regulation","description":"\u003cp\u003e\u003cem\u003eA genetically modified consignment is judged by its destination, its threshold and its own dossier, and every limb of that test is documented here.\u003c\/em\u003e\u003c\/p\u003e\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eFew areas of food law turn on so small a number. The one per cent per-ingredient threshold, and the second limb attached to it, decide whether a product is labelled, admitted or refused, while the declared destination — food, feed or planting — decides which regime applies at all. This set covers that machinery in full, prepared as international editions of GSO 2141, GSO 2142 and GSO 2143 on the normative basis of the Cartagena Protocol on Biosafety and the Codex biotechnology texts.\u003c\/p\u003e\u003cp\u003eUnprocessed commodities are controlled at consignment level, through approvals, the consignment register, the certified document and strict separation of the food, feed and planting destinations. Processed products that contain, consist of or are produced from GMOs bring in conditions of market entry, nutritional equivalence and the identification of transferred allergens. Assessment completes the picture: case-by-case approval of each individual GM food, the comprehensive submission dossier, the weight given to prior assessments made in other jurisdictions, the conventional-counterpart baseline and the traceability records that link an ingredient back to its approval.\u003c\/p\u003e\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eThreshold determination — the one per cent per-ingredient limit, its second limb and how GM content is established\u003c\/li\u003e\n\u003cli\u003eDestination control — the boundaries between food, feed and planting uses and the rules that keep them apart\u003c\/li\u003e\n\u003cli\u003eConsignment documentation — approvals, the consignment register and the certified document\u003c\/li\u003e\n\u003cli\u003eMarket entry for processed products — nutritional equivalence and transferred-allergen identification\u003c\/li\u003e\n\u003cli\u003eCase-by-case risk assessment — the submission dossier and the conventional-counterpart comparison\u003c\/li\u003e\n\u003cli\u003eRecognition of prior assessments carried out by other competent authorities\u003c\/li\u003e\n\u003cli\u003eTraceability — the chain records that tie a GM ingredient to its approval\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eWho it's for\u003c\/h2\u003e\u003cp\u003eFood and feed importers, biotechnology and regulatory affairs specialists, customs and border control laboratories, and competent authorities standing up or auditing a GM approval and traceability regime. It earns its place when a shipment is held pending proof of GM status, or when an authority must set out how it approves, registers and traces modified products in editable working text.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56792712479060,"sku":"AGS-04-019","price":490.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/AGS-04-005_05_Genetically_Modified_Foods.png?v=1786639546","url":"https:\/\/agskits.com\/products\/ags-international-technical-guidelines-pack-genetically-modified-foods-regulatio","provider":"Apex Global Solutions","version":"1.0","type":"link"}