{"id":2322,"date":"2019-02-06T12:18:07","date_gmt":"2019-02-06T11:18:07","guid":{"rendered":"http:\/\/weekly.uhm.org.mt\/?post_type=article&#038;p=2322"},"modified":"2019-02-06T12:18:07","modified_gmt":"2019-02-06T11:18:07","slug":"procedura-ta-awtorizzazzjoni-mill-ue-ghall-pesticidi","status":"publish","type":"article","link":"http:\/\/weekly.uhm.org.mt\/en\/article\/procedura-ta-awtorizzazzjoni-mill-ue-ghall-pesticidi\/","title":{"rendered":"EU authorisation procedure for pesticides"},"content":{"rendered":"<p><img decoding=\"async\" loading=\"lazy\" class=\"alignnone size-full wp-image-2319\" src=\"http:\/\/weekly.uhm.org.mt\/wp-content\/uploads\/2019\/02\/iStock-943797780-min.jpg\" alt=\"\" width=\"2119\" height=\"1414\" srcset=\"http:\/\/weekly.uhm.org.mt\/wp-content\/uploads\/2019\/02\/iStock-943797780-min.jpg 2119w, http:\/\/weekly.uhm.org.mt\/wp-content\/uploads\/2019\/02\/iStock-943797780-min-300x200.jpg 300w, http:\/\/weekly.uhm.org.mt\/wp-content\/uploads\/2019\/02\/iStock-943797780-min-768x512.jpg 768w, http:\/\/weekly.uhm.org.mt\/wp-content\/uploads\/2019\/02\/iStock-943797780-min-1024x683.jpg 1024w, http:\/\/weekly.uhm.org.mt\/wp-content\/uploads\/2019\/02\/iStock-943797780-min-480x320.jpg 480w\" sizes=\"(max-width: 2119px) 100vw, 2119px\" \/><\/p>\n<p>&nbsp;<\/p>\n<p>In the wake of controversy over the renewal of the approval of glyphosate, the European Parliament set up in February 2018 a special committee on the Union&#8217;s\u00a0authorisation\u00a0procedure for pesticides.\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:360}\">\u00a0<\/span><\/p>\n<p>The 2009 regulation on plant protection products, often referred to as &#8216;pesticides&#8217;, is designed to ensure a high level of protection for human health and the environment, and to enhance the functioning of the internal market while improving agricultural production. Plant protection products are subject to a dual approval process. First, active substances are approved at EU level provided they meet\u00a0a number of\u00a0criteria.\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:360}\">\u00a0<\/span><\/p>\n<p>The Commission approves an active substance for one or more specific uses after a risk assessment by national regulatory agencies and the European Food Safety Authority (EFSA), a risk management exercise by the Commission, and endorsement by a standing committee of Member State representatives.\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:360}\">\u00a0<\/span><\/p>\n<p>Approval may be subject to\u00a0conditions, and\u00a0is typically granted for ten years.\u00a0A number of\u00a0derogations are applicable in specific cases. Second, a commercial plant protection product containing one or more approved active substances is\u00a0authorised\u00a0at Member State level if it satisfies certain conditions, including that it is sufficiently effective in realistic conditions of use; it does not have any (direct or indirect) harmful effects on humans or animals; and it does not have any unacceptable impact on the environment.\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:360}\">\u00a0<\/span><\/p>\n<p>The report sets out a number of recommendations, including: improving transparency (including public access to evaluation studies) and avoiding conflicts of interest; allocating sufficient resources and appropriate expertise to public bodies involved; no longer allowing the use of plant protection products in public spaces; introducing a post-market vigilance system to systematically monitor real-life impacts, including in the long term; funding independent research on effects of and alternatives to pesticides; and improving the functioning of the zonal system.\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:360}\">\u00a0<\/span><\/p>\n<p>The report also calls on the Commission to submit a legislative proposal amending the regulation in order to enable a fast-track approval process\u00a0for low-risk pesticides of biological origin, and to designate Member States carrying out the risk assessment for new applications (as is currently the case for renewals).\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:360}\">\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&nbsp; In the wake of controversy over the renewal of the approval of glyphosate, the European Parliament set up in February 2018 a special committee on the Union&#8217;s\u00a0authorisation\u00a0procedure for pesticides.\u00a0\u00a0 [&hellip;]<\/p>\n","protected":false},"author":7,"featured_media":2319,"menu_order":0,"comment_status":"open","ping_status":"open","template":"","format":"standard","meta":{"_mi_skip_tracking":false,"spay_email":""},"issuem_issue":[96],"issuem_issue_categories":[8],"issuem_issue_tags":[],"translation":{"provider":"WPGlobus","version":"2.8.8","language":"en","enabled_languages":["mt","en"],"languages":{"mt":{"title":true,"content":true,"excerpt":false},"en":{"title":true,"content":true,"excerpt":false}}},"_links":{"self":[{"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/article\/2322"}],"collection":[{"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/article"}],"about":[{"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/types\/article"}],"author":[{"embeddable":true,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/users\/7"}],"replies":[{"embeddable":true,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/comments?post=2322"}],"version-history":[{"count":2,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/article\/2322\/revisions"}],"predecessor-version":[{"id":2324,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/article\/2322\/revisions\/2324"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/media\/2319"}],"wp:attachment":[{"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/media?parent=2322"}],"wp:term":[{"taxonomy":"issuem_issue","embeddable":true,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/issuem_issue?post=2322"},{"taxonomy":"issuem_issue_categories","embeddable":true,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/issuem_issue_categories?post=2322"},{"taxonomy":"issuem_issue_tags","embeddable":true,"href":"http:\/\/weekly.uhm.org.mt\/en\/wp-json\/wp\/v2\/issuem_issue_tags?post=2322"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}