REGULATORY SUPPORT<\/strong><\/h1><\/div><\/div><\/div><\/div><\/div><\/div>For the compliance of your products, we help you move within the regulatory system that defines the mandatory information field, assisting at all stages of the process.<\/strong><\/h4>\n<\/div><\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nDrafting of documentation<\/span><\/p>\n<\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nMediation with
<\/span>ministerial bodies<\/span><\/p>\n<\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nPersonalized advice<\/span><\/p>\n<\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nCertifications
<\/span>Kosher and Halal<\/span><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>DRAFTING DOCUMENTATION<\/span><\/h2><\/div>![](\"https:\/\/staging-food.trusticert.com\/wp-content\/uploads\/2018\/02\/tile-line.png\" "\\"tile-line\\"")
<\/span><\/div><\/div><\/div><\/div><\/div>The placing of a novel food on the Union market involves the drafting of an application for authorization which must contain the scientific data supporting the substance subject of the request, in accordance with Reg. (EU) 2015\/2283 which entered in force by repealing the previous Reg. (EC) 258\/97.
<\/span>All the burden of data research, analysis and material in favor of the aforementioned substance falls on the distributor or manufacturer in the event that he directly deals with placing the product on the Community market.<\/span><\/p>\nWe take care of drawing up suitable documentation for you and adequately supported by technical and scientific material, allowing you to optimize time and avoid running the risk of submitting a non-compliant application. An application that is not well completed and unsatisfactory from a technical-scientific point of view in fact often involves the rejection or slowdown of a practice with all the consequent loss of costs and time, preventing your company from optimizing the work of selection and research of new products.<\/span><\/p>\nWe also help you evaluate which product to offer on the domestic and foreign market, based on a careful analysis of costs and benefits for the product itself.<\/span><\/p>\n<\/div>REQUEST A QUOTE<\/span><\/a><\/div><\/div><\/div><\/div><\/div><\/div><\/div>MEDIATION WITH MINISTERIAL BODIES<\/span><\/h2><\/div><\/span><\/div><\/div><\/div><\/div><\/div>Interfacing with the reference ministerial bodies is not always easy and requires time and use of internal resources.<\/span><\/p>\nThanks to our skills and consolidated contacts with regulatory bodies, you can save time and costs by identifying the competent body more easily, evaluating whether the specific compliance burden you are dealing with is your responsibility or the manufacturer’s, obtaining opinions, preventive opinions and risk assessments even before submitting the application for the authorization request.<\/span><\/p>\n<\/div>REQUEST A QUOTE<\/span><\/a><\/div><\/div><\/div><\/div><\/div><\/div><\/div>PERSONALIZED CONSULTANCY<\/span><\/p>\n\u00a0<\/span><\/p><\/h2><\/div><\/span><\/div><\/div><\/div><\/div><\/div>Each company has its own internal dynamics and marketing choices dictated by market needs and by the commercial and ethical position it undertakes. For this reason we believe that every reality must be treated with a tailor made consultancy service, based not only on the objective demands of global markets, but also on the way in which you want to grow and promote your company.
<\/span>Through personalized advice we can develop with you the growth of your products in line with the story of those who thought and wanted them, you.<\/span><\/p>\n<\/div>
For the compliance of your products, we help you move within the regulatory system that defines the mandatory information field, assisting at all stages of the process.<\/strong><\/h4>\n<\/div><\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nDrafting of documentation<\/span><\/p>\n<\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nMediation with
<\/span>ministerial bodies<\/span><\/p>\n<\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nPersonalized advice<\/span><\/p>\n<\/div><\/div><\/div><\/i><\/div><\/a><\/div><\/div>\nCertifications
<\/span>Kosher and Halal<\/span><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>DRAFTING DOCUMENTATION<\/span><\/h2><\/div><\/span><\/div><\/div><\/div><\/div><\/div>The placing of a novel food on the Union market involves the drafting of an application for authorization which must contain the scientific data supporting the substance subject of the request, in accordance with Reg. (EU) 2015\/2283 which entered in force by repealing the previous Reg. (EC) 258\/97.
<\/span>All the burden of data research, analysis and material in favor of the aforementioned substance falls on the distributor or manufacturer in the event that he directly deals with placing the product on the Community market.<\/span><\/p>\nWe take care of drawing up suitable documentation for you and adequately supported by technical and scientific material, allowing you to optimize time and avoid running the risk of submitting a non-compliant application. An application that is not well completed and unsatisfactory from a technical-scientific point of view in fact often involves the rejection or slowdown of a practice with all the consequent loss of costs and time, preventing your company from optimizing the work of selection and research of new products.<\/span><\/p>\nWe also help you evaluate which product to offer on the domestic and foreign market, based on a careful analysis of costs and benefits for the product itself.<\/span><\/p>\n<\/div>REQUEST A QUOTE<\/span><\/a><\/div><\/div><\/div><\/div><\/div><\/div><\/div>MEDIATION WITH MINISTERIAL BODIES<\/span><\/h2><\/div><\/span><\/div><\/div><\/div><\/div><\/div>Interfacing with the reference ministerial bodies is not always easy and requires time and use of internal resources.<\/span><\/p>\nThanks to our skills and consolidated contacts with regulatory bodies, you can save time and costs by identifying the competent body more easily, evaluating whether the specific compliance burden you are dealing with is your responsibility or the manufacturer’s, obtaining opinions, preventive opinions and risk assessments even before submitting the application for the authorization request.<\/span><\/p>\n<\/div>REQUEST A QUOTE<\/span><\/a><\/div><\/div><\/div><\/div><\/div><\/div><\/div>PERSONALIZED CONSULTANCY<\/span><\/p>\n\u00a0<\/span><\/p><\/h2><\/div><\/span><\/div><\/div><\/div><\/div><\/div>Each company has its own internal dynamics and marketing choices dictated by market needs and by the commercial and ethical position it undertakes. For this reason we believe that every reality must be treated with a tailor made consultancy service, based not only on the objective demands of global markets, but also on the way in which you want to grow and promote your company.
<\/span>Through personalized advice we can develop with you the growth of your products in line with the story of those who thought and wanted them, you.<\/span><\/p>\n<\/div>
Drafting of documentation<\/span><\/p>\n<\/div><\/div><\/div> Mediation with Personalized advice<\/span><\/p>\n<\/div><\/div><\/div> Certifications The placing of a novel food on the Union market involves the drafting of an application for authorization which must contain the scientific data supporting the substance subject of the request, in accordance with Reg. (EU) 2015\/2283 which entered in force by repealing the previous Reg. (EC) 258\/97. We take care of drawing up suitable documentation for you and adequately supported by technical and scientific material, allowing you to optimize time and avoid running the risk of submitting a non-compliant application. An application that is not well completed and unsatisfactory from a technical-scientific point of view in fact often involves the rejection or slowdown of a practice with all the consequent loss of costs and time, preventing your company from optimizing the work of selection and research of new products.<\/span><\/p>\n We also help you evaluate which product to offer on the domestic and foreign market, based on a careful analysis of costs and benefits for the product itself.<\/span><\/p>\n<\/div> Interfacing with the reference ministerial bodies is not always easy and requires time and use of internal resources.<\/span><\/p>\n Thanks to our skills and consolidated contacts with regulatory bodies, you can save time and costs by identifying the competent body more easily, evaluating whether the specific compliance burden you are dealing with is your responsibility or the manufacturer’s, obtaining opinions, preventive opinions and risk assessments even before submitting the application for the authorization request.<\/span><\/p>\n<\/div> PERSONALIZED CONSULTANCY<\/span><\/p>\n \u00a0<\/span><\/p><\/h2><\/div> Each company has its own internal dynamics and marketing choices dictated by market needs and by the commercial and ethical position it undertakes. For this reason we believe that every reality must be treated with a tailor made consultancy service, based not only on the objective demands of global markets, but also on the way in which you want to grow and promote your company.
<\/span>ministerial bodies<\/span><\/p>\n<\/div><\/div><\/div>
<\/span>Kosher and Halal<\/span><\/p>\n<\/div><\/div><\/div>DRAFTING DOCUMENTATION<\/span><\/h2><\/div>
<\/span><\/div><\/div>
<\/span>All the burden of data research, analysis and material in favor of the aforementioned substance falls on the distributor or manufacturer in the event that he directly deals with placing the product on the Community market.<\/span><\/p>\nMEDIATION WITH MINISTERIAL BODIES<\/span><\/h2><\/div>
<\/span><\/div><\/div><\/span><\/div><\/div>
<\/span>Through personalized advice we can develop with you the growth of your products in line with the story of those who thought and wanted them, you.<\/span><\/p>\n<\/div>