MODULE A1- Internal Production Control  and Inspected Product Testing
  1. Internal audit of the production process and testing of the EU fertilization product under supervision indicates that the manufacturer has fully fulfilled the duties and responsibilities listed in the second, third, fourth and fifth paragraphs, ensured under its own initiative that the product complies with the standards required by the technical regulations, and that this It is a conformity assessment procedure in which conformity is officially declared.
  2. The manufacturer creates a technical file containing the necessary risk analyzes and assessments to determine that the EU fertilization product complies with the relevant legislation. This file is directly related to the conformity assessment of the product and details the design, manufacturing process and functionality of the product. In each case, the technical file contains at least the following information:
    a) a comprehensive description of the EU fertilization product and a description of its intended use corresponding to its declared function,
    b) EU fertilization product concept design, a list of component materials used, information on manufacturing processes,
    c) Declaration of conformity of the EU fertilization product,
    d) Drawings, diagrams and explanations necessary to understand the manufacturing process of the EU fertilization product,
    d) A sample label or brochure containing the required information,
    e) In the case of partially applied harmonized standards or common specifications, technical documents apply sections,
    f) technical and administrative evidence showing that the EU fertilization product complies with the application procedures or adopted national measures, if it contains by-products;
    g) results of calculations made, examinations carried out, etc.
    h) test reports, including reports on product checks for oil retention and explosion resistance,
  3. I) Documents showing that the EU fertilization product complies with the adopted national measures, as well as technical and administrative evidence showing that they comply with the criteria established by the authorized actions,
    i) Names and addresses of the sites and site operators where the EU fertilization product and its main components are produced
  4. The manufacturer carries out all necessary measures throughout the production process and the supervision of this process in order to guarantee compliance of the produced EU fertilization product with the previously specified technical dossier content and the relevant conditions of the technical legislation.
  5. One or more elements of each manufactured product are subjected to one or more tests by the manufacturer or by a different organization on its behalf in order to verify its compliance with the relevant rules of the technical legislation. These tests are carried out by an in-house accredited unit or under the responsibility of a notified body determined by the manufacturer, at the choice of the manufacturer. In cases where the tests are carried out by a notified body, the manufacturer puts the identity registration number of this organization on the product during the production stage, under the responsibility of this organization.
  6. The manufacturer follows these steps:
    The manufacturer shall affix the CE marking on each individual packaging of each EU fertilizer product that meets the requirements of the relevant technical legislation or, if supplied unpackaged, in a document accompanying the EU fertilizer product.
    The manufacturer issues a written EU declaration of conformity for an EU fertilizer product or type and makes it available to national authorities together with technical documentation for 5 years after the EU fertilizer product is placed on the market.
    c) A copy of the EU declaration of conformity should be available upon request from the relevant authorities.
  7. The obligations of the manufacturer specified under the fourth article can be fulfilled by its authorized representative. For this purpose, the authorized representative must be specified in the authorization document, acting on behalf and under the responsibility of the manufacturer.

About Our Company

Certtrace Belgelendirme Eğitim Denetim Muayene Hiz. Ltd. Şti, akademik, belgelendirme ve doğrulama hizmetleri sunan öncü bir kuruluştur.