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Programme

Timings are in CEST (Copenhagen)

  1. Registration

  2. Requirements for market authorisation under the BPR

    The trainers will take you through the requirements for approval of biocidal products under the BPR that will enable you to distinguish between the pros and cons of the different application procedures.

    Michael Fink Michael Fink
    Vice President, Senior Regulatory Expert, DHI, Denmark
    Jack Frausing Nielsen Jack Frausing Nielsen
    Regulatory Adviser, DHI, Denmark

  3. Refreshment break

  4. Data and documentation requirements

    The trainers will take you through the mandatory elements for an application, including data and documentation requirements and you will learn how to structure the application process.

  5. Lunch

  6. The biocidal product family concept

  7. Legal requirements for endocrine disruptors

  8. Refreshment break

  9. IT Tools

    Instructions on how to use the R4BP 3 (Register for Biocidal Products), IUCLID 6 and SPC Editor programmes. You will also be briefed about the upcoming SPC IUCLID format.

  10. BPR status

    The instructors wrap-up the course with an overview of the status of biocide legislation at national and EU level.

  11. Finish

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