This virtual classroom introduces you to the core principles and main features of current biocidal legislation in the EU. During this course, you will learn how your product is affected by the BPR and what you need to do to be compliant if you have a biocidal product or a treated article. The trainer will cover the terminology used, timelines and the potential costs, enabling you to make the right decisions for your business. This course will introduce the options available for getting your biocidal product authorised in the EU. Additionally, we will cover the types of product authorisation, including costs and data requirements, to give you the information you need to decide how to move forward for your company.
Dates and Time
November 9, 10, 16, 17, 23 & December 1 (9:30am-2:00pm GMT)
Learning Outcomes
This virtual classroom will answer the following questions:
What is the BPR?
What is the difference between a Biocidal Product and a Treated Article?
Does it affect me?
What are my obligations and how do I meet them?
Product Authorisation Basic: Who, what and when?
What IT tools can I use for Product Authorisation?
What is happening with Brexit and BPR regulations in the UK?
At the end of the course, participants will be able to:
Define whether they have a biocidal product or a treated article
Understand the different types of biocidal product authorisations
Assess your products and establish your obligations under BPR
Identify data requirements and costs associated with the preparation of a product authorisation
Understand how to prepare and submit a biocidal product authorisation dossier using IT tools Identify the IUCLID 6, SPC editor and R4BP functionalities required to prepare and submit a dossier;
Prepare endpoint summaries in IUCLID6 to fulfil the requirements for product authorisation;
Understand how to use IUCLID6, SPC editor and R4BP to prepare and submit your product authorisation.
Price
€1.095,00