Gain insight into the EU BPR and learn how to comply with this regulation
This interactive course will be delivered in-person over three days at Health Innovation Centre of Lancaster University, UK. 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.
The course will include practical exercises to familiarise yourself with IUCLID6, R4BP and the SPC editor. The workshop will cover all the main aspects of those tools and give you the chance to become familiar with the software and how it can be used most effectively. The workshop is delivered by experienced IUCLID 6 trainers and all sessions are recorded for attendees to review, at their convenience, if they wish to revisit topics.At a glance
Here is a summary of what you can expect from this course.
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3 full day in-person classroom sessions
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A copy of our Intro to BPR course manual
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Practical exercises to put your knowledge into practice
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Interaction with our experienced BPR experts
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All for EUR 1875 (including applicable sales taxes)
Topics to be Covered in this Classroom
- Core Principles of EU Biocides Regulation
- Active Substance Approval
- BPR Transitional Period
- Article 95: Approved Supplier List
- Treated Articles
- Brexit and UK-BPR
- Borderline Products
- Product Authorisation Routes
- Product Families
- Data Requirements for Product Authorisation
- Introduction to BPR IT Tools
Who Should Attend?
This course has been specifically developed to introduce you to the EU Biocidal Products Regulations. It will be most relevant to:
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Those responsible for preparing and submitting biocidal product authorisations
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Manufacturers and formulators of biocidal products and articles treated with biocidal products
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Importers of biocidal products and articles treated with biocidal products
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Anyone interested in understanding the EU BPR
Learning Outcomes
This 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 products 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.
Instructors
Join our leading scientific and regulatory experts in this in-person course
Dr Aiden Robertson
Senior Chemistry Consultant
Dr Hayley Lewis
Senior Regulatory Consultant
Dr Emma Miller
Chemistry Consultant