The Biocidal Products Regulation (BPR) introduced the concept of a "Biocidal Product Family" which allows for the grouping of biocidal products with similar compositions and intended functions. During this course, you will learn what a biocidal product family is and why it can be beneficial for businesses to make use of this regulatory tool to reduce regulatory burden.
This course will also provide information on how to determine what products can and cannot be grouped into a biocidal product family, and how extensions and subsets can be used to expand the definition of the family. The aim of this course is to provide you with the tools required to identify where your products may be combined into a product family to reduce the regulatory costs to place those products on the market .
Highlights
Here is a summary of what you can expect from this online course:
-
7 course modules
-
Instant access to 1.5 hours of course recordings
-
Summary handouts and additional resources
-
Test your learning with practical quizzes and exercises
-
Complete the course in approximately 2.5 hours
-
Completion certificate
-
All for EUR 395 including applicable taxes
Topics covered in this e-Learning course
- What is a biocidal product family?
- What products can be included?
- Defining the core dossier and advising on the inclusion of subsets and extensions
- Understanding the benefits of the BPF when generating endpoint data as well as giving an overview of what data is required for the dossier.
- Discussing risk assessment for a BPF differences with biocidal product dossier
- Differences in the Product Assessment Report and IUCLID dossier for BPFs
- What happens after the dossier is submitted?
Course curriculum
-
1
Welcome to this course
-
Welcome
-
How to use this course
-
Introduction to Biocidal Product Families
-
Introduction - Handout
-
Before we begin...
-
-
2
Module 1 - What is a Biocidal Product Family?
-
Introduction to Module 1
-
Module 1 - What is a Biocidal Product Family?
-
Module 1 - Handout
-
Module 1 - Test your knowledge
-
-
3
Module 2 - Identifying Product Family Formulations
-
Introduction to Module 2
-
Module 2 - Identifying Product Family Formulations
-
Module 2 - Handout
-
Module 2 - Practical Exercise
-
Module 2 - Exercise Solutions
-
Module 2 - Test your knowledge
-
-
4
Module 3 - Building the Core Dossier
-
Introduction to Module 3
-
Module 3 - Building the Core Dossier
-
Module 3 - Handout
-
Module 3 - Practical Exercise
-
Module 3 - Exercise Solutions
-
Module 3 - Test your knowledge
-
-
5
Module 4 - Expanding the Core Dossier
-
Introduction to Module 4
-
Module 4 - Expanding the Core Dossier
-
Module 4 - Handout
-
Module 4 - Practical Exercise
-
Module 4 - Execise Solutions
-
Module 4 - Test your knowledge
-
-
6
Module 5 - Endpoint Data
-
Introduction to Module 5
-
Module 5 - Endpoint Data
-
Module 5 - Handout
-
Module 5 - Test your knowledge
-
-
7
Module 6 - Dossier Preparation
-
Introduction to Module 6
-
Module 6 - Dossier Preparation
-
Module 6 - Handout
-
Module 6 - Test your knowledge
-
-
8
Module 7 - Post-submission
-
Introduction to Module 7
-
Module 7 - Post-submission
-
Module 7 - Handout
-
Module 7 - Test your knowledge
-
-
9
Congratulations! Here's what's next
-
You're almost done!
-
Before you go...
-
Learning Outcomes
At the end of the course, participants will be able to:
- Describe what a biocidal product family is and how it can be used to the benefit of businesses and authorities
- Understand the potential differences between a Biocidal Product Family assessment and those of single Biocidal Products
- Demonstrate what products can and cannot be included in a Biocidal Product Family through work examples and activities to identify the backbone composition
- Understand what is the "core" dossier and the difference between "subsets" and "extensions" and where these can and cannot be used
- Identify what endpoint data is and what information is required for the Risk Assessment for the core dossier and any subsets or extensions
- Develop some understanding of the format for the submission dossier and the evaluation process
Who should attend?
-
Manufacturers or distributors of biocidal products who have mutliple products with similar compositions and intended functions
-
Anyone considering the preparation and submission of a Biocidal Product Family dossier
Instructor(s)

Adam Thickett
Regulatory Consultant