Learning Outcomes
After completing the modules in this eLearning course, you will be able to:
MODULE 1 - Introduction and context of the BPR
- Explain why biocidal products are regulated
- Describe the objectives, scope and basic principles of the Biocidal Products Regulation (BPR)
- Relate the BPR in context of previous biocides legislation and current relevant chemicals legislation
MODULE 2 - Treated articles
- Outline the provisions of the BPR as they apply to treated articles
- Describe the labelling requirements required for certain treated articles
- Recall the obligation for treated article suppliers to respond to certain information requests from consumers
- Recognise the scope issues and relationship between a treated article and a biocidal product
MODULE 3 - Biocides stakeholders
- Identify the key actors in the regulatory processes for the BPR
- Describe the role and responsibilities of regulators, industry and other stakeholders
- Identify what options and opportunities companies have when interacting with regulators
MODULE 4 - Enforcement
- Define the roles of the different stakeholders in the compliance with and the enforcement of the BPR
- Outline the obligations (and the requirements) required of the various stakeholders in enforcement of biocides
- Summarise the role of the ECHA Forum and its subgroups in the co-ordination of enforcement priorities and activities
MODULE 5 - Authorisation routes
- Recall the timeline, main steps and processes for the biocidal active substance review programme
- Outline the various authorisation routes available for biocidal products
- Describe the role and responsibilities of the actors involved in these processes
MODULE 6 - Available guidance
- Recognise that additional resources/tools are available to assist your understanding and compliance with the requirements and obligations of the Biocidal Products Regulation
- Identify the type of guidance you need and where you can find it