The Big Freeze – Transition Period
In the world of Biocidal Product Regulation (BPR), the transition period is a crucial time of change. This period, typically 18 months, occurs between the approval of an Active Substance and the date that approval officially takes effect. Here’s what it means for the market:
- Products Must Be Notified:
Only biocidal products notified during this period can remain on the market. Companies must submit complete registration dossiers for these products to ensure compliance.
- Non-Compliant Products Will Be Removed:
Biocidal products that are not BPR-approved by the end of the transition period will be removed from the market. This emphasises the importance of early notification and preparation.
- No New Market Entries:
During this transition, new products cannot be added to the market. Companies must wait until the transition period concludes and the Active Substance becomes fully approved.
- Brand Registration is Mandatory:
All biocidal product brand names must be registered with the relevant Competent Authority before they can legally be marketed.
The Big Freeze is a pivotal phase that ensures products meet the stringent safety and efficacy standards of BPR. Stay proactive—prepare your notifications, submit your dossiers, and ensure your products are ready for the market when the freeze ends.
Simplified Authorisation – A Smarter Path Under BPR
Simplified Authorisation under the Biocidal Products Regulation (BPR) is an attractive option for companies looking to bring products to market more quickly and cost-effectively. It’s designed for biocidal products that use safer, lower-risk active substances, which are less hazardous to both human health and the environment.
Why Choose Simplified Authorisation?
- Easier Dossier Preparation: Since the materials are inherently safer, the regulatory dossier is simpler and faster to compile.
- Lower Costs: The reduced complexity of the process often translates into significant cost savings.
- Eco-Friendly Focus: The BPR actively promotes this route to support substances with better ecotoxicological profiles, encouraging the industry to move towards greener solutions.
While the benefits are clear, the end product must not require personal protective equipment (PPE).
This restriction makes Simplified Authorisation a more challenging pathway for some formulations but provides a strong incentive to develop safer, sustainable alternatives.
By leveraging this route, businesses can innovate with a focus on safety and sustainability while saving time and resources—helping to shape the future of greener biocidal solutions.
Labelling Under Biocidal Product Regulation (BPR)
Labelling under the Biocidal Product Regulation (BPR) is a cornerstone of compliance, safety, and consumer trust. Here’s a comprehensive breakdown of the requirements:
Active Substance Details:(BPR)
- The label must list the active substance(s) along with their amount in grams per 100 grams.
Dilution Instructions for Concentrates:
- Clear instructions must be provided for dilutions, reflecting the product’s efficacy claims.
Contact Times:
- The label must state the contact time required for the product to achieve its claimed efficacy. This is critical for ensuring proper disinfection and safety.
Expiration Date:
- Labels must include the expiration date or shelf life of the product. This ensures that users are aware of the timeframe during which the product remains effective.
Manufacturer or Supplier Details:
- The label must include the name and full address of the company responsible for placing the product on the market.
BPR Authorisation Number:
- The product must display its unique authorisation number, confirming compliance with BPR regulations.
Intended Use and Application:
- The label must define the intended use and provide detailed application instructions.
Risk Mitigation Measures:
- Information such as personal protective equipment (PPE) requirements, safe handling, storage, and disposal instructions must be included.
## <span style=“color: #DC467D;”>CLP Compliance:
Labels must comply with the Classification, Labelling and Packaging (CLP) Regulation, which includes:
- Hazard pictograms
- Signal words
- Hazard and precautionary statements
Language and Legibility:
- All information must be in the official language(s) of the market and presented in a clear, legible, and durable format.
A Word to Consumers:
Labelling matters. When purchasing biocidal products, always examine the label for:
- Active substances with specified amounts
- BPR authorisation number
- Expiration date
- Clear usage instructions, including contact times
If a product’s label fails to meet these standards, ask yourself: Can I trust its efficacy? Is this the product I want to use for disinfecting an area of concern?
For instance, a product with an approved active substance but missing a BPR authorisation number or expiration date might not be reliable. Personally, I wouldn’t trust such a product.
Getting labelling right is not just about regulatory compliance—it’s essential for building credibility and ensuring consumer confidence in the product’s safety and efficacy.
