Question 1

What does hygiene products contract filling cost at Avoria GmbH?

Accepted Answer

Costs depend on the product category (disinfectant, cleaning agent, industrial cleaner), the active ingredient and its concentration, the required scope of analysis (GC-MS active determination, CLP classification), the container format and the order quantity. For a reliable calculation we need the product specification or recipe, target volume, planned label claims and desired format. Inquiries are processed on working days.

Question 2

What minimum order quantities apply to hygiene products?

Accepted Answer

MOQs vary by product category, raw material availability and container format. For disinfectants on common active ingredient bases, the typical minimum quantity is 50-200 liters of finished product. For cleaning agents and industrial cleaners: from approx. 100-500 kg depending on formulation complexity and format.

Question 3

Do I need a safety data sheet for my hygiene product?

Accepted Answer

For CLP-classified hygiene products - disinfectants based on alcohol, chlorine or quaternary ammonium, concentrated cleaners, corrosive formulations - an SDS per REACH Art. 31 is mandatory for commercial buyers. Avoria GmbH prepares SDS for produced batches on request.

Question 4

Can virucidal hygiene products be produced at Avoria GmbH?

Accepted Answer

Yes, subject to the regulatory requirements. Virucidal disinfectants are biocidal products of product type 4 (PT4) under BPR 528/2012. The virucidal claim on the label is tied to the EN 14476 approval of the active ingredient used. Avoria GmbH handles production, filling and CLP-compliant documentation - the biocidal product authorization rests with the client as the party placing the product on the market.

Question 5

What does the batch record cover for hygiene products?

Accepted Answer

The batch record documents: analytical incoming result for raw materials (active ingredient, excipients), manufacturing log with batch number, filling date, fill quantity log with tolerance evidence. For biocide-regulated products: CLP classification note, SDS reference, active ingredient concentration result. For ADR-classified products: dangerous goods packaging evidence.

Question 6

How is the active ingredient content controlled in hygiene products filling?

Accepted Answer

Avoria GmbH verifies incoming active-ingredient raw materials via GC-MS identity testing before processing. For finished goods where proof of active content is required on the CoA (e.g. 70% isopropanol concentration in IPA disinfectants), we perform quantitative GC analyses on request.

Question 7

What do clients need to know about the Biocidal Products Regulation (BPR 528/2012)?

Accepted Answer

The BPR 528/2012 governs the placing on the market and authorization of biocidal products in the EU - this includes disinfectants and certain cleaning and protective agents. Avoria GmbH produces as a contract manufacturer - the biocidal product authorization and responsibility for BPR compliance rest with the client as the party placing the product on the market.

Hygiene product filling service – ISO 9001 & HACCP