Quality & Regulatory Compliance
European manufacturing, ISO 22716, controls at every step
Every LissCréation product is manufactured in Europe under ISO 22716 (Good Manufacturing Practices), controlled at each production step, documented in a Product Information File (PIF) and notified to the CPNP portal before being placed on the market. Every batch is traceable, from raw material to delivered bottle.
The 7 pillars of our quality approach
European manufacturing
Production carried out within the European Union, under EU regulatory framework, with audited and documented raw material suppliers.
ISO 22716 standard (GMP)
Our processes follow ISO 22716, the international reference for cosmetic Good Manufacturing Practices: premises, personnel, equipment, production, control, documentation.
Quality controls at every step
Incoming raw material control, in-process checks (pH, viscosity, density, appearance, odour), microbiological testing and finished product validation before release.
EU Cosmetics Regulation compliance
Compliance with Regulation (EC) No 1223/2009: authorised ingredients, maximum concentrations, INCI labelling, substantiated claims, designated Responsible Person.
Product Information File (PIF)
Each reference has a complete PIF: quantitative formula, specifications, manufacturing method, stability and compatibility testing, safety report signed by a toxicologist.
CPNP notification before market launch
No product is sold without prior notification to the European Commission's Cosmetic Products Notification Portal — a mandatory condition for placing a product on the EU market.
Batch traceability
Unique batch number on every unit, archived batch records and retained samples: we can trace back within minutes to the raw material, the manufacturing date and the customer served.
What we control and document
From raw material sourcing to finished batch release
Our quality at a glance
ISO
22716 — cosmetic GMP
1223/2009
EU regulation applied
100%
of batches traced and archived
CPNP
notified before sale
FAQ — Quality & compliance
What does the ISO 22716 standard mean?
ISO 22716 is the international standard for Good Manufacturing Practices (GMP) applied to cosmetics. It covers premises, personnel, equipment, production, quality controls, documentation and deviation management. EU Regulation (EC) 1223/2009 requires cosmetics to be manufactured in compliance with GMP.
What is the Product Information File (PIF)?
The PIF is the mandatory dossier kept available to authorities for 10 years after the last placing on the market. It contains the product description, quantitative formula, raw material specifications, manufacturing method, evidence for claimed effects and the safety report signed by a qualified assessor.
What is CPNP notification?
The CPNP (Cosmetic Products Notification Portal) is the European Commission portal on which every cosmetic product must be notified before being placed on the EU market. The notification informs authorities and poison centres of the product composition. We handle this for our clients.
How does batch traceability work?
Each production run receives a batch number printed on the unit. This number links the product to its batch record: raw materials used with their certificates of analysis, operators, equipment, control results, manufacturing date, quantities and recipients. Retained samples are kept.
Who is the Responsible Person for my products?
EU regulation requires a Responsible Person established in the EU for each product. If your brand has a European entity, it can take this role; otherwise we can act as Responsible Person (Article 4 of Regulation EC 1223/2009).
Are your products tested on animals?
No. Animal testing is banned in the European Union for cosmetic products and their ingredients. Safety is established through documentary toxicological assessment and validated alternative methods.
Can I obtain the quality documentation for my products?
Yes. For each reference ordered we provide the technical data sheet, INCI list, batch certificate of analysis and proof of CPNP notification. The PIF remains available on request within the regulatory framework.