Our nano analyses comply with the most demanding international standards and guidelines.
From sub-nanometer size resolution to surface reactivity and regulatory compliance assessment, our instrumentation covers the full physicochemical characterization of engineered nanomaterials.
Method — 01Comprehensive nanoparticle size characterization, including particle counting and size distribution, using SEM, DLS, and laser granulometry. Assessment of dispersion stability and nano-emulsion behavior over time (aggregation, sedimentation, size evolution).
Method — 02High-resolution imaging of particle shape, aggregation state, crystallinity and internal structure using SEM-EDS. Advanced surface and structural analysis using complementary techniques such as TOF-SIMS.
Method — 03Specific surface area (BET), pore size distribution, pore volume and micropore analysis by gas adsorption. Volume specific surface area (VSSA) and density measurement by helium pycnometry.
Method — 04Elemental analysis, trace metal quantification and chemical purity assessment for nanoparticle batches and nano-enabled formulations. Advanced characterization with GC-MS, LC-MS/MS, HR-MS, NMR for complex matrices.
Method — 05Zeta potential, surface functionalization, oxidation state and chemical bonding analysis, essential for colloidal stability and biocompatibility assessment. Surface-sensitive analysis using TOF-SIMS and advanced interfacial techniques.
Method — 06Phase identification, crystallite size, crystallinity degree and lattice parameter determination for nanopowders and thin films.
Method — 07Thermal stability, optical absorption and photoluminescence characterization for quantum dots, plasmonic nanoparticles and nano-enabled coatings.
Method — 08Detection and quantification of nanoparticles in complex matrices (liquids, solids, biological and environmental samples) using ICP-MS/MS. Critical for trace-level analysis, regulatory compliance, and environmental or health risk assessment.
Method — 09Compliance-ready from day one. Support for REACH, R-nano declaration, cosmetic regulation (EC 1223/2009), food regulation (INCO 1169/2011), EFSA and ANSES guidelines. Development, validation and transfer of analytical methods tailored to nanomaterials.
Method — 10Support in the development of nano-enabled products, including formulation optimization and performance evaluation. Identification of safer or compliant alternatives to chemical substances (substitution strategy).
Nanomaterials face strict and evolving regulatory requirements. Our tests are designed to directly feed your dossiers.
| Framework | Scope & FILAB support |
|---|---|
| REACH | Registration dossier support for nanomaterials (ENMs): physicochemical characterization, particle size distribution, surface properties, dissolution, dispersion stability, in line with Annex VI–XI requirements. |
| EU NanoReg / ECHA guidance | Nano-specific characterization aligned with ECHA guidance: size, morphology, surface chemistry, and dispersion behavior to support regulatory submissions. |
| OECD Test Guidelines | Physicochemical testing according to OECD guidelines: OECD 105 (water solubility), OECD 120 (solution/extraction behavior), OECD 125 (particle size distribution), OECD 318 (dispersion stability in environmental media). |
| Cosmetics (EC 1223/2009) | Support for nanomaterial notification dossiers: particle size, morphology, surface characteristics, chemical composition and purity, in line with SCCS expectations. |
| Food / FCM (EC 10/2011) | Characterization of nanomaterials used in food contact materials: size distribution, chemical composition, migration-related data, with support for EFSA submissions. |
| MDR / IVDR (EU 2017/745) | Material characterization for medical devices containing nanomaterials: surface properties, chemical composition, particle size, supporting biocompatibility assessment (ISO 10993 framework). |
| R-nano (France) | Preparation of data required for mandatory annual declaration of nanomaterials, including physicochemical properties and tonnage-related information. |
All results legally valid for regulators, customers and authorities.
Reports structured in formats directly usable for REACH, EFSA or MDR submissions — saving your team weeks of reformatting.
Our specialists advise on the right test selection for your regulatory pathway, avoiding costly gaps or unnecessary testing.
Filab serves R&D teams, quality managers and regulatory affairs departments across all sectors where engineered nanomaterials are developed or used.
Liposomes, polymeric nanoparticles, drug delivery systems. Size, surface charge and stability for regulatory submissions.
Electrode nanomaterials, cathode powders, electrolyte additives. BET surface, XRD phase, particle size and morphology.
Quantum dots, conductive inks, dielectric nanolayers. Optical properties, chemical purity and morphology characterization.
TiO₂, ZnO, silver NPs for UV filters and antimicrobials. EU cosmetics regulation notification dossier support.
Nano-silica, nano-TiO₂ in cement and paints. Surface area, dispersibility and durability testing for functional coatings.
Nano-reinforced composites, surface coatings, lubricant additives. Mechanical, thermal and chemical characterization.
Catalyst nanoparticles, zeolites, supported metals. BET, XRD, chemisorption and active site quantification.
From sample to report
Fill the form with your nanomaterial type, analytical need and deadline. Our nano specialists review your brief the same day.
We send a tailored test plan with method selection, standards and pricing adapted to your regulatory context and budget.
Ship your samples securely. We handle all conditioning and nano-specific preparation protocols upon arrival.
Testing conducted on state-of-the-art instruments by certified analysts, with full ISO 17025 traceability and QA documentation.
Detailed accredited report with data, interpretation, conclusions and regulatory context — delivered digitally in 5 days or 48h express.
Expertise where scale demands precision
We support R&D, regulatory and quality teams developing or using engineered nanomaterials — from early formulation to dossier submission.
Accreditation. Every nano result is traceable, accredited and accepted by regulators worldwide.
Speed. Standard 5-day turnaround. 48h express service for time-critical regulatory or production decisions.
Expertise. A dedicated team focused exclusively on nanomaterial characterization and regulation.
From early-stage startups to global manufacturers, our clients rely on Filab for critical nanomaterial characterization decisions.
"Filab characterized our nano-silica grades with DLS, BET and TEM in a single accredited package. Saved us weeks of dossier preparation for REACH."
"Their nano team delivered a complete EC 1223/2009 notification dossier on our TiO₂ filter — particle size, morphology, surface chemistry — all SCCS-ready."
"We rely on Filab for BET surface, XRD phase and ICP-MS purity on every cathode powder batch. Reports go straight to our automotive customers."
Request your nanomaterials testing quote today
From account management to technical video debriefings, our entire nano team communicates fluently in English.
All CoAs and analytical reports are delivered in scientific English, fully compliant with international standards (REACH, EFSA, FDA, ICH, SCCS).
Use your preferred courier (FedEx, DHL, UPS...). We provide a dedicated customs guide and notify you upon sample arrival.
