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Analytical instrumentation

Analytical Instrumentation

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ICP-OES (Inductively Coupled Plasma – Optical Emission Spectrometry)

to quantify metal ion at trace level in solution.
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NMR (Nuclear Magnetic Resonance)

to identify and quantify organic compounds.
Paricularly, the research spectrometers Varian Mercury 400 MHz e Bruker Advance 600 MHz will be used.
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QTRAP

a hybrid system that merges triple quadrupole and linear on trap capabilities with high flexibility in scan protocols; it also includes “neutral loss”, “precursor-ion scan” and “multiple reaction monitoring”.

QSTAR

is a hybrid quadrupole / time-of-flight system that supports high resolution and high mass range analysis. It’s also possible to analyze small quantities of sample through nanoelectrospray ionization of the sample itself.
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HPLC-GC (High-Performance Liquid Chromatograph or Gas Chromatograph)

connected to a mass spectrometer to analyze volatile organic compounds (VOCs) and / or compounds in solution; HPLC equipped with a UV-diode array detector (UV-DAD) to analyze organic compounds in solution.

What we do to let a product become TPD2 compliant

in brief

1
GETTING TO KNOW YOUR COMPANY PROFILE AND PRODUCTS:

fulfillment of the dedicated form . Of course after having sign an NDA: you can trust us, but we want to be sure you’ll be. After that, you will receive our quote.

2
SUBMISSION OF SAMPLES TO BE ANALYZED AND PROFILING OF YOUR COMPANY IN THE EU-CEG PORTAL:

we will check that everything’s ok and then we will move forewords; we will get a Submitter ID on behalf of you.

3
TOXICOLOGICAL LITERATURE SEARCH

and issuing of a complete risk assessment report concerning every relevant ingredient of the blend. After that we will set up a testing solution suitable for your needs.

4
ANALYSIS OF THE EMISSIONS

and issuing of an analytical report. Parameters and conditions will be set as function of the type of products and markets.

5
COMPLIANCE

we will check every details to guarantee your product is compliant. If not, we will evaluate together how to proceed to obtain compliance.

6
PRODUCTION OF TECHNICAL DOSSIER.

through the integrated evaluation of information from manufacturer, analytical labs and from toxicological risk assessment.

7
SUBMISSION OF NOTIFICATION.

You will receive the EC-ID and you will be then ready to market your products in the European Union.