Renolab is a laboratory certified by the Italian Ministry of Health for analyses and studies carried out in accordance with the principles of Good Laboratory Practices (GLP).
Renolab has always specialised in chemical determination analyses on agrochemicals and over the years it has extended its experience into other major chemical sectors: biocides and medicinal products, cosmetics, nutraceutical products, herbal medicines and diet supplements, pharmaceutical and veterinary products, additives, plastics, fertilisers and biostimulants.It also started a specialised area of microbiological studies.
Chemical and physical characterisation, 5-Batch Analysis, GLP Residue Studies and GLP Microbiological Studies. Study plans and reports are drawn up in accordance with the principles and guidelines of GLP, following the standard procedures, with the aim of meeting the customer’s specific needs.
Biocompatibility Evaluation of Medical Devices
Biocompatibility evaluation is a fundamental process in the development and certification of medical devices. It involves assessing the biological response generated by the device’s contact with cells, tissues, or body fluids, with the aim of preventing adverse effects and ensuring patient safety. The topic was addressed by Matteo Calassanzio, Head of the Microbiology Department at
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New Accredited Tests for the Biological Evaluation of Medical Devices
Renolab expands its portfolio of accredited services with two new in vitro tests for the biological evaluation of medical devices in accordance with the ISO 10993 series, essential for demonstrating biological safety and supporting the CE marking process. Consult our ACCREDIA accreditation certificate and the list of accredited tests. In Vitro Cytotoxicity – XTT Test
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Ethanol under review: potential impact on EU disinfectant industry
The European Chemicals Agency (ECHA) is reviewing ethanol for potential exclusion from biocidal products (disinfectants), with a potential classification as carcinogenic and reprotoxic. This review could significantly restrict or exclude ethanol use in disinfectants across the EU. A public consultation is ongoing to gather evidence and identify alternatives. Ethanol remains one of the most effective
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The 14th issue of T-Magazine is out!
This December marks the release of the 14th edition of the Tentamus Italia Group’s magazine: an issue that closes the year with technical insights and perspectives that blend analysis, research, and… a touch of festive content. In this edition, you can dive into topics such as: 🥚Colour and perception: the invisible language of food 🐄
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Renolab to Speak at the Regulatory Dossier Manager Deep Dive Day Organized by INT.E.G.RA.
On November 5, 2025, we will participate as guest speakers at the Regulatory Dossier Manager Deep Dive Day, a professional training event organized by INT.E.G.RA. at the Hotel Due Mari – Training Center in Sestri Levante (GE), Italy. Gianluca Scarlino, Quality Assurance Manager at Renolab, will give a presentation titled: “GLP: From Theory to Practice
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In Vitro Testing for Cosmetics
In Vitro Testing for Cosmetics: Alternative Methods for Product Safety (Reg. 1223/2009) Cosmetic products marketed in Europe must comply with Regulation (EC) No. 1223/2009, which prohibits animal testing and requires the use of validated alternative methods, such as in vitro testing. What the European Cosmetic Regulation Requires Regulation 1223/2009 mandates a human safety assessment of
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