The winning weapon that distinguishes Eurochem Ricerche is the availability and the passion that his team has to manage, analyze and solve problems related to its customers. Knowing how to use the interpretation of analytical results, putting them in correlation with the product and with the various production problems gives the added value that often makes the difference in solving problems.

Areas of expertise and market sectors that Eurochem Ricerche is able to address are: Cosmetic, Medical Devices, Medical Deans – Surgical, the detergents and Nutritional Supplements. Considerable importance must be given also to the experience that in many years Eurochem Ricerche has invested in research and characterization of the extracts of vegetable origin and in all those of natural origin used in the various sectors.

Eurochem Ricerche is able to realize the P.I.F. (Product Information File) cosmetics, in accordance with Regulation 1223/2009 of the European Parliament, Annex I.

Very important is the help that the Company may provide for the evaluation of dangerous preparations with the implementation of Technical Data Sheets and Safety Data Sheets as well as a wide range of analytical tests to assess the Flash Point (impact, corrosivity tests in vitro … .).

Eurochem Ricerche performs regularly with interlaboratory tests for the verification of analytical procedures, participate in working groups for the development of new analytical methods, is also certified according to the criteria of ISO 9001: 2008, it is a partner and member of UNIPRO UNI. He has started the procedures for the GLP laboratory accreditation at the Ministry of Health. All staff are subject to a careful and planned training plan and update.

We are looking for volunteers to run tests for evaluating the efficacy and tolerability of cosmetic products.

Our consultancy

Starting from the consultation of the most important databases in the industry, advice on cosmetic products passes through the execution of the basic analysis on raw materials, prototypes and finished products, reaching up to the realization of the final formulation with the start of production of the pilot test. It also provided advice on legislation for all matters relating to the production and marketing of cosmetic products, including the realization of the complete cosmetic dossier of toxicological evaluation and safety in accordance with Regulation no. 1223/2009.

Medical Devices belong to a complex area, which is a large variety of products and is rigidly governed by a legal point of view. It is regulated by Directive 93/42 / EEC and Legislative Decree 46/97 transposition in Italy that manages the classification, the activities of production and marketing.

With the experience gained, to a constant update on the current regulations and to a multidisciplinary team, Eurochem Ricerche provides a useful support in the phase of study, management and certification of medical devices, serving as a consultant to address the various problems and as a laboratory chemical physical and microbiological support.

Using up to date methods and software officers Eurochem Ricerche is able to support the investigation qualitative manufacturers of the product and the market leader, also realizing the hazard assessments required for the correct labeling of products

A food supplement is a substance designed to provide nutrients such as vitamins, minerals, fatty acids or amino acids, that are missing or are not consumed in sufficient quantity in a person’s diet. They should be consumed within safe limits (upper safe level: UL), taking into account the RDA (recommended dietary allowances) and specialists’ recommendations.

To ensure the safety of the product, especially important for based herbal supplements, the following routine tests are required:

· Heavy metals;
· Pesticides;
· IPA;
· Mycotoxins;
· Micribiologiche Analysis.

Class Medical-Surgical belong disinfectants and substances placed on the market as germicides or bactericides, insecticides for domestic and civil use and insect repellents. These products must follow a consent procedure for the production and marketing authorization according to a law that has evolved over the years.