Our Certifications
In this section, you will find the Tests, Laboratory Analyses, and Certifications for Salus Thermae products and their characteristics.
Each batch, each new product, is tested and certified for your Safety and Protection.
Salus Thermae by CNT Salus Mundi is a guarantee of scientifically proven Quality.
CERTIFICATIONS AND TESTS RELATED TO OUR ACTIVE INGREDIENT SYNTHAG
Evaluation tests on the inactivating power of SynthAg silver against Beta-Coronavirus, conducted by the Virology and Electron Microscopy Laboratory – Experimental Zooprophylactic Institute of Lombardy and Emilia Romagna.
The active ingredient SynthAg silver was awarded the European Patent for Industrial Invention 2020.
Our company is REGISTERED and VALIDATED as a MEDICAL DEVICE MANUFACTURER with the Ministry of Health.
QUALITY CERTIFICATIONS FOR PRODUCTION PROCESSES
UNI EN ISO 22716 (GMP)
- Despite comprehensive and precise European and national legislation regarding the marketing and use of cosmetic products, until a few years ago, there was no definition of production standards to systematically ensure defined quality levels.
- This “gap” was addressed with the introduction of the international standard EN ISO 22716 in October 2007, establishing the “state of the art” for the industry in the form of Guidelines. Following its adoption by the Italian regulatory body (UNI EN ISO 22716), national companies have increasingly committed to aligning with these Guidelines on Good Manufacturing Practices (GMP) for Cosmetic Products. Certification bodies confirm compliance through assessments of the quality and safety management of products, even at an international level.
Certification of Origin and Quality – 100% Made in Italy
This certification aims to confirm the value of high-quality products of true Italian origin. It is issued by the Institute for the Protection of Italian Manufacturers. The assessment and certification management are carried out by Promindustria S.p.A.
UNI EN ISO 13485 – Medical Devices
The ISO 13485 – Medical Devices standard specifies the requirements for a Quality Management System for regulatory purposes. It is harmonised under the Directive 93/42/EEC and subsequent amendments concerning Medical Devices.
The standard outlines the requirements for a Quality Management System that enables an organisation to demonstrate its ability to provide Medical Devices and related services that comply with customer requirements and regulatory requirements applicable to such devices.
SEAL OF EXCELLENCE
SEAL OF EXCELLENCE
We are proud that our Clusternanotech Group received the “Seal of Excellence” from the European Commission for the MASTERCOW project — a bioinorganic, antibiotic-free therapy for bovine mastitis.
This certificate is the result of a rigorous international evaluation and a recognition of the high scientific and practical value of our innovation
FREE SALE CERTIFICATE
FREE SALE CERTIFICATE
The Free Sale Certificate was issued by the Chamber of Commerce of Emilia for the company CNT SALUS MUNDI SRL. It certifies that the listed veterinary products are freely sold in Italy and the EU and can be exported to Belgium, the Netherlands, Luxembourg, the United Kingdom, the USA, China, Turkey, and India. The official version of the document is the Italian text.
DECLARATION OF QUALITY FOR DAIRY LIVESTOCK
DECLARATION OF QUALITY FOR PAPILLA SEALANT PRODUCT
The Declaration of Quality for Papilla Sealant confirms that the product is a non-medicinal organic sealing paste designed to protect the teats of dairy cows during the dry period. It is not classified as a medical or veterinary medicinal product and does not require registration as such. Manufactured in compliance with European safety and environmental standards, the product undergoes strict quality control and is made from non-toxic ingredients. Efficacy tests confirm its mechanical sealing effect, preventing pathogen entry into the mammary cistern without pharmacological action.
DECLARATION OF QUALITY, SAFETY, AND EFFICACY FOR THE SALVALAT PRODUCT
The declaration of quality, safety, and efficacy for the Salvalat product, developed by CNT LAB S.r.l. It states that the product is neither a medical device nor a phytotherapeutic product and is intended for the internal cleansing of the udders of dairy cows. It confirms compliance with high-quality production standards (ISO 9001:2000 and ISO 13485–2018), the safety of its use, and its effectiveness in reducing biofilm and improving animal health, including the reduction of inflammatory processes.
THE DECLARATION OF NON-CLASSIFICATION FOR THE SALVALAT
The declaration of non-classification for the Salvalat product, developed by CNT LAB S.r.l. It states that the product does not fall into the categories of medicinal, homeopathic, or cosmetic products but is classified as “free trade” due to its mechanical action and the absence of active ingredients. Salvalat is intended for intramammary lavage of dairy cows’ udders to remove biofilm, with confirmed safety and a low level of residues (MRL). Additionally, the document states that in the future, the product may be registered as a phytotherapeutic product by replacing glycolic cucumber extract with Aloe Vera or Cannabidiol (CBD).
DRY-OFF PROTOCOL
SELECTIVE DRY-OFF: SALVALAT ASCIUTTA AND PAPILLA SEAL
The selective dry-off protocol using Salvalat Asciutta and Papilla Seal has been developed to improve the efficiency of the dry period management while minimizing antibiotic use, in line with current guidelines on combating antimicrobial resistance.
DRY-OFF PROTOCOL
The dry-off proposal includes differentiated protocols based on the somatic cell count, using CMT, SALVALAT ASCIUTTA, targeted antibiotics, and the PAPILLA SEAL sealant to ensure a safe drying-off process. For farms not enrolled in ARA, special attention is recommended, while for those with infectious issues, management is entrusted to the farm veterinarian, with the possibility of customised plans.