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Curasept Biosmalto Erosion Protection

Curasept Biosmalto

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WHAT IS
 DENTAL EROSION?

Dental erosion is a chronic, localized pathological process that leads to the progressive loss of the tooth’s hard tissues (enamel and dentine) due to a chemical action not mediated by bacteria.

This loss is caused by reactions between acids of various origins and the tooth surface.

Enamel, already weakened by acids, is further damaged by chewing, daily toothbrushing, and especially by abrasive products or improper oral hygiene techniques, which can worsen tissue loss.

A RISK NOT TO BE UNDERESTIMATED

According to the AIC (Italian Academy of Conservative Dentistry), dental erosion affects 40% of the Italian population and, despite its high prevalence, it is still widely underestimated.²

² Source: AIC (Italian Academy of Conservative Dentistry), 2018.

RISK FACTORS

There are several risk factors that may contribute to dental erosion.
They can be grouped into the following categories:

GERD: Gastroesophageal Reflux Disease

Eating disorders and diets

SPORT:Hyposalivation, exposure to chlorinated water, use of mouthguards

Energy drinks, acidic beverages and alcohol

Pregnancy

Radiotherapy

Asthma medications

Exposure to acids

The Curasept BIOSMALTO EROSION PROTECTION line is enriched with functional ingredients that help protect enamel from acid erosion in the presence of intrinsic risk factors (e.g. gastroesophageal reflux disease, eating disorders) and extrinsic risk factors (e.g. acidic diet).

Curasept Biosmalto Erosion Protection, thanks to its innovative formula, creates a protective film on the enamel, helping to protect it from acidity and regulate oral pH through the presence of the BIO-BALANCE COMPLEX buffering system, composed of Phosphate Buffer and Carnosine.

The Phosphate Buffer helps balance pH fluctuations, while Carnosine provides strong antioxidant properties.

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THE FIRST NON-STAINING CHLORHEXIDINE

The first Curasept mouthwashes and toothpastes with Chlorhexidine featuring A.D.S.® – Anti Discoloration System, an innovative, patented, and clinically tested system that reduces the appearance of yellow-brown spots on the teeth, which is the main side effect of Chlorhexidine.

A.D.S.® inhibits the two chemical reactions leading to pigmentation, without affecting the antiplaque activity of Chlorhexidine. 

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punto elenco blu e azzurro, nei colori inconfondibili del brand Curasept

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Quality Policy

The Quality for CURASEPT S.p.A. is an essential condition to put itself successfully on the market, considering its characteristics and evolution.

The development of the Company and its profit are insured by the continuous search for quality towards excellence through the continuous improvement of its processes and the search for partners with quality systems adapted to our standards.

The Company aims to increase the customer satisfaction through the application of its Quality Management System, including the processes to improve the system and to ensure the compliance with the customer and applicable regulatory requirements.

For this purpose, the Company performs specific risks and opportunities assessment activities, connected to the context, stakeholders and related objectives, in order to identify the areas of system improvements and to define the appropriate actions for the risk control and mitigation and strengthening of its Quality System.

The starting point for the implementation of this policy is the pursuit of the following objectives:

  • Define and implement a Quality Management System according to 9001:2015+A1:2024 e UNI CEI EN ISO 13485:2021 regulation, as Manufacturer of Medical Devices;
  • Define and implement a system of procedures and operating instructions in harmony with the Directive 93/42/CEE, the Regulation (UE) 2017/745 and the Regulation (UE) 2023/607 for the applicable parts and subsequent changes and integrations, which satisfy the essential requirements set out in Annex I;
  • Define and implement a system of procedures in harmony with the Directive 2010/84, the Regulation 1235/2010, the Implementation Regulation n. 520/2012 and in accordance with the objectives of “module I – “Good Vigilance Practices” (GVP).
  • Define and implement, in collaboration with Outsourcers, a quality system and procedures to meet the regulatory requirements for the production of Cosmetics and Food Supplements.
  • Establish and formalize the business organizational structure with the subdivision into areas of competences;
  • Clarify roles and responsibilities of business functions;
  • Define strategies and objectives and assign human and material resources for their achievement;
  • Define accurately business processes and related performance factors;
  • Ensure compliance with qualitative, quantitative and temporal requirements;
  • Constantly monitor the level of adequacy of the system with reference to regulations and laws;
  • Promote initiatives in order to improve the process of motivational and professional growth of human resources, considered as critical resources for future business developments;
  • Ensure the commitment to the satisfaction of requirements and the maintenance of effectiveness of the Quality Management System.

These objectives can be realized thanks to the involvement of the whole Company personnel.

In particular, the Managers of each Function provide their contribution so that the suggested improvements can be proposed to the General Direction, so that the Quality Policy can be a priority element in the choice of business qualitative and organizational strategies.

The involvement of the whole personnel in the improvement of internal and external processes should be aimed at reducing non-compliance and internal and external costs of non-quality; for this reason all employees should feel themselves committed in pursuing this policy.

Training courses, for all business levels, are promoted and planned by the General Direction in order to keep the personnel constantly up to date on the improvements performed for the processes.

The Quality Manual, which is distributed via the SistemaQualità to all process managers and the General Director, should represent a work tool for all Managers and their personnel for the implementation of the Quality Policy.

May 2026

General Direction