New Stetic S.A. is committed to meeting market expectations, ensuring the quality of service, dental anesthetic products, manufactured and/or marketed medical devices, and cosmetics, achieving user safety in the health sector through risk management, continuous improvement, promoting safety in the use of information technology, and effective resource management. We comply with the requirements: ISO 9001, ISO 13485, – CCAA – Storage and conditioning conditions, Regulation (EU) 2017/745 (MDR), Directive 93/42/EEC, 2007/47/EC Annex V and subsequent amendments, – GMP – Good Manufacturing Practices, – GLP – Good Laboratory Practices, – PIC’S – Pharmaceutical Inspection Cooperation Scheme, Resolution RDC No. 658 of March 30, 2022, Brazil, and FDA 21CFR820.

We promote the integral development of our employees and establish controls to protect their health by identifying hazards, evaluating and assessing risks associated with working conditions to establish respective controls leveraged by process improvement, thus protecting our workers, contractors, subcontractors, and visitors.

We manage risks associated with money laundering, terrorist financing, corruption, bribery, and other illicit activities to prevent the use of our organization for such purposes. We also promote ethics, business transparency, and social responsibility as fundamental principles for a good relationship with our stakeholders and strengthen prevention and control elements to avoid labor abuse, discrimination, forced labor, child labor, and other human rights violations.

We are committed to safeguarding the confidentiality, integrity, availability, and privacy of information for employees, customers, suppliers, and the general community through the implementation of data protection policies and information security.

We protect the environment by preventing pollution and making efficient use of the resources used by the organization.

We fulfill our commitment to all stakeholders by applying legal and other acquired requirements.