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Certification technologies: Agility in signing documents and serving patients; Practicality and reduction in the use of paper — which generates savings; The electronic signature has probative force; Possibility of subscribing from anywhere and on any device; The digital certificate has the same validity as the CPF and CNPJ; Greater security for the authenticity of the signatory and the integrity of the signed medical document. Standards for electronic signatures in healthcare Digital certificates and digital signatures were already accepted and used in some contexts, but new regulations are expanding the possibilities and driving digital transformation in the healthcare sector. Find out more below about the rules for using electronic signatures in the healthcare sector. Supplemental Health Information Exchange (TISS) The TISS standard , implemented by the National Supplementary Health Agency (ANS), was established as a mandatory model for electronic data exchanges between health plan operators and service providers in an area.
The main objective of TISS is to standardize the authorization processes for exams and procedures in hospitals, service charges and proof of presence. In other words, the standard monitors the economic, financial and assistance of health plan operators and forms part of the Electronic Health Record. Its main advantages are: Improving communication between actors in the healt Singapore Phone Numbers Million List h sector; Reduction of administrative costs; Facilitation in obtaining information for epidemiological studies; Improvements in the quality of assistance to the beneficiary. SBIS/CFM Since , the Brazilian Society of Health Informatics (SBIS) and the Federal Council of Medicine (CFM) have worked together to standardize the use of digital certification in the health sector in information exchange systems.

A certification process for Electronic Health Record Systems (S-RES) was then developed , a system that captures, stores, presents, transmits or prints identified health information, that is, information that allows individualizing a patient through their name and identification number, such as CPF. The process evaluates and certifies quality aspects of S-RES, such as functionalities, structure, information security and adherence to legislation. Its objectives are the following: Increase the information security of electronic records; Evaluate the software ’s adherence to regulations and standards for legal support for eliminating paper; Encourage technological evolution; Improve the quality of S-RES; Optimize patient safety and the quality of healthcare. The most recent manuals, published in March , include teleconsultation, teleinterconsultation, teletriage and digital prescription modalities.
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