Comparison between countries in the subregión de América Central
The information is organized according to the five main categories for implementing EHR systems:
Region: América Central
In this section, all the countries of the subregión de América Central are distributed according to the progress made on their regulatory framework for implementing electronic health records.
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Categories and dimensions for: América Central
This section presents the level of progress of the subregión de América Central in developing the different dimensions of the five categories being analyzed.
Country-by-country breakdown of: Central America
This section provides links to the main legal texts of each country for the different categories and dimensions of their regulatory framework.
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Aspects specific to EHR0
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Patient data protection and secondary use of information50
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Actions of health professionals20
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Role of patients in relation to their health data0
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Standards for health and EHR interoperability0
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- Freedom of information Act
Art #13
- Belize Health Sector Strategic Plan 2014-2024
Objective 5
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Aspects specific to EHR75
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Patient data protection and secondary use of information100
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Actions of health professionals80
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Role of patients in relation to their health data100
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Standards for health and EHR interoperability100
- Law No. 9162
Unified Digital Health Record - Articles 1 and 5
- Regulations of the Unified Digital Health Record
Articles 13 and 14
- Law No. 9162
Unified Digital Health Record - Articles 1 and 5
- Regulations of the Unified Digital Health Record
Articles 13 and 14
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- Law No. 9162
Unified Digital Health Record - Sole Transition Provision
- Law No. 9162
Unified Digital Health Record - Sole Transition Provision, Article 11
- Regulations of the Unified Digital Health Record
Articles 19 and 40
- Law No. 9162
Unified Digital Health Record - Sole Transition Provision, Article 5
- Law No. 9162
Unified Digital Health Record - Sole Transition Provision, Article 6
- Law No. 8968
Protection of Individuals Regarding the Processing of Their Personal Data Act, Article 10
- Law No. 8968
Protection of Individuals Regarding the Processing of Their Personal Data Act, Articles 8 and 9
- Law No. 8454
Certificates, Digital Signatures, and Electronic Documents Act, Articles 8, 9, and 10
- Law No. 8454
Certificates, Digital Signatures, and Electronic Documents Act, Articles 3, 4, 5, 6, and 7
- Regulations of the Unified Digital Health Record
Articles 12 and 19
- Law No. 8968
Protection of Individuals Regarding the Processing of Their Personal Data Act, Article 9
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- Law No. 9162
Unified Digital Health Record - Article 5
- Decree No. 39984-S
Regulations for the use and operation of the automated digital prescription system for psychotropic and narcotic drugs
- Session No. 7366 of September 1999
Costa Rican Social Security Fund Health Record Regulations - Article 40
- Law No. 8968
Protection of Individuals Regarding the Processing of Their Personal Data Act, Article 5
- Law No. 9162
Unified Digital Health Record - Article 5
- Law No. 8968
Protection of Individuals Regarding the Processing of Their Personal Data Act, Article 7
- Law No. 8968
Protection of Individuals Regarding the Processing of Their Personal Data Act, Article 7
- Ley 8239
Derechos y deberes de las personas usuarias de los servicios de salud públicos y privados Art# 2
- No. 39652-S-MICIT
Regulations on the use of health data standards in patient care and creation of the National Health Data Standardization Committee
- No. 39652-S-MICIT
Regulations on the use of health data standards in patient care and creation of the National Health Data Standardization Committee
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Aspects specific to EHR100
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Patient data protection and secondary use of information100
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Actions of health professionals60
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Role of patients in relation to their health data100
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Standards for health and EHR interoperability0
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records
- Resolution No. 941
Chapter VI - Transition, final, and repealing provisions - Transition Provision - Article 87 Public and private institutions that do not meet the security requirements established in Chapters III and IV of this regulation shall prepare a plan for compliance with these provisions within a period of no less than five years
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records, Article 1
- Decree No. 307
Duties and Rights of Patients and Health Care Providers Act, Article 33
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records, Article 75
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records, Article 12
- Decree No. 133
Electronic Signature Act, Article 14
- Decree No. 307
Duties and Rights of Patients and Health Care Providers Act, Article 16
- Decree No. 133
Electronic Signature Act, Article 14
- Decree No. 133
Electronic Signature Act, Article 14
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records - Article 23
- Decree No. 307
Duties and Rights of Patients and Health Care Providers Act, Article 33
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- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records - Article 11
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records - Article 13
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records - Article 7
- Resolution No. 941
Technical regulation on the composition, custody, and querying of medical records - Articles 6 and 60
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Aspects specific to EHR0
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Patient data protection and secondary use of information50
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Actions of health professionals40
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Role of patients in relation to their health data75
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Standards for health and EHR interoperability0
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- Decree No. 57-2008
Access to Public Information Act, Articles 30 and 32
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- Decree No. 57-2008
Access to Public Information Act, Article 32
- Decree No. 47-2008
Recognition of Electronic Communications and Signatures Act, Article 1
- Government Resolution No. 262-2009
Government Resolution No. 262-2009 Amendments to the regulations of the Recognition of Electronic Communications and Signatures Act, Article 1
- Government Resolution No. 135-2009
Amendments to the regulations of the Recognition of Electronic Communications and Signatures Act, Article 1
- Decree No. 47-2008
Does not refer to health. Decree No. 47-2008 Recognition of Electronic Communications and Signatures Act, Article 1. The legal and technical certainty of electronic contracts, communications, and signatures must be ensured by establishing their functional equivalence to paper-based documents and handwritten signatures.
- Government Resolution No. 135-2009
Regulations of the Recognition of Electronic Communications and Signatures Act Government Resolution
- Resolution No. 262-2009
Amendments to the regulations of the Recognition of Electronic Communications and Signatures Act
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- Decree No. 57-2008
Access to Public Information Act, Article 31
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- Decree No. 57-2008
Access to Public Information Act, Article 34
- Decree No. 57-2008
Access to Public Information Act, Articles 16 and 41
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Aspects specific to EHR0
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Patient data protection and secondary use of information50
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Actions of health professionals40
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Role of patients in relation to their health data75
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Standards for health and EHR interoperability0
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- Decree No. 170-2006
Transparency and Access to Public Information Act and its regulations
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- Regulation No. 65-91
Health Code - Articles 179, 180, 181, and 182
- Decree No. 149-2013
Electronic Signatures Act, Article 2
- Decree No. 33-2020
No. 35217 of April 3, 2020: Relief for the Productive Sector and Workers from the Effects of the COVID-19 Pandemic Act - Article 38
- Decree No. 149-2013
Electronic Signatures Act, Article 8
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- Decree No. 170-2006
Transparency and Access to Public Information Act and its regulations - Article 42
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- Decree No. 170-2006
Transparency and Access to Public Information Act and its regulations - Article 46
- Decree No. 170-2006
Transparency and Access to Public Information Act and its regulations - Articles 3 and 49
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Aspects specific to EHR75
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Patient data protection and secondary use of information100
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Actions of health professionals100
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Role of patients in relation to their health data100
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Standards for health and EHR interoperability100
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Article 10
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information appendix B
- NOM-024-SSA3-2012
Electronic record information systems for health. Health Information Exchange
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information appendix B
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- Law No. DOF 05-07-2010
Federal Law on Protection of Personal Data Held by Private-Sector Parties.
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Article 10
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Article 5
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Article 10 - Regulatory appendix 3.3.7
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Articles 3.14 and 5.1.15
- Law No. DOF 11-01-2012
Electronic signatures
- Law No. DOF 11-01-2012
Electronic signatures - Article 7
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Article 5.1.15
- Law No. DOF 05-07-2010
Federal Law on Protection of Personal Data Held by Individuals, Article 10
- NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Regulatory appendix A: 1.2.1
- DOF 11-01-2012
Decree issuing the Advanced Electronic Signature Law. Article 8
- Official Mexican Standard NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information - Article 5
- DOF 11-01-2012
Decree issuing the Advanced Electronic Signature Law. Article 22
- DOF 11-01-2012
Decree issuing the Advanced Electronic Signature Law. Article 22
- Official Mexican Standard NOM-024-SSA3-2010
Establishes the functional objectives and functionalities that products of the Electronic Health Record Systems should have in order to ensure the interoperability, processing, interpretation, confidentiality, and security of information in electronic health records, as well as the use of standards and catalogs for that information. Another reason why regulating the use of Electronic Health Records is essential is that doing so will make health information available when making decisions during everything from patient care to public health policy development. This will be made possible by establishing national standards and catalogs that ensure the interoperability of existing applications at the various public, private, and social institutions that provide health services to the public.
- Official Mexican Standard NOM-024-SSA3-2010, Section 3.14 Codes:
Referring to a vocabulary, set of codes, databases, terminologies, or catalogs. 3.17 Classification of procedures in medicine: Mandatory standard in Mexico for coding and generating statistics for both surgical and non-surgical (diagnostic and therapeutic) medical procedures for national comparability purposes. This standard uses the version currently in force in Mexico 3.18 International Statistical Classification of Diseases and Related Health Problems: International standard that is mandatory in Mexico for coding and generating uniform morbidity and mortality statistics for national and international comparability purposes. This standard uses the version currently in force in Mexico. 3.19 International Classification of Functioning, Disability, and Health : International standard that is mandatory in Mexico for studying, coding, and generating functioning and disability statistics for national and international comparability purposes. This standard uses the version currently in force in Mexico
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Aspects specific to EHR0
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Patient data protection and secondary use of information100
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Actions of health professionals60
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Role of patients in relation to their health data75
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Standards for health and EHR interoperability0
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- Regulations of Law No. 787
Personal Data Protection Act, Article 3
- Law No. 423
Health Act, Article 5
- Regulations of Law No. 787
Personal Data Protection Act, Article 13
- Regulations of Law No. 787
Personal Data Protection Act, Article 11
- Regulations of Law No. 787
Personal Data Protection Act, Article 7
- Law No. 729
Electronic Signature
- Law No. 729
Electronic Signature
- Law No. 423
Health Act
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- Regulations of Law No. 787
Personal Data Protection Act, Article 8
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- Regulations of Law No. 787
Personal Data Protection Act, Article 17
- Regulations of Law No. 787
Personal Data Protection Act, Article 7
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Aspects specific to EHR25
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Patient data protection and secondary use of information75
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Actions of health professionals40
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Role of patients in relation to their health data75
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Standards for health and EHR interoperability50
- Resolution No. 0697
Por medio de la cual se adopta el convenio para el sistema electrónico de información de salud (SEIS)
- Resolution No. 945
Approves the organizational structure of the teams responsible for implementing the Electronic Health Information System (SEIS) and of the electronic clinical records. It also includes a procedure manual for SEIS users and an SEIS implementation agreement.
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- Law No. 81
Personal data protection
- Law No. 43
Defines and regulates electronic documents and signatures and certification entities in e-commerce and the exchange of electronic documents
- Law No. 68
Regulates the rights and obligations of patients regarding information and free and informed decision-making— Article 48
- Law No. 68
Regulates the rights and obligations of patients regarding information and free and informed decision-making—Article 45
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- Law No. 68
Regulates the rights and obligations of patients regarding information and free and informed decision-making— Article 48
- Law No. 68
Regulates the rights and obligations of patients regarding information and free and informed decision-making— Article 67
- Law No. 97-2019
Amends and adds articles to Law No. 1 of 2001 on medicines and other human health products, Article 16
- Executive Decree No. 1458
Establishes the implementing regulations for Law No. 68 of November 20, 2003, which regulates the rights and obligations of patients regarding information and free and informed decision-making—Chapter III
- Executive Decree No. 1458
Establishes the implementing regulations for Law No. 68 of November 20, 2003, which regulates the rights and obligations of patients regarding information and free and informed decision-making—Article 47
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- Executive Decree No. 1458
Establishes the implementing regulations for Law No. 68 of November 20, 2003, which regulates the rights and obligations of patients regarding information and free and informed decision-making—Article 7
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