Data elements for the DDCC Core Data Set for Vaccination Status.

A vaccination event.

Generic description of the vaccine or vaccine sub-type. e.g. COVID-19 mRNA vaccine, HPV vaccine.

The brand or trade name used to refer to the vaccine received.

Name of the manufacturer of the vaccine received. e.g. Serum institute of India, AstraZeneca. If vaccine manufacturer is unknown, market authorization holder is REQUIRED.

Name of the market authorization holder of the vaccine received. If market authorization holder is unknown, vaccine manufacturer is REQUIRED.

Lot number or batch number of vaccination.

Date in which the vaccine was provided.

Date upon which provided vaccination is considered valid.

Vaccine dose number.

Total expected doses as defined by Member State care plan and immunization programme policies.

The country in which the individual has been vaccinated.

The name or identifier of the vaccination facility responsible for providing the vaccination.

REQUIRED for PAPER vaccination certificates ONLY. The health worker who provided the vaccination or the supervising clinician's hand-written signature.

OPTIONAL for DIGITAL and PAPER vaccination certificates. The unique identifier for the health worker as determined by the member state. There can be more than one unique identifier used. (e.g. system generated ID, health profession number, cryptographic signature, or any other form of health worker unique identifier). This can be used in lieu of a paper-based signature.

Name of disease vaccinated against (such as COVID-19).

Date on which the next vaccination should be administered, if a next dose is REQUIRED.

Data elements for the DDCC Core Data Set for Vaccination Status.

The full name of the person.

The person's date of birth (DOB) if known. If unknown, use given DOB for administrative purposes

Unique identifier for the person, according to the policies applicable to each country. There can be more than one unique identifier used to link records. (e.g. national ID, health ID, immunization information system ID, medical record ID).

Metadata associated with the certificate

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Certificate issuer.

Key ID

Health certificate identifier (HCID).

DDCC Identifier

Certificate schema version

Certificate validity period.

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Start date of certificate validity.

If the low element is missing, the meaning is that the low boundary is not known.

End date of certificate validity.

The high value includes any matching date/time. i.e. 2012-02-03T10:00:00 is in a period that has an end value of 2012-02-03.

A vaccination event.

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Generic description of the vaccine or vaccine sub-type. e.g. COVID-19 mRNA vaccine, HPV vaccine.

The brand or trade name used to refer to the vaccine received.

Name of the manufacturer of the vaccine received. e.g. Serum institute of India, AstraZeneca. If vaccine manufacturer is unknown, market authorization holder is REQUIRED.

Name of the market authorization holder of the vaccine received. If market authorization holder is unknown, vaccine manufacturer is REQUIRED.

Lot number or batch number of vaccination.

Date in which the vaccine was provided.

Date upon which provided vaccination is considered valid.

Vaccine dose number.

Total expected doses as defined by Member State care plan and immunization programme policies.

The country in which the individual has been vaccinated.

The name or identifier of the vaccination facility responsible for providing the vaccination.

REQUIRED for PAPER vaccination certificates ONLY. The health worker who provided the vaccination or the supervising clinician's hand-written signature.

OPTIONAL for DIGITAL and PAPER vaccination certificates. The unique identifier for the health worker as determined by the member state. There can be more than one unique identifier used. (e.g. system generated ID, health profession number, cryptographic signature, or any other form of health worker unique identifier). This can be used in lieu of a paper-based signature.

Name of disease vaccinated against (such as COVID-19).

Date on which the next vaccination should be administered, if a next dose is REQUIRED.

Data elements for the DDCC Core Data Set for Vaccination Status.

The full name of the person.

The person's date of birth (DOB) if known. If unknown, use given DOB for administrative purposes

Unique identifier for the person, according to the policies applicable to each country. There can be more than one unique identifier used to link records. (e.g. national ID, health ID, immunization information system ID, medical record ID).

Metadata associated with the certificate

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Certificate issuer.

Key ID

Health certificate identifier (HCID).

DDCC Identifier

Certificate schema version

Certificate validity period.

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Start date of certificate validity.

If the low element is missing, the meaning is that the low boundary is not known.

End date of certificate validity.

The high value includes any matching date/time. i.e. 2012-02-03T10:00:00 is in a period that has an end value of 2012-02-03.

A vaccination event.

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Generic description of the vaccine or vaccine sub-type. e.g. COVID-19 mRNA vaccine, HPV vaccine.

The brand or trade name used to refer to the vaccine received.

Name of the manufacturer of the vaccine received. e.g. Serum institute of India, AstraZeneca. If vaccine manufacturer is unknown, market authorization holder is REQUIRED.

Name of the market authorization holder of the vaccine received. If market authorization holder is unknown, vaccine manufacturer is REQUIRED.

Lot number or batch number of vaccination.

Date in which the vaccine was provided.

Date upon which provided vaccination is considered valid.

Vaccine dose number.

Total expected doses as defined by Member State care plan and immunization programme policies.

The country in which the individual has been vaccinated.

The name or identifier of the vaccination facility responsible for providing the vaccination.

REQUIRED for PAPER vaccination certificates ONLY. The health worker who provided the vaccination or the supervising clinician's hand-written signature.

OPTIONAL for DIGITAL and PAPER vaccination certificates. The unique identifier for the health worker as determined by the member state. There can be more than one unique identifier used. (e.g. system generated ID, health profession number, cryptographic signature, or any other form of health worker unique identifier). This can be used in lieu of a paper-based signature.

Name of disease vaccinated against (such as COVID-19).

Date on which the next vaccination should be administered, if a next dose is REQUIRED.