---
schema_version: "1"
id: dfebffaa08dbabf3d519b56d3b8e6473c9be2a32f922a1841ea55bfa10cd8a8d
title: ResearchStudyProtocolInfo
collection: legacydeveloper
version: current
locale: en-us
portal_url: https://docs.salesforce.com/legacydeveloper/current/en-us/life_sciences_dev_guide/sforce_api_objects_researchstudyprotocolinfo.md
canonical_url: https://developer.salesforce.com/docs/atlas.en-us.life_sciences_dev_guide.meta/life_sciences_dev_guide/sforce_api_objects_researchstudyprotocolinfo.htm
source_site: developer.salesforce.com
content_type: documentation
content_hash: 9f1870863628bf39fd1c395764a1b5a2dec1042d7e56a3a8f281cf67fa690c9d
description: Represents details of the research study protocol document. This object is available in API version 62.0 and later.
---
# ResearchStudyProtocolInfo

Represents details of the research study protocol document. This object is available in API version 62.0 and later.

## Supported Calls

create(), delete(), describeLayout(), describeSObjects(), getDeleted(), getUpdated(), query(), retrieve(), search(), undelete(), update(), upsert()

## Fields

### Content

- **Type**: textarea
- **Properties**: Create, Update
- **Description**: The content text for the research study protocol.

### ContentType

- **Type**: picklist
- **Properties**: Create, Filter, Group, Restricted picklist, Sort, Update
- **Description**: Specifies the type of the content stored.
- **Possible values**:
    - Abbreviations
    - Adverse Events Classification
    - Adverse Events Definition
    - Adverse Events Participant Reporting
    - Adverse Events Reporting
    - Analysis Dataset Criteria
    - Analysis Population Criteria
    - Background
    - Biospecimen Sample Retention
    - Clinical Masking Description
    - Clinical Monitoring
    - Confidentiality and Privacy
    - Conflict of Interest Policy
    - Data Handling and Record Keeping
    - Dosage Justification
    - End of Study Procedure
    - Event Assessment Frequency and Time Period
    - Gender Eligibility Description
    - Informed Consent Process
    - Intervention Benefits
    - Intervention Compliance
    - Intervention Discontinuation
    - Intervention Dosing and Administration
    - Intervention Preparation
    - Intervention Risks
    - Intervention Risks and Benefits Assessments
    - Intervention Storage and Stability
    - Lost to Follow-up
    - Pregnancy Reporting
    - Primary Endpoint Analysis
    - Protocol Deviations
    - Publication and Data Sharing Policy
    - Quality Assurance and Control
    - Safety Analysis
    - Safety Oversight
    - Sample Size Determination
    - Secondary Endpoint Analysis
    - Serious Adverse Events Definition
    - Serious Adverse Events Reporting
    - Special Interest Reporting
    - Statistical Analysis Summary
    - Study Design
    - Study Discontinuation and Closure
    - Study Population
    - Study Population Description
    - Study Record Retention Period
    - Study Scientific Rationale
    - Subgroup Analysis
    - Summary

### LastReferencedDate

- **Type**: dateTime
- **Properties**: Filter, Nillable, Sort
- **Description**: The timestamp for when the current user last referenced a record related to this record.

### LastViewedDate

- **Type**: dateTime
- **Properties**: Filter, Nillable, Sort
- **Description**: The timestamp for when the current user last viewed this record. If this value is null, it’s possible that this record was referenced (LastReferencedDate) and not viewed.

### Name

- **Type**: string
- **Properties**: Autonumber, Defaulted on create, Filter, idLookup, Sort
- **Description**: The name of the research study protocol information.

### ResearchStudyId

- **Type**: reference
- **Properties**: Create, Filter, Group, Sort
- **Description**: The research study associated with the content.
    
    This field is a relationship field.
- **Relationship Name**: ResearchStudy
- **Relationship Type**: Master-detail
- **Refers To**: ResearchStudy (the master object)