---
title: "FedRAMP, FedRAMP | MedTech Terms"
description: "U.S. government-wide program that standardizes security assessment, authorization, and continuous monitoring for cloud services sold to federal agencies."
lang: en
json-ld: |
  {
    "@context": "https://schema.org",
    "@graph": [
      {
        "@type": "DefinedTerm",
        "@id": "https://medtechterms.com/terms/fedramp#term",
        "name": "FedRAMP",
        "alternateName": [
          "FedRAMP",
          "Federal Risk and Authorization Management Program"
        ],
        "description": "FedRAMP (Federal Risk and Authorization Management Program) is the U.S. federal government's standardized approach for assessing and authorizing cloud services. Cloud Service Providers (CSPs) work with a Third Party Assessment Organization (3PAO) to evaluate a defined set of NIST SP 800-53 controls (tailored to the FedRAMP Low, Moderate, or High baseline) and receive an Authorization to Operate (ATO) from either an individual agency or the Joint Authorization Board. Once authorized, a CSP's package can be reused by other agencies, a 'do once, use many times' model.",
        "url": "https://medtechterms.com/terms/fedramp",
        "termCode": "fedramp",
        "inDefinedTermSet": {
          "@type": "DefinedTermSet",
          "name": "MedTech Terms",
          "url": "https://medtechterms.com/terms"
        }
      },
      {
        "@type": "Article",
        "@id": "https://medtechterms.com/terms/fedramp#article",
        "headline": "FedRAMP, FedRAMP",
        "description": "U.S. government-wide program that standardizes security assessment, authorization, and continuous monitoring for cloud services sold to federal agencies.",
        "url": "https://medtechterms.com/terms/fedramp",
        "mainEntityOfPage": {
          "@type": "WebPage",
          "@id": "https://medtechterms.com/terms/fedramp"
        },
        "about": {
          "@id": "https://medtechterms.com/terms/fedramp#term"
        },
        "articleSection": "Cybersecurity",
        "inLanguage": "en",
        "keywords": "FedRAMP, FedRAMP, Federal Risk and Authorization Management Program, Cybersecurity, medical device, MedTech",
        "author": {
          "@type": "Person",
          "name": "Christian Espinosa",
          "jobTitle": "Founder, Blue Goat Cyber",
          "url": "https://bluegoatcyber.com"
        },
        "publisher": {
          "@type": "Organization",
          "name": "MedTech Terms",
          "url": "https://medtechterms.com"
        },
        "isPartOf": {
          "@type": "WebSite",
          "name": "MedTech Terms",
          "url": "https://medtechterms.com"
        },
        "datePublished": "2026-06-20",
        "dateModified": "2026-06-20",
        "citation": [
          {
            "@type": "CreativeWork",
            "name": "FedRAMP",
            "url": "https://www.fedramp.gov/",
            "publisher": {
              "@type": "Organization",
              "name": "GSA"
            }
          },
          {
            "@type": "CreativeWork",
            "name": "FedRAMP Marketplace",
            "url": "https://marketplace.fedramp.gov/",
            "publisher": {
              "@type": "Organization",
              "name": "GSA"
            }
          },
          {
            "@type": "CreativeWork",
            "name": "CISA - Healthcare and Public Health Sector",
            "url": "https://www.cisa.gov/topics/critical-infrastructure-security-and-resilience/critical-infrastructure-sectors/healthcare-and-public-health-sector",
            "publisher": {
              "@type": "Organization",
              "name": "CISA"
            }
          }
        ],
        "mentions": [
          {
            "@type": "DefinedTerm",
            "@id": "https://medtechterms.com/terms/soc-2#term",
            "name": "SOC 2",
            "url": "https://medtechterms.com/terms/soc-2"
          },
          {
            "@type": "DefinedTerm",
            "@id": "https://medtechterms.com/terms/hitrust#term",
            "name": "HITRUST CSF",
            "alternateName": "HITRUST",
            "url": "https://medtechterms.com/terms/hitrust"
          },
          {
            "@type": "DefinedTerm",
            "@id": "https://medtechterms.com/terms/nist-800-53#term",
            "name": "NIST SP 800-53 / 800-171",
            "alternateName": "NIST 800-53/171",
            "url": "https://medtechterms.com/terms/nist-800-53"
          },
          {
            "@type": "DefinedTerm",
            "@id": "https://medtechterms.com/terms/iso-27001#term",
            "name": "ISO/IEC 27001",
            "alternateName": "ISO 27001",
            "url": "https://medtechterms.com/terms/iso-27001"
          },
          {
            "@type": "DefinedTerm",
            "@id": "https://medtechterms.com/terms/hipaa#term",
            "name": "HIPAA",
            "alternateName": "HIPAA",
            "url": "https://medtechterms.com/terms/hipaa"
          },
          {
            "@type": "DefinedTerm",
            "@id": "https://medtechterms.com/terms/samd#term",
            "name": "Software as a Medical Device",
            "alternateName": "SaMD",
            "url": "https://medtechterms.com/terms/samd"
          }
        ]
      },
      {
        "@type": "BreadcrumbList",
        "itemListElement": [
          {
            "@type": "ListItem",
            "position": 1,
            "name": "Home",
            "item": "https://medtechterms.com/"
          },
          {
            "@type": "ListItem",
            "position": 2,
            "name": "Terms",
            "item": "https://medtechterms.com/terms"
          },
          {
            "@type": "ListItem",
            "position": 3,
            "name": "Cybersecurity",
            "item": "https://medtechterms.com/terms?cat=Cybersecurity"
          },
          {
            "@type": "ListItem",
            "position": 4,
            "name": "FedRAMP",
            "item": "https://medtechterms.com/terms/fedramp"
          }
        ]
      }
    ]
  }
---

[

MedTech Terms

The authoritative reference



](/)

Browse

Learn

[Latest](/latest)

About

1.  [Home](/)
2.  /
3.  [Terms](/terms)
4.  /
5.  [Cybersecurity](/terms?cat=Cybersecurity)
6.  /
7.  FedRAMP

[All terms](/terms)

Cybersecurity [Connected & Cyber-Physical Devices](/ecosystems/connected-devices)FedRAMP 

# FedRAMP

U.S. government-wide program that standardizes security assessment, authorization, and continuous monitoring for cloud services sold to federal agencies.

Reviewed by [Christian Espinosa, Founder, Blue Goat Cyber](/authors/christian-espinosa) Last reviewed June 20, 2026 

## Definition

FedRAMP (Federal Risk and Authorization Management Program) is the U.S. federal government's standardized approach for assessing and authorizing cloud services. Cloud Service Providers (CSPs) work with a Third Party Assessment Organization (3PAO) to evaluate a defined set of NIST SP 800-53 controls (tailored to the FedRAMP Low, Moderate, or High baseline) and receive an Authorization to Operate (ATO) from either an individual agency or the Joint Authorization Board. Once authorized, a CSP's package can be reused by other agencies, a 'do once, use many times' model. 

What the regulation says

Required by OMB policy for federal agency use of cloud services. Aligned with FISMA. FedRAMP control baselines are derived from NIST SP 800-53; the program is jointly operated by GSA, DoD, DHS, and OMB. 

## What this means in practice

For MedTech, FedRAMP becomes relevant when selling cloud-hosted  [SaMD](/terms/samd), AI/ML platforms,  [RPM](/terms/remote-patient-monitoring) services, or clinical trial software to the VA, IHS, DoD/MHS (Military Health System), or any HHS agency. The VA and DoD increasingly require FedRAMP Moderate as a baseline for any cloud service handling veteran or service member health data. Even private-sector hospitals are starting to reference FedRAMP Moderate as a credibility marker for cloud-hosted device backends. 

Common pitfalls

-   • Sponsoring an ATO with a single agency when you actually need a Joint Authorization Board (JAB) Provisional ATO for broad federal reuse. 
-   • Assuming FedRAMP Low is sufficient for health data, VA and MHS deployments typically require Moderate or High. 
-   • Underestimating continuous monitoring, monthly POA&Ms, annual assessments, and significant-change reauthorization are non-negotiable. 

## Related terms

Grouped by theme 

### Editor's picks

· Hand-selected related concepts 

[

Cybersecurity

HIPAA(HIPAA) 

U.S. federal law governing the privacy and security of protected health information.





](/terms/hipaa)[

Cybersecurity

HITRUST CSF(HITRUST) 

Healthcare-focused certifiable security framework that consolidates HIPAA, NIST, ISO 27001, and other authorities into a unified control set.





](/terms/hitrust)[

Cybersecurity

ISO/IEC 27001(ISO 27001) 

International standard for information security management systems (ISMS), often required of MedTech vendors by enterprise customers.





](/terms/iso-27001)[

Cybersecurity

NIST SP 800-53 / 800-171(NIST 800-53/171) 

Federal control catalogs (800-53) and CUI-handling requirements (800-171) often referenced in MedTech contracts.





](/terms/nist-800-53)

### More in Cybersecurity

· Same category 

[

Cybersecurity

SOC 2

AICPA attestation report on a service organization's controls over Security, Availability, Processing Integrity, Confidentiality, and Privacy, the standard SaaS trust artifact.





](/terms/soc-2)[

Cybersecurity

AAMI SW96

AAMI/ANSI standard establishing requirements for medical-device cybersecurity activities throughout the lifecycle.





](/terms/aami-sw96)[

Cybersecurity

AAMI TIR57

AAMI Technical Information Report providing MedTech-specific guidance on cybersecurity risk management.





](/terms/aami-tir57)[

Cybersecurity

AAMI TIR97(TIR97) 

AAMI Technical Information Report on post-market security risk management for medical device manufacturers, the operational companion to TIR57.





](/terms/aami-tir97)

Cited by

Where this term appears across MedTech Terms.

Ecosystems (1)

-   [Connected & Cyber-Physical Devices](/ecosystems/connected-devices)

## Primary references

3 sources 

Link health:  3 verified · last checked 2026-06-20 

GSA· 2 CISA· 1 

1.  [1 
    
    FedRAMP
    
    Verified 
    
    GSA · fedramp.gov 
    
    
    
    ](https://www.fedramp.gov/)
2.  [2 
    
    FedRAMP Marketplace
    
    Verified 
    
    GSA · marketplace.fedramp.gov 
    
    
    
    ](https://marketplace.fedramp.gov/)
3.  [3 
    
    CISA - Healthcare and Public Health Sector
    
    Verified 
    
    CISA · cisa.gov 
    
    
    
    ](https://www.cisa.gov/topics/critical-infrastructure-security-and-resilience/critical-infrastructure-sectors/healthcare-and-public-health-sector)

Inline markers like \[1\]  jump to the matching reference above.

Sponsor note

### Working on medical device cybersecurity?

Blue Goat Cyber specializes in MedTech cybersecurity - threat modeling, SBOMs, penetration testing, and FDA premarket submissions.

[Book a 30-minute discovery session](https://go.bluegoatcyber.com/meetings/blue-goat-cyber/discovery-session)

-   No obligation
-   Expert-led from minute one
-   NDA available on request

MedTech Terms is a community resource sponsored by [Blue Goat Cyber](https://bluegoatcyber.com). Definitions are independent of any vendor.

On this term

Category

Cybersecurity

Acronym

FedRAMP

Sources

3

Updated

6/20/2026

[Compare with another term](/compare?a=fedramp)

Learn in 60 seconds

Card Lesson Quiz

U.S. government-wide program that standardizes security assessment, authorization, and continuous monitoring for cloud services sold to federal agencies.

-   · For MedTech, FedRAMP becomes relevant when selling cloud-hosted SaMD, AI/ML platforms, RPM services, or clinical trial software to the VA, IHS, DoD/MHS (Military Health System), or any HHS agency. 
-   · The VA and DoD increasingly require FedRAMP Moderate as a baseline for any cloud service handling veteran or service member health data. 
-   · Even private-sector hospitals are starting to reference FedRAMP Moderate as a credibility marker for cloud-hosted device backends. 

Remember this

Watch out: Sponsoring an ATO with a single agency when you actually need a Joint Authorization Board (JAB) Provisional ATO for broad federal reuse.

Related terms

-   [SOC 2 ](/terms/soc-2)
-   [HITRUST CSF(HITRUST) ](/terms/hitrust)
-   [NIST SP 800-53 / 800-171(NIST 800-53/171) ](/terms/nist-800-53)
-   [ISO/IEC 27001(ISO 27001) ](/terms/iso-27001)
-   [HIPAA(HIPAA) ](/terms/hipaa)
-   [Software as a Medical Device(SaMD) ](/terms/samd)

You may also need

Auto-suggested from Cybersecurity and shared keywords.

-   [AAMI TIR97(TIR97) ](/terms/aami-tir97)
-   [Premarket Cybersecurity Submission ](/terms/premarket-cybersecurity)
-   [Penetration Testing ](/terms/pen-test)
-   [Threat Modeling ](/terms/threat-modeling)
-   [Section 524B of the FD&C Act(524B) ](/terms/section-524b)
-   [CISA Known Exploited Vulnerabilities Catalog(KEV) ](/terms/kev)

[All Cybersecurity terms](/terms?cat=Cybersecurity)

From the Blue Goat network

Related resources and services on this topic.

-   [
    
    MedTech Cybersecurity Standards 
    
    Authoritative reference for the standards and guidances behind medical device cybersecurity.
    
    ](https://medtechcyberstandards.com)
-   [
    
    MedTech Cyber Tips 
    
    Practical, organized tips for medical device cybersecurity teams.
    
    ](https://medtechcybertips.com)
-   [
    
    MedTech Cybersecurity Crosswalk 
    
    International crosswalk of medical device cybersecurity requirements across regulators.
    
    ](https://mdccrosswalk.com)
-   [
    
    Code Blue 
    
    Real medical device cybersecurity incidents and their lessons.
    
    ](https://codebluechart.com)

MedTech Terms 

An authoritative, plain-language reference for the regulatory, quality, cybersecurity, and software terms that shape modern medical devices.

Browse

-   [All terms](/terms)
-   [A–Z index](/a-z)
-   [Categories](/categories)
-   [Ecosystems](/ecosystems)
-   [Learning paths](/paths)
-   [Compare terms](/compare)
-   [Quiz](/quiz)

Resources

-   [FDA Medical Devices](https://www.fda.gov/medical-devices)
-   [EU MDR](https://eur-lex.europa.eu/eli/reg/2017/745/oj)
-   [IMDRF](https://www.imdrf.org/)
-   [Methodology](/methodology)
-   [Changelog](/changelog)
-   [Editor: Christian Espinosa](/authors/christian-espinosa)
-   [About this site](/about)

© 2026 MedTech Terms. Reference content for educational purposes - not regulatory advice. A community resource sponsored by [Blue Goat Cyber](https://bluegoatcyber.com)