Established FrameworkIndependent EvaluationPublic Registry

Certification is granted only following documented evidence review, structured assessment, and formal determination of compliance.

Application alone does not constitute approval, provisional status, or endorsement.

The GMT certification pathway is governed by principles of independence, documented verification, procedural consistency, and impartial review.

Fees by Evaluation Phase

Global Medical Trust applies a structured evaluation process. Fees correspond to defined review activities and institutional scope. All fees are quoted in United States Dollars (USD) and are subject to formal scope confirmation following eligibility review.

Phase 1 Application & Eligibility Review

A non-refundable application fee is required prior to formal evaluation.

USD 2,500 – 4,000

This fee covers:

  • • Preliminary eligibility screening
  • • Initial governance and compliance review
  • • Institutional scope determination
  • • Conflict of interest clearance

Payment of the application fee does not guarantee certification approval.

Phase 2 Documentation & Governance Review

Documentation and governance reviews are included within the overall program fee range. This phase examines submitted policies, risk frameworks, and evidence of operational systems.

No separate invoicing is issued at this stage; activities are integrated within the program fee.

Phase 3 Assessment

Assessment activities vary by format and institutional complexity.

Virtual Assessment:
Included within program fee range
On-Site Assessment:
USD 4,000 – 12,000 plus travel and accommodation

On-site assessments may be required for multi-site institutions, high-complexity operations, or expanded scopes.

Phase 4 Determination & Certification Issuance

Certification determination and issuance activities are included within the overall program fee. This phase includes final review of assessment findings and certification decision documentation.

Phase 5 Surveillance & Ongoing Compliance

Surveillance or follow-up compliance activities may be required for certain institutional categories or extended scopes. Fees for ongoing compliance reviews are defined within the certification agreement and may be prorated based on institutional changes.

Standard Fee Ranges (Reference)

For context, typical program fee ranges are:

Direct Clinical Care Institutions (Hospitals & Multi-Site Networks)
USD 18,000 – 42,000
Specialty Clinics & Ambulatory Centers
USD 9,500 – 21,000
Medical Transport & Emergency Services Providers
USD 7,500 – 18,000
International Patient Coordination & Medical Travel Organizations
USD 6,500 – 15,000

Additional Notes

  • • Supplemental evaluation fees may apply for additional campuses, specialty units, or expanded services.
  • • Expedited review services are available upon request and are subject to additional charges.
  • • On-site travel and accommodation expenses are invoiced separately and are the responsibility of the applicant institution.

Billing & Terms

  • • Fees are quoted in USD unless specified otherwise.
  • • Formal quotations are issued following eligibility confirmation and scope definition.
  • • Payment schedules and invoicing terms are defined in the certification agreement.

Global Medical Trust does not operate on a subscription or membership model. Certifications are based on documented compliance and evaluation outcomes.

1. Scope of Evaluation

The certification process evaluates institutional systems rather than individual practitioners. Assessment focuses on:

Governance Structures

Oversight controls and leadership accountability systems

Clinical Safety Systems

Procedural compliance and patient protection protocols

Risk Management

Frameworks for identifying and mitigating institutional risk

Regulatory Alignment

Licensing validation and compliance with applicable standards

Quality Oversight

Continuous quality improvement mechanisms

The scope of review is defined at the time of application and formally documented prior to evaluation.

2. Certification Stages

The GMT certification framework consists of five structured stages.

Stage I

Formal Application and Scope Definition

The applying institution submits required documentation, including:

  • Legal entity identification
  • Licensing and regulatory authorization
  • Organizational governance structure
  • Description of services within certification scope
  • Relevant policy and operational documentation

Acceptance into evaluation does not imply certification.

Stage II

Documented Standards Review

A structured documentation review is conducted to assess conformity with GMT standards. Evaluation may include:

  • Governance records and committee oversight documentation
  • Clinical protocols and infection control systems
  • Risk registers and incident reporting mechanisms
  • Quality assurance policies and performance measurement
  • Credential verification systems and scope-of-practice controls
Stage III

Structured Assessment

Where applicable, GMT conducts a structured verification phase to confirm implementation of documented systems. This may include:

  • Virtual evaluation sessions
  • Committee-based technical review
  • On-site assessment (when required by scope or risk profile)

Assessment is system-focused and evidence-based. Individual clinical outcomes are not independently audited unless required by defined standards.

Stage IV

Compliance Determination Report

Upon completion of evaluation, GMT issues a formal determination report outlining:

  • Areas of conformity
  • Identified non-conformities (if applicable)
  • Required corrective actions
  • Defined remediation timelines

Certification cannot be granted until material non-conformities are resolved and verified.

Stage V

Certification Determination and Registry Entry

Certification is formally granted upon confirmation of compliance. Upon approval:

  • Certification status is issued for a defined validity period (typically two years)
  • The institution is entered into the GMT Public Registry
  • Seal usage authorization is granted under defined policy conditions
  • Certification status is publicly verifiable

3. Ongoing Compliance and Surveillance

Certification is conditional upon continued compliance. Certified institutions are required to:

  • Maintain documented governance and safety systems
  • Notify GMT of material operational or regulatory changes
  • Submit to periodic re-evaluation prior to renewal
  • Cooperate with review in the event of formal complaints or regulatory inquiries

Important: Failure to maintain compliance may result in suspension, review, or revocation of certification status.

4. Impartiality and Independence

GMT certification determinations are governed by the following principles:

Independence

From commercial healthcare providers

Committee-Based Review

Structured multi-stage assessment

Conflict-of-Interest

Disclosure and management controls

Documentation-Based

Decisions based on evidence, not influence

Consistent Application

Uniform standards across all evaluations

Certification decisions are based solely on documented evidence and defined evaluation criteria.

5. Limitations of Certification

GMT certification validates institutional systems and documented operational controls at the time of evaluation.

Certification:

  • Validates institutional systems and controls
  • Reflects documented compliance at time of evaluation
  • Confirms governance and safety frameworks

Does Not:

  • Replace national regulatory authority
  • Guarantee clinical outcomes
  • Constitute endorsement of individual practitioners
  • Serve as legal authorization to practice

Certification reflects structured governance, documented compliance, and operational accountability within the defined scope of evaluation.

Begin Your Certification Journey

Institutions seeking certification are invited to submit a formal application to initiate the process.

Apply for Certification Contact Certification Team

For inquiries regarding the certification process, please contact certification@globalmedicaltrust.org.