INSAN Trials

Clinical Trials in Oman

From feasibility to full-service CRO support—local expertise, site network, and regulatory navigation.

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ICH-GCP Aligned

International standards compliance

QMS Certified

Audit-ready processes

48-Hour SLA

Guaranteed response time

Regulatory Expertise

Oman MoH navigation

CRO Starter Packages

Feasibility Assessment

2-4 weeks

Site evaluation, patient population analysis, and regulatory landscape assessment.

Start-Up Support

4-8 weeks

IRB/Ethics submission, site contracts, and essential document preparation.

Registry-in-a-Box

Ongoing

Real-world evidence registry design and execution for observational studies.

Site Readiness Program

8-12 weeks

Capability assessments, SOP development, and staff training.

Site Network

Partner sites spanning public hospitals, academic medical centers, and specialty clinics across Oman.

OncologyCardiovascularEndocrinologyInfectious DiseaseNeurologyRespiratoryImmunologyGastroenterology

Capabilities

5+
Hospital Partners
8+
Therapeutic Areas
15+
Certified Staff
48hrs
Response Time

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Submit a feasibility inquiry. Our team will respond within 48 hours.

Secure & Confidential

All submissions are encrypted. 48-hour response SLA guaranteed.

Feasibility Request

Submit your inquiry for clinical trial feasibility assessment in Oman.

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