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To better assist you with your request, please choose a research area provided by iNGENū CRO. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.

Clinical Trial Design

Develop study-related protocols, case report forms (CRFs) and database tools for records management.
Quality Control

Ensure products or services adhere to a set minimum standard.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Patient Recruitment

Recruit and retain patients for clinical trials.
Site Selection

Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Case Report Monitoring & Auditing

Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
Investigator Recruitment

Enlist clinical research experts to assist in investigator selection, recruitment monitoring and database evaluation.
Regulatory Affairs Consulting

Receive assistance ensuring compliance with regulatory requirements.
Phase 1-3 Studies

Design phase 1-3 studies that seek to identify if a drug is safe, effective, and more efficient than other available treatments on the market.
Regulatory Operations

Ensure that all specific regulatory documents are published and properly organized before submission.
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