Clinical Studies

Clinical Performance Studies

Our goal is to demonstrate the ability of your medical device to achieve its intended purpose and how it performs in routine clinical practice (i.e., “the real world”)

clinical trial samples being tested

Study Details

Include study description and identifier, product identifier, IFU version, initiation and completion dates.

Findings & Conclusion

Provides a summary of the study results and explain how the study objectives were achieved.

Protocol & Report

Includes the study objectives, design, methodology, and collected data.

How We Work

Invitrox conducts all testing services professionally, accurately, and promptly. Additionally, all services comply with applicable state and federal testing requirements for clinical reference laboratories.

Services must be conducted in-house at the Invitrox testing facilities to ensure accurate identification of testing location. Invitrox cannot subcontract services to third-party reference laboratories without prior written consent from the client.

Invitrox is responsible for maintaining all necessary licenses, permits, accreditations, and certifications (collectively referred to as Required Approvals) for itself and its employees throughout the agreement term. These approvals must meet the standards set by applicable laws and accreditation agencies.

Invitrox is responsible for maintaining all necessary licenses, permits, accreditations, and certifications (collectively referred to as Required Approvals) for itself and its employees throughout the agreement term. These approvals must meet the standards set by applicable laws and accreditation agencies.

Contact Invitrox Staff