Medical Device Preclinical Safety & Feasibility Testing
From testing configurations and component compatibility to ensuring safety and an adequate handling profile, GLOBAL can assist you in preclinical study design, execution and reporting
Medical Device
Preclinical Safety and Feasibility Testing
Medical Device Preclinical Safety and Feasibility Testing services offered by GLOBAL include:
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Medical device preclinical study design
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Preclinical testing lab selection and management
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On-site preclinical study support at the lab
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Preclinical study reporting and regulatory writing
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Physician training labs
Why Choose GLOBAL for Medical Device
Preclinical Safety and Feasibility Testing
The GLOBAL preclinical team is led by a US licensed veterinarian with decades of experience in medical device preclinical study design, execution and reporting. With close connections to major testing labs worldwide, we are well situated to find reliable and cost-effective solutions for your R&D needs.
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Preclinical Safety testing is an important phase of your medical device development, from testing configurations and component compatibility to ensuring safety and an adequate handling profile. GLOBAL can assist you in preclinical study design, execution and reporting for your regulatory submissions and requirements that precede your clinical trial phase. Ensuring proper execution is critical during this phase; GLOBAL can provide on-site support to monitor protocol adherence and proper device handling.
Once your device is closer to final configuration or near market, you may want to validate handling characteristics with your end users: physicians. GLOBAL can facilitate scheduling of physician feedback/training labs to provide feedback for your R&D and marketing teams.