Criterion Edge and Alexavi Healthcare have teamed up to provide complete lifecycle coverage and support to medical device, in-vitro diagnostic device, and pharma/biopharma companies.
Take advantage of our unparalleled regulatory expertise, proactive collaboration, uncompromising quality, and scalable solutions tailored to meet your evolving needs.
Achieve high-quality, compliant written deliverables with our deep bench of seasoned regulatory writers and medical librarians that have specialized degrees and extensive therapeutic area knowledge.
Experience our collaborative and partner-centric approach that blends your insights with our expert writing services to produce tailored regulatory documentation.
Reduce revisions and accelerate approval timelines with our rigorous quality control processes and experienced writers that produce superior drafts that meet global regulatory standards.
Take advantage of our flexible staffing model that scales to match project demands, providing the regulatory experts required to meet your evolving needs without delay.
From the earliest stages of product conceptualization to regulatory writing and post-market compliance, Criterion Edge + Alexavi cover and support the entire product lifecycle.
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