Criterion Edge provides best in class regulatory writing services for the Medical Device, Biopharma/Pharma, and In-Vitro Diagnostic Device industries.
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.
Whether you’re looking for a regulatory, medical and/or scientific writing partner; or just want to price shop a potential project – we’d love to connect. Fill out the form and someone from our team will be in touch within one business day.
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