Experienced in pharmaceutical, biologic, medical device regulatory writing, the Criterion Edge team of specialized medical writers provides our clients with the flexibility needed to meet your critical writing deliverables. Our team specializes in the development and writing of Clinical Evaluation Reports for Class I, II, and III Medical Devices. With over four decades of direct industry experience, Criterion Edge is at the intersection of skill and scalability in Regulatory Writing Services. Already have an internal team? We can support your team in any capacity. Criterion Edge also provides services for Medical Safety Support.
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