San Luis Obispo, California: July 23, 2022, Life Sciences Review named Criterion Edge the “Company of the Year” in its annual listing of leading service providers that are transforming the regulatory business landscape. The award noted Criterion Edge’s comprehensive expertise in regulatory writing, outstanding flexibility in meeting client demands, and best-in-class processes and quality control when awarding the company it’s top recognition.
“We are honored to receive this award from Life Sciences Review, recognizing the excellence of the entire Criterion Edge team,” commented Laurie Mitchell, President. “Our writers are experts at clearly presenting complex data and analysis, and consistently produce rigorous, well-written reports and documents that not only meet applicable regulatory requirements, but also exceed our client’s expectations."
“Criterion Edge's team approach and significant experience in MDR and IVDR, combined with their rigorous quality and training programs has led to significant success,” noted Max Wilson, Editor at Life Sciences Review. “The company provides writing services to some of the top names in the medical device, in vitro diagnostic (IVD) and biotech industries.”
“Together with our project management, regulatory consulting and systematic literature review support teams," continued Ms. Mitchell. “Criterion Edge clients have access to best-in-class full-service writing, regulatory consultation, and systematic literature review services to help their organization navigate and comply with the current, rapidly evolving regulatory landscape. This award shows that our best-practice approach to writing regulatory, scientific, and marketing documents has resonated well in the market.”
The “Company of the Year” award was published this fall in a special edition of Life Sciences Review. The magazine’s editorial panel selected Criterion Edge as the “Company of the Year,” after selecting and interviewing the 10 finalists also included in the publication. “The Company of the Year Award recognizes a business that offers more than just services. It has its clients’ backs and shares their goals,” added Mr. Wilson.
Companies need to keep budget for medical writing in check while thoroughly complying with regional regulations and rigorous standards. Outsourcing regulatory and medical writing tasks opens your medical writing team to greater flexibility. Criterion Edge has specialized medical writing expertise, which includes direct scientific, clinical and laboratory writing experience. Our medical writing experts are scientists, researchers, physicians, and healthcare providers.
Read CE President Laurie Mitchell's profile published in the special edition of Life Sciences Review Magazine to see why we were named the best of the best.Read more
Criterion Edge is a focused service provider, delivering medical, scientific, and regulatory writing and consulting services to the pharmaceutical, medical device, and in vitro device industries. The company's expertise in regulatory writing and consulting, acquired through decades of industry experience, utilizes best practice processes, produces superior deliverables, and provides budget, resource, and timeline flexibility for clients. Criterion Edge empowers companies to deliver superior health care solutions.
Criterion Edge management has over 40 years of industry experience in the pharmaceutical, medical device, and in vitro diagnostics regulatory space.
All our medical writers and quality-control experts are trained to industry best practices, and kept current on changing global regulatory guidelines.
We have developed state-of-the-art templates, tools and analysis practices to quickly identify the root cause of quality issues, and implement solutions for our clients.